JSON

Strain sc|0019926

Name

Bacillus cereus

Strain numbers

ATCC 14579 = BCRC 10603 = CCM 2010 = CCRC 10603 = CCUG 7414 = CIP 66.24 = DSM 31 = HAMBI 1887 = IAM 12605 = IFO 15305 = JCM 2152 = LMG 6923 = NBRC 15305 = NCCB 75008 = NCDO 1771 = NCFB 1771 = NCIB 9373 = NCIMB 9373 = NCTC 2599 = NRRL B-3711 = VKM B-504

StrainInfo: SI-ID 1101 T

Taxon
Bacillus cereus
Sample
Fly (JP)
Cultures (37)
LMG 6923 = ATCC 14579 = CCM 2010 = CCUG 7414 = CECT 148 = DSM 31 = IAM 12605 = JCM 2152 = NCFB 1771 = NCIB 9373 = NCTC 2599 = NRRL B-3711 = IFO 15305 = NCIMB 9373 = NCDO1771 = CIP 66.24 = LMD 75.8 = CCRC 11026 = VTT E-93143 = CECT 5050 = KCTC 3624 = NBRC 15305 = NCCB 75008 = BCRC 10603 = HAMBI 1887 = BCRC 11026 = CCT 0198 = CCT 0240 = CCT 1300 = ICMP 12436 = ICMP 12370 = IAM 14174 = NCAIM B.02078 = NRRL 3711 = VKM B-504 = CGMCC 1.3760 = CCRC 10603
Other Designations (19)
Ford 13 = FIRDI 603 = Logan B0002 = OUT 8406 = Gibson 971 = CCEB 625 = LMG 6923T QC 11/98 = LMG 6923 QC oorspr = LMG 6923T QC 9/01 = LMG6923T QC 11/03 = CER001 = W.W. Ford 13 = DSMZ 31 = RA2 = Gibson = T. Gibson 971 = CCTM La 3674 = RA10 = 971
Sequences (94)
Associated Publications (268)
  • DOI: 10.4315/0362-028x-65.12.1924
    Loss CR, Hotchkiss JH (2002). Effect of dissolved carbon dioxide on thermal inactivation of microorganisms in milk.
  • DOI: 10.1128/JB.186.10.3108-3116.2004
    Espinasse S, Gohar M, Lereclus D, Sanchis V (2004). An extracytoplasmic-function sigma factor is involved in a pathway controlling beta-exotoxin I production in Bacillus thuringiensis subsp. thuringiensis strain 407-1.
  • DOI: 10.1007/s11274-014-1792-z
    Euanorasetr J, Intra B, Mongkol P, Chankhamhaengdecha S, Tuchinda P, Mori M, Shiomi K, Nihira T, Panbangred W (2014). Spirotetronate antibiotics with anti-Clostridium activity from Actinomadura sp. 2EPS.
  • DOI: 10.1016/j.micpath.2016.06.018
    Ben Taheur F, Kouidhi B, Fdhila K, Elabed H, Ben Slama R, Mahdouani K, Bakhrouf A, Chaieb K (2016). Anti-bacterial and anti-biofilm activity of probiotic bacteria against oral pathogens.
  • DOI: 10.1371/journal.pone.0162433
    Abfalter CM, Schonauer E, Ponnuraj K, Huemer M, Gadermaier G, Regl C, Briza P, Ferreira F, Huber CG, Brandstetter H, Posselt G, Wessler S (2016). Cloning, Purification and Characterization of the Collagenase ColA Expressed by Bacillus cereus ATCC 14579.
  • DOI: 10.1021/acs.jafc.6b03334
    Ishag AE, Abdelbagi AO, Hammad AM, Elsheikh EA, Elsaid OE, Hur JH, Laing MD (2016). Biodegradation of Chlorpyrifos, Malathion, and Dimethoate by Three Strains of Bacteria Isolated from Pesticide-Polluted Soils in Sudan.
  • DOI: 10.3390/ijms21155198
    Wang Y, de Boer R, Vischer N, van Haastrecht P, Setlow P, Brul S (2020). Visualization of Germination Proteins in Putative Bacillus cereus Germinosomes.
  • DOI: 10.3390/molecules26092635
    Al-Mohammadi AR, Ibrahim RA, Moustafa AH, Ismaiel AA, Abou Zeid A, Enan G (2021). Chemical Constitution and Antimicrobial Activity of Kefir Fermented Beverage.
  • DOI: 10.1007/s11356-022-22801-7
    Thiour-Mauprivez C, Dayan FE, Terol H, Devers M, Calvayrac C, Martin-Laurent F, Barthelmebs L (2022). Assessing the effects of beta-triketone herbicides on HPPD from environmental bacteria using a combination of in silico and microbiological approaches.
  • DOI: 10.1016/j.ijbiomac.2023.127628
    Hossain MM, Rajia S, Ohkawa M, Yoshimoto S, Fujii Y, Kawsar SMA, Ozeki Y, Hasan I (2023). Physicochemical properties and antimicrobial activities of MytiLec-1, a member from the mytilectin family of mussels.
  • DOI: 10.1016/j.ijfoodmicro.2024.110709
    Khanal S, Kim TD, Begyn K, Duverger W, Kramer G, Brul S, Rajkovic A, Devlieghere F, Heyndrickx M, Schymkowitz J, Rousseau F, Broussolle V, Michiels C, Aertsen A (2024). Mechanistic insights into the adaptive evolvability of spore heat resistance in Bacillus cereus sensu lato.
  • DOI: 10.1128/jb.174.11.3750-3756.1992
    Carlson CR, Gronstad A, Kolsto AB (1992). Physical maps of the genomes of three Bacillus cereus strains.
  • Lau TM, Chan KY (1984). Physiological responses of Bacillus species to concanavalin A. 2. Effect on growth, oxygen uptake, enzyme activities and intracellular cyclic guanosine 3',5'-monophosphate level of B. cereus ATCC 14579.
  • DOI: 10.1007/BF00410891
    Cerniglia CE, Freeman JP, Evans FE (1984). Evidence for an arene oxide-NIH shift pathway in the transformation of naphthalene to 1-naphthol by Bacillus cereus.
  • DOI: 10.1007/BF00145422
    Matar GM, Slieman TA, Nabbut NH (1996). Subtyping of Bacillus cereus by total cell protein patterns and arbitrary primer polymerase chain reaction.
  • Gruzina TG, Balakina MN, Karamushka VI, Stepura LG, Ul'berg ZR (1997). [Bacterial cell membrane ATPase in assessing heavy metal toxicity].
  • DOI: 10.1111/j.1574-6968.1997.tb12641.x
    Okstad OA, Gronstad A, Lindback T, Kolsto AB (1997). Insertional inactivation of a Tet(K)/Tet(L) like transporter does not eliminate tetracycline resistance in Bacillus cereus.
  • DOI: 10.1128/IAI.66.5.2163-2169.1998
    Leonard C, Zekri O, Mahillon J (1998). Integrated physical and genetic mapping of Bacillus cereus and other gram-positive bacteria based on IS231A transposition vectors.
  • DOI: 10.1046/j.1365-2672.1998.00460.x
    Raso J, Barbosa-Canovas G, Swanson BG (1998). Sporulation temperature affects initiation of germination and inactivation by high hydrostatic pressure of Bacillus cereus.
  • DOI: 10.1128/IAI.66.10.4895-4902.1998
    Kotiranta A, Haapasalo M, Kari K, Kerosuo E, Olsen I, Sorsa T, Meurman JH, Lounatmaa K (1998). Surface structure, hydrophobicity, phagocytosis, and adherence to matrix proteins of Bacillus cereus cells with and without the crystalline surface protein layer.
  • DOI: 10.1099/00221287-145-11-3139
    Lindback T, Okstad OA, Rishovd AL, Kolsto AB (1999). Insertional inactivation of hblC encoding the L2 component of Bacillus cereus ATCC 14579 haemolysin BL strongly reduces enterotoxigenic activity, but not the haemolytic activity against human erythrocytes.
  • DOI: 10.1021/ac990832j
    Jarman KH, Cebula ST, Saenz AJ, Petersen CE, Valentine NB, Kingsley MT, Wahl KL (2000). An algorithm for automated bacterial identification using matrix-assisted laser desorption/ionization mass spectrometry.
  • DOI: 10.1111/j.1574-6968.2000.tb09294.x
    Celandroni F, Ghelardi E, Pastore M, Lupetti A, Kolsto AB, Senesi S (2000). Characterization of the chemotaxis fli Y and che A genes in Bacillus cereus.
  • DOI: 10.1099/00221287-146-11-2825
    Salamitou S, Ramisse F, Brehelin M, Bourguet D, Gilois N, Gominet M, Hernandez E, Lereclus D (2000). The plcR regulon is involved in the opportunistic properties of Bacillus thuringiensis and Bacillus cereus in mice and insects.
  • DOI: 10.1002/1521-3803(20001001)44:5<364::AID-FOOD364>3.0.CO;2-0
    Enan G (2000). Inhibition of Bacillus cereus ATCC 14579 by plantaricin UG1 in vitro and in food.
  • DOI: 10.1128/AEM.68.7.3486-3495.2002
    Periago PM, van Schaik W, Abee T, Wouters JA (2002). Identification of proteins involved in the heat stress response of Bacillus cereus ATCC 14579.
  • DOI: 10.1002/1615-9861(200206)2:6<784::AID-PROT784>3.0.CO;2-R
    Gohar M, Okstad OA, Gilois N, Sanchis V, Kolsto AB, Lereclus D (2002). Two-dimensional electrophoresis analysis of the extracellular proteome of Bacillus cereus reveals the importance of the PlcR regulon.
  • Wang L, Chen Y, Mahillion J, Yu Z (2001). [Transcriptional activator PlcR regulate the expression of multiple genes in Bacillus cereus].
  • DOI: 10.1038/nature01582
    Ivanova N, Sorokin A, Anderson I, Galleron N, Candelon B, Kapatral V, Bhattacharyya A, Reznik G, Mikhailova N, Lapidus A, Chu L, Mazur M, Goltsman E, Larsen N, D'Souza M, Walunas T, Grechkin Y, Pusch G, Haselkorn R, Fonstein M, Ehrlich SD, Overbeek R, Kyrpides N (2003). Genome sequence of Bacillus cereus and comparative analysis with Bacillus anthracis.
  • DOI: 10.1128/JB.185.11.3373-3378.2003
    Todd SJ, Moir AJ, Johnson MJ, Moir A (2003). Genes of Bacillus cereus and Bacillus anthracis encoding proteins of the exosporium.
  • DOI: 10.1007/s00253-003-1256-0
    Agbessi S, Beausejour J, Dery C, Beaulieu C (2003). Antagonistic properties of two recombinant strains of Streptomyces melanosporofaciens obtained by intraspecific protoplast fusion.
  • DOI: 10.1128/JB.186.2.316-325.2004
    van Schaik W, Tempelaars MH, Wouters JA, de Vos WM, Abee T (2004). The alternative sigma factor sigmaB of Bacillus cereus: response to stress and role in heat adaptation.
  • DOI: 10.1093/nar/gkh258
    Rasko DA, Ravel J, Okstad OA, Helgason E, Cer RZ, Jiang L, Shores KA, Fouts DE, Tourasse NJ, Angiuoli SV, Kolonay J, Nelson WC, Kolsto AB, Fraser CM, Read TD (2004). The genome sequence of Bacillus cereus ATCC 10987 reveals metabolic adaptations and a large plasmid related to Bacillus anthracis pXO1.
  • DOI: 10.1099/mic.0.26870-0
    Candelon B, Guilloux K, Ehrlich SD, Sorokin A (2004). Two distinct types of rRNA operons in the Bacillus cereus group.
  • DOI: 10.1046/j.1365-2672.2003.02139.x
    Risoen PA, Ronning P, Hegna IK, Kolsto AB (2004). Characterization of a broad range antimicrobial substance from Bacillus cereus.
  • DOI: 10.1128/AEM.70.4.2514-2519.2004
    de Vries YP, Hornstra LM, de Vos WM, Abee T (2004). Growth and sporulation of Bacillus cereus ATCC 14579 under defined conditions: temporal expression of genes for key sigma factors.
  • DOI: 10.1128/JB.186.13.4100-4109.2004
    van Schaik W, Zwietering MH, de Vos WM, Abee T (2004). Identification of sigmaB-dependent genes in Bacillus cereus by proteome and in vitro transcription analysis.
  • DOI: 10.1099/mic.0.26975-0
    Fagerlund A, Ween O, Lund T, Hardy SP, Granum PE (2004). Genetic and functional analysis of the cytK family of genes in Bacillus cereus.
  • DOI: 10.1099/mic.0.27069-0
    Brillard J, Lereclus D (2004). Comparison of cytotoxin cytK promoters from Bacillus cereus strain ATCC 14579 and from a B. cereus food-poisoning strain.
  • DOI: 10.1128/JB.186.22.7714-7725.2004
    Okstad OA, Tourasse NJ, Stabell FB, Sundfaer CK, Egge-Jacobsen W, Risoen PA, Read TD, Kolsto AB (2004). The bcr1 DNA repeat element is specific to the Bacillus cereus group and exhibits mobile element characteristics.
  • DOI: 10.1128/AEM.71.2.774-781.2005
    Hornstra LM, de Vries YP, de Vos WM, Abee T, Wells-Bennik MH (2005). gerR, a novel ger operon involved in L-alanine- and inosine-initiated germination of Bacillus cereus ATCC 14579.
  • DOI: 10.1128/JB.187.6.1966-1973.2005
    Verheust C, Fornelos N, Mahillon J (2005). GIL16, a new gram-positive tectiviral phage related to the Bacillus thuringiensis GIL01 and the Bacillus cereus pBClin15 elements.
  • DOI: 10.1128/AEM.71.6.3248-3254.2005
    de Vries YP, Atmadja RD, Hornstra LM, de Vos WM, Abee T (2005). Influence of glutamate on growth, sporulation, and spore properties of Bacillus cereus ATCC 14579 in defined medium.
  • DOI: 10.1128/JB.187.15.5437-5451.2005
    Tourasse NJ, Stabell FB, Reiter L, Kolsto AB (2005). Unusual group II introns in bacteria of the Bacillus cereus group.
  • DOI: 10.1139/w04-132
    Rosenfeld E, Duport C, Zigha A, Schmitt P (2005). Characterization of aerobic and anaerobic vegetative growth of the food-borne pathogen Bacillus cereus F4430/73 strain.
  • DOI: 10.1128/AEM.71.10.6427-6430.2005
    van Schaik W, Zwietering MH, de Vos WM, Abee T (2005). Deletion of the sigB gene in Bacillus cereus ATCC 14579 leads to hydrogen peroxide hyperresistance.
  • DOI: 10.1128/AEM.72.1.44-53.2006
    Hornstra LM, de Vries YP, Wells-Bennik MH, de Vos WM, Abee T (2006). Characterization of germination receptors of Bacillus cereus ATCC 14579.
  • DOI: 10.1111/j.1365-2672.2006.02822.x
    Gray EJ, Lee KD, Souleimanov AM, Di Falco MR, Zhou X, Ly A, Charles TC, Driscoll BT, Smith DL (2006). A novel bacteriocin, thuricin 17, produced by plant growth promoting rhizobacteria strain Bacillus thuringiensis NEB17: isolation and classification.
  • DOI: 10.1128/JB.188.9.3382-3390.2006
    Han CS, Xie G, Challacombe JF, Altherr MR, Bhotika SS, Brown N, Bruce D, Campbell CS, Campbell ML, Chen J, Chertkov O, Cleland C, Dimitrijevic M, Doggett NA, Fawcett JJ, Glavina T, Goodwin LA, Green LD, Hill KK, Hitchcock P, Jackson PJ, Keim P, Kewalramani AR, Longmire J, Lucas S, Malfatti S, McMurry K, Meincke LJ, Misra M, Moseman BL, Mundt M, Munk AC, Okinaka RT, Parson-Quintana B, Reilly LP, Richardson P, Robinson DL, Rubin E, Saunders E, Tapia R, Tesmer JG, Thayer N, Thompson LS, Tice H, Ticknor LO, Wills PL, Brettin TS, Gilna P (2006). Pathogenomic sequence analysis of Bacillus cereus and Bacillus thuringiensis isolates closely related to Bacillus anthracis.
  • DOI: 10.1128/AEM.72.5.3746-3749.2006
    Hornstra LM, de Vries YP, de Vos WM, Abee T (2006). Influence of sporulation medium composition on transcription of ger operons and the germination response of spores of Bacillus cereus ATCC 14579.
  • DOI: 10.1111/j.1574-6968.2006.00289.x
    Hajaij-Ellouze M, Fedhila S, Lereclus D, Nielsen-LeRoux C (2006). The enhancin-like metalloprotease from the Bacillus cereus group is regulated by the pleiotropic transcriptional activator PlcR but is not essential for larvicidal activity.
  • DOI: 10.1016/j.mimet.2006.05.005
    Turgeon N, Laflamme C, Ho J, Duchaine C (2006). Elaboration of an electroporation protocol for Bacillus cereus ATCC 14579.
  • DOI: 10.1128/AEM.03076-05
    Vilain S, Luo Y, Hildreth MB, Brozel VS (2006). Analysis of the life cycle of the soil saprophyte Bacillus cereus in liquid soil extract and in soil.
  • DOI: 10.1128/AEM.00573-06
    Hsueh YH, Somers EB, Lereclus D, Wong AC (2006). Biofilm formation by Bacillus cereus is influenced by PlcR, a pleiotropic regulator.
  • DOI: 10.1074/jbc.M605768200
    Choudhury B, Leoff C, Saile E, Wilkins P, Quinn CP, Kannenberg EL, Carlson RW (2006). The structure of the major cell wall polysaccharide of Bacillus anthracis is species-specific.
  • DOI: 10.1016/j.bbrc.2006.07.055
    Wilson MK, Abergel RJ, Raymond KN, Arceneaux JE, Byers BR (2006). Siderophores of Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis.
  • DOI: 10.1007/s00203-006-0137-1
    Thomassin S, Jobin MP, Schmitt P (2006). The acid tolerance response of Bacillus cereus ATCC14579 is dependent on culture pH, growth rate and intracellular pH.
  • DOI: 10.1128/AEM.00780-06
    den Besten HM, Mataragas M, Moezelaar R, Abee T, Zwietering MH (2006). Quantification of the effects of salt stress and physiological state on thermotolerance of Bacillus cereus ATCC 10987 and ATCC 14579.
  • DOI: 10.1111/j.1365-2958.2006.05362.x
    Fedhila S, Daou N, Lereclus D, Nielsen-LeRoux C (2006). Identification of Bacillus cereus internalin and other candidate virulence genes specifically induced during oral infection in insects.
  • DOI: 10.1016/j.gene.2006.09.010
    Kalia VC, Lal S, Cheema S (2006). Insight in to the phylogeny of polyhydroxyalkanoate biosynthesis: horizontal gene transfer.
  • DOI: 10.1128/AEM.01781-06
    Wijman JG, de Leeuw PP, Moezelaar R, Zwietering MH, Abee T (2007). Air-liquid interface biofilms of Bacillus cereus: formation, sporulation, and dispersion.
  • DOI: 10.1016/j.ijfoodmicro.2007.02.012
    Hornstra LM, de Leeuw PL, Moezelaar R, Wolbert EJ, de Vries YP, de Vos WM, Abee T (2007). Germination of Bacillus cereus spores adhered to stainless steel.
  • DOI: 10.1128/JB.00313-07
    van Schaik W, van der Voort M, Molenaar D, Moezelaar R, de Vos WM, Abee T (2007). Identification of the sigmaB regulon of Bacillus cereus and conservation of sigmaB-regulated genes in low-GC-content gram-positive bacteria.
  • DOI: 10.1002/pmic.200600502
    Gilois N, Ramarao N, Bouillaut L, Perchat S, Aymerich S, Nielsen-Leroux C, Lereclus D, Gohar M (2007). Growth-related variations in the Bacillus cereus secretome.
  • DOI: 10.1128/JB.00239-07
    Kristoffersen SM, Ravnum S, Tourasse NJ, Okstad OA, Kolsto AB, Davies W (2007). Low concentrations of bile salts induce stress responses and reduce motility in Bacillus cereus ATCC 14579 [corrected].
  • DOI: 10.1128/AEM.00404-07
    den Besten HM, Ingham CJ, van Hylckama Vlieg JE, Beerthuyzen MM, Zwietering MH, Abee T (2007). Quantitative analysis of population heterogeneity of the adaptive salt stress response and growth capacity of Bacillus cereus ATCC 14579.
  • DOI: 10.1186/1471-2180-7-52
    Brillard J, Lereclus D (2007). Characterization of a small PlcR-regulated gene co-expressed with cereolysin O.
  • DOI: 10.1128/AEM.00690-07
    Hsueh YH, Somers EB, Lereclus D, Ghelardi E, Wong AC (2007). Biosurfactant production and surface translocation are regulated by PlcR in Bacillus cereus ATCC 14579 under low-nutrient conditions.
  • DOI: 10.4315/0362-028x-70.10.2346
    Faille C, Tauveron G, Le Gentil-Lelievre C, Slomianny C (2007). Occurrence of Bacillus cereus spores with a damaged exosporium: consequences on the spore adhesion on surfaces of food processing lines.
  • DOI: 10.1128/JB.01292-07
    Leoff C, Saile E, Sue D, Wilkins P, Quinn CP, Carlson RW, Kannenberg EL (2007). Cell wall carbohydrate compositions of strains from the Bacillus cereus group of species correlate with phylogenetic relatedness.
  • DOI: 10.1111/j.1462-2920.2007.01404.x
    Mols M, de Been M, Zwietering MH, Moezelaar R, Abee T (2007). Metabolic capacity of Bacillus cereus strains ATCC 14579 and ATCC 10987 interlinked with comparative genomics.
  • DOI: 10.1016/j.fm.2007.08.002
    Gounina-Allouane R, Broussolle V, Carlin F (2007). Influence of the sporulation temperature on the impact of the nutrients inosine and l-alanine on Bacillus cereus spore germination.
  • DOI: 10.1186/1471-2180-8-62
    van der Voort M, Kuipers OP, Buist G, de Vos WM, Abee T (2008). Assessment of CcpA-mediated catabolite control of gene expression in Bacillus cereus ATCC 14579.
  • DOI: 10.1007/s00253-008-1473-7
    Lee SH, Park SJ, Lee SY, Hong SH (2008). Biosynthesis of enantiopure (S)-3-hydroxybutyric acid in metabolically engineered Escherichia coli.
  • DOI: 10.1155/2008/451930
    Zhang R, Zhang CT (2008). Accurate localization of the integration sites of two genomic islands at single-nucleotide resolution in the genome of Bacillus cereus ATCC 10987.
  • DOI: 10.1371/journal.pone.0002793
    Gohar M, Faegri K, Perchat S, Ravnum S, Okstad OA, Gominet M, Kolsto AB, Lereclus D (2008). The PlcR virulence regulon of Bacillus cereus.
  • DOI: 10.1016/j.mimet.2008.07.020
    Kumar TD, Murali HS, Batra HV (2008). Construction of a non toxic chimeric protein (L1-L2-B) of Haemolysin BL from Bacillus cereus and its application in HBL toxin detection.
  • DOI: 10.1074/jbc.M803234200
    Leoff C, Choudhury B, Saile E, Quinn CP, Carlson RW, Kannenberg EL (2008). Structural elucidation of the nonclassical secondary cell wall polysaccharide from Bacillus cereus ATCC 10987. Comparison with the polysaccharides from Bacillus anthracis and B. cereus type strain ATCC 14579 reveals both unique and common structural features.
  • DOI: 10.1186/1471-2180-8-183
    Brillard J, Susanna K, Michaud C, Dargaignaratz C, Gohar M, Nielsen-Leroux C, Ramarao N, Kolsto AB, Nguyen-the C, Lereclus D, Broussolle V (2008). The YvfTU two-component system is involved in plcR expression in Bacillus cereus.
  • DOI: 10.1111/j.1472-765X.2008.02483.x
    Stabell FB, Egge-Jacobsen W, Risoen PA, Kolsto AB, Okstad OA (2008). ORF 2 from the Bacillus cereus linear plasmid pBClin15 encodes a DNA binding protein.
  • DOI: 10.1128/AEM.02238-08
    Hornstra LM, van der Voort M, Wijnands LM, Roubos-van den Hil PJ, Abee T (2008). Role of germinant receptors in Caco-2 cell-initiated germination of Bacillus cereus ATCC 14579 endospores.
  • DOI: 10.1016/j.chembiol.2009.01.007
    Liao R, Duan L, Lei C, Pan H, Ding Y, Zhang Q, Chen D, Shen B, Yu Y, Liu W (2009). Thiopeptide biosynthesis featuring ribosomally synthesized precursor peptides and conserved posttranslational modifications.
  • DOI: 10.1128/AEM.01317-08
    Vilain S, Pretorius JM, Theron J, Brozel VS (2009). DNA as an adhesin: Bacillus cereus requires extracellular DNA to form biofilms.
  • DOI: 10.1093/glycob/cwp036
    Leoff C, Saile E, Rauvolfova J, Quinn CP, Hoffmaster AR, Zhong W, Mehta AS, Boons GJ, Carlson RW, Kannenberg EL (2009). Secondary cell wall polysaccharides of Bacillus anthracis are antigens that contain specific epitopes which cross-react with three pathogenic Bacillus cereus strains that caused severe disease, and other epitopes common to all the Bacillus cereus strains tested.
  • DOI: 10.1111/j.1365-2672.2009.04254.x
    Ouhib-Jacobs O, Lindley ND, Schmitt P, Clavel T (2009). Fructose and glucose mediates enterotoxin production and anaerobic metabolism of Bacillus cereus ATCC14579(T).
  • DOI: 10.1111/j.1365-2672.2009.04252.x
    van der Voort M, Abee T (2009). Transcriptional regulation of metabolic pathways, alternative respiration and enterotoxin genes in anaerobic growth of Bacillus cereus ATCC 14579.
  • DOI: 10.1128/AEM.02891-08
    den Besten HM, Mols M, Moezelaar R, Zwietering MH, Abee T (2009). Phenotypic and transcriptomic analyses of mildly and severely salt-stressed Bacillus cereus ATCC 14579 cells.
  • DOI: 10.1128/JB.00272-09
    Wang SW, Chen CY, Tseng JT, Liang SH, Chen SC, Hsieh C, Chen YH, Chen CC (2009). orf4 of the Bacillus cereus sigB gene cluster encodes a general stress-inducible Dps-like bacterioferritin.
  • DOI: 10.1007/s12010-009-8685-x
    Yao T, Xu L, Ying H, Huang H, Yan M (2009). The catalytic property of 3-hydroxyisobutyrate dehydrogenase from Bacillus cereus on 3-hydroxypropionate.
  • DOI: 10.1016/j.ejmech.2009.06.021
    Barbuceanu SF, Almajan GL, Saramet I, Draghici C, Tarcomnicu AI, Bancescu G (2009). Synthesis, characterization and evaluation of antibacterial activity of some thiazolo[3,2-b][1,2,4]triazole incorporating diphenylsulfone moieties.
  • DOI: 10.1016/j.ijfoodmicro.2009.09.002
    Mols M, Pier I, Zwietering MH, Abee T (2009). The impact of oxygen availability on stress survival and radical formation of Bacillus cereus.
  • DOI: 10.1016/j.ijfoodmicro.2009.09.027
    Mols M, van Kranenburg R, Tempelaars MH, van Schaik W, Moezelaar R, Abee T (2009). Comparative analysis of transcriptional and physiological responses of Bacillus cereus to organic and inorganic acid shocks.
  • DOI: 10.1186/1471-2180-9-227
    Grande Burgos MJ, Kovacs AT, Mironczuk AM, Abriouel H, Galvez A, Kuipers OP (2009). Response of Bacillus cereus ATCC 14579 to challenges with sublethal concentrations of enterocin AS-48.
  • DOI: 10.1111/j.1365-2672.2009.04637.x
    Roubos-van den Hil PJ, Dalmas E, Nout MJ, Abee T (2009). Soya bean tempe extracts show antibacterial activity against Bacillus cereus cells and spores.
  • DOI: 10.1128/AEM.01372-09
    den Besten HM, Garcia D, Moezelaar R, Zwietering MH, Abee T (2009). Direct-imaging-based quantification of Bacillus cereus ATCC 14579 population heterogeneity at a low incubation temperature.
  • DOI: 10.1111/j.1462-2920.2009.02132.x
    Mols M, van Kranenburg R, van Melis CC, Moezelaar R, Abee T (2010). Analysis of acid-stressed Bacillus cereus reveals a major oxidative response and inactivation-associated radical formation.
  • DOI: 10.1016/j.ijfoodmicro.2010.01.028
    van der Voort M, Garcia D, Moezelaar R, Abee T (2010). Germinant receptor diversity and germination responses of four strains of the Bacillus cereus group.
  • DOI: 10.1128/AEM.02348-09
    Brillard J, Jehanno I, Dargaignaratz C, Barbosa I, Ginies C, Carlin F, Fedhila S, Nguyen-the C, Broussolle V, Sanchis V (2010). Identification of Bacillus cereus genes specifically expressed during growth at low temperatures.
  • DOI: 10.1128/AEM.03003-09
    Ceragioli M, Mols M, Moezelaar R, Ghelardi E, Senesi S, Abee T (2010). Comparative transcriptomic and phenotypic analysis of the responses of Bacillus cereus to various disinfectant treatments.
  • DOI: 10.1111/j.1574-6968.2010.01953.x
    Broussolle V, Pandiani F, Haddad N, Michaud C, Carlin F, Nguyen-the C, Brillard J (2010). Insertional mutagenesis reveals genes involved in Bacillus cereus ATCC 14579 growth at low temperature.
  • DOI: 10.1128/AEM.00150-10
    den Besten HM, van der Mark EJ, Hensen L, Abee T, Zwietering MH (2010). Quantification of the effect of culturing temperature on salt-induced heat resistance of bacillus species.
  • DOI: 10.1021/ja102339q
    Bowers AA, Acker MG, Koglin A, Walsh CT (2010). Manipulation of thiocillin variants by prepeptide gene replacement: structure, conformation, and activity of heterocycle substitution mutants.
  • DOI: 10.1111/j.1742-4658.2010.07691.x
    Deli A, Koutsioulis D, Fadouloglou VE, Spiliotopoulou P, Balomenou S, Arnaouteli S, Tzanodaskalaki M, Mavromatis K, Kokkinidis M, Bouriotis V (2010). LmbE proteins from Bacillus cereus are de-N-acetylases with broad substrate specificity and are highly similar to proteins in Bacillus anthracis.
  • DOI: 10.1002/jobm.200900348
    Gracias KS, McKillip JL (2011). Triplex PCR-based detection of enterotoxigenic Bacillus cereus ATCC 14579 in nonfat dry milk.
  • DOI: 10.1128/AEM.00782-10
    Pandiani F, Brillard J, Bornard I, Michaud C, Chamot S, Nguyen-the C, Broussolle V (2010). Differential involvement of the five RNA helicases in adaptation of Bacillus cereus ATCC 14579 to low growth temperatures.
  • DOI: 10.1111/j.1751-7915.2009.00142.x
    Grosse S, Bergeron H, Imura A, Boyd J, Wang S, Kubota K, Miyadera A, Sulea T, Lau PC (2009). Nature versus nurture in two highly enantioselective esterases from Bacillus cereus and Thermoanaerobacter tengcongensis.
  • DOI: 10.1111/j.1751-7915.2008.00023.x
    Mironczuk AM, Kovacs AT, Kuipers OP (2008). Induction of natural competence in Bacillus cereus ATCC14579.
  • DOI: 10.1128/AEM.02520-10
    van Melis CC, Nierop Groot MN, Abee T (2011). Impact of sorbic acid on germinant receptor-dependent and -independent germination pathways in Bacillus cereus.
  • DOI: 10.1016/j.fm.2010.04.005
    van Melis CC, Nierop Groot MN, Tempelaars MH, Moezelaar R, Abee T (2010). Characterization of germination and outgrowth of sorbic acid-stressed Bacillus cereus ATCC 14579 spores: phenotype and transcriptome analysis.
  • DOI: 10.1016/j.fm.2010.09.003
    Senouci-Rezkallah K, Schmitt P, Jobin MP (2010). Amino acids improve acid tolerance and internal pH maintenance in Bacillus cereus ATCC14579 strain.
  • DOI: 10.1128/AEM.02671-10
    Tempelaars MH, Rodrigues S, Abee T (2011). Comparative analysis of antimicrobial activities of valinomycin and cereulide, the Bacillus cereus emetic toxin.
  • DOI: 10.2436/20.1501.01.123
    Landete JM, Arena ME, Pardo I, Manca de Nadra MC, Ferrer S (2010). The role of two families of bacterial enzymes in putrescine synthesis from agmatine via agmatine deiminase.
  • DOI: 10.1016/j.mimet.2011.05.006
    Reiter L, Kolsto AB, Piehler AP (2011). Reference genes for quantitative, reverse-transcription PCR in Bacillus cereus group strains throughout the bacterial life cycle.
  • DOI: 10.1128/AEM.02872-10
    Lequette Y, Garenaux E, Tauveron G, Dumez S, Perchat S, Slomianny C, Lereclus D, Guerardel Y, Faille C (2011). Role played by exosporium glycoproteins in the surface properties of Bacillus cereus spores and in their adhesion to stainless steel.
  • DOI: 10.1128/AEM.00245-11
    Salvetti S, Faegri K, Ghelardi E, Kolsto AB, Senesi S (2011). Global gene expression profile for swarming Bacillus cereus bacteria.
  • DOI: 10.1128/AEM.02974-10
    Pandiani F, Chamot S, Brillard J, Carlin F, Nguyen-the C, Broussolle V (2011). Role of the five RNA helicases in the adaptive response of Bacillus cereus ATCC 14579 cells to temperature, pH, and oxidative stresses.
  • DOI: 10.1074/jbc.M111.249821
    Candela T, Maes E, Garenaux E, Rombouts Y, Krzewinski F, Gohar M, Guerardel Y (2011). Environmental and biofilm-dependent changes in a Bacillus cereus secondary cell wall polysaccharide.
  • DOI: 10.1371/journal.pone.0024304
    Mellegard H, Kovacs AT, Lindback T, Christensen BE, Kuipers OP, Granum PE (2011). Transcriptional responses of Bacillus cereus towards challenges with the polysaccharide chitosan.
  • DOI: 10.1128/JB.06248-11
    Xu SY, Nugent RL, Kasamkattil J, Fomenkov A, Gupta Y, Aggarwal A, Wang X, Li Z, Zheng Y, Morgan R (2011). Characterization of type II and III restriction-modification systems from Bacillus cereus strains ATCC 10987 and ATCC 14579.
  • DOI: 10.1186/1477-3155-9-49
    Babu MM, Sridhar J, Gunasekaran P (2011). Global transcriptome analysis of Bacillus cereus ATCC 14579 in response to silver nitrate stress.
  • DOI: 10.1128/AEM.06410-11
    de Sarrau B, Clavel T, Clerte C, Carlin F, Ginies C, Nguyen-The C (2012). Influence of anaerobiosis and low temperature on Bacillus cereus growth, metabolism, and membrane properties.
  • DOI: 10.1007/s00253-012-3919-1
    Wang L, Chong H, Jiang R (2012). Comparison of alkyl hydroperoxide reductase and two water-forming NADH oxidases from Bacillus cereus ATCC 14579.
  • DOI: 10.1111/j.1574-6968.2012.02562.x
    From C, van der Voort M, Abee T, Granum PE (2012). Characterization of a spore-specific protein of the Bacillus cereus group.
  • DOI: 10.1111/j.1462-2920.2012.02766.x
    Lindback T, Mols M, Basset C, Granum PE, Kuipers OP, Kovacs AT (2012). CodY, a pleiotropic regulator, influences multicellular behaviour and efficient production of virulence factors in Bacillus cereus.
  • DOI: 10.1371/journal.pone.0036720
    Simm R, Voros A, Ekman JV, Sodring M, Nes I, Kroeger JK, Saidijam M, Bettaney KE, Henderson PJ, Salkinoja-Salonen M, Kolsto AB (2012). BC4707 is a major facilitator superfamily multidrug resistance transport protein from Bacillus cereus implicated in fluoroquinolone tolerance.
  • DOI: 10.1021/ja302820x
    Bowers AA, Acker MG, Young TS, Walsh CT (2012). Generation of thiocillin ring size variants by prepeptide gene replacement and in vivo processing by Bacillus cereus.
  • DOI: 10.4014/jmb.1110.10002
    Kindoli S, Lee HA, Kim JH (2012). Properties of Bac W42, a bacteriocin produced by Bacillus subtilis W42 isolated from Cheonggukjang.
  • DOI: 10.1371/journal.pone.0041248
    Rogers TE, Ataide SF, Dare K, Katz A, Seveau S, Roy H, Ibba M (2012). A pseudo-tRNA modulates antibiotic resistance in Bacillus cereus.
  • DOI: 10.1128/AEM.02361-12
    den Besten HM, van Melis CC, Sanders JW, Nierop Groot MN, Abee T (2012). Impact of sorbic acid on germination and outgrowth heterogeneity of Bacillus cereus ATCC 14579 spores.
  • DOI: 10.1073/pnas.1210131109
    Fukushima T, Sia AK, Allred BE, Nichiporuk R, Zhou Z, Andersen UN, Raymond KN (2012). Bacillus cereus iron uptake protein fishes out an unstable ferric citrate trimer.
  • DOI: 10.1016/j.ijfoodmicro.2012.10.006
    van Melis CC, Almeida CB, Kort R, Groot MN, Abee T (2012). Germination inhibition of Bacillus cereus spores: impact of the lipophilic character of inhibiting compounds.
  • DOI: 10.1371/journal.pone.0048015
    Fibriansah G, Kovacs AT, Pool TJ, Boonstra M, Kuipers OP, Thunnissen AM (2012). Crystal structures of two transcriptional regulators from Bacillus cereus define the conserved structural features of a PadR subfamily.
  • DOI: 10.1111/jam.12096
    Ceuppens S, Timmery S, Mahillon J, Uyttendaele M, Boon N (2013). Small Bacillus cereus ATCC 14579 subpopulations are responsible for cytotoxin K production.
  • DOI: 10.1371/journal.pone.0051047
    Huillet E, Tempelaars MH, Andre-Leroux G, Wanapaisan P, Bridoux L, Makhzami S, Panbangred W, Martin-Verstraete I, Abee T, Lereclus D (2012). PlcRa, a new quorum-sensing regulator from Bacillus cereus, plays a role in oxidative stress responses and cysteine metabolism in stationary phase.
  • DOI: 10.1007/s00253-012-4654-3
    Pendyala B, Chaganti SR, Thadikamala S, Reddy Shetty P (2013). Heterologous expression of CYP102A5 variant from Bacillus cereus CYPPB-1: Validation of model for predicting drug metabolism of human P450 probe substrates.
  • DOI: 10.1128/AEM.01761-13
    Chazarreta Cifre L, Alemany M, de Mendoza D, Altabe S (2013). Exploring the biosynthesis of unsaturated fatty acids in Bacillus cereus ATCC 14579 and functional characterization of novel acyl-lipid desaturases.
  • DOI: 10.1099/mic.0.069674-0
    Voros A, Simm R, Kroeger JK, Kolsto AB (2013). Gene transcription from the linear plasmid pBClin15 leads to cell lysis and extracellular DNA-dependent aggregation of Bacillus cereus ATCC 14579 in response to quinolone-induced stress.
  • DOI: 10.1016/j.fm.2013.04.008
    de Sarrau B, Clavel T, Zwickel N, Despres J, Dupont S, Beney L, Tourdot-Marechal R, Nguyen-The C (2013). Unsaturated fatty acids from food and in the growth medium improve growth of Bacillus cereus under cold and anaerobic conditions.
  • DOI: 10.1016/j.mimet.2013.09.012
    Oltuszak-Walczak E, Walczak P (2013). PCR detection of cytK gene in Bacillus cereus group strains isolated from food samples.
  • DOI: 10.1007/s11274-013-1558-z
    Alkotaini B, Anuar N, Kadhum AA, Sani AA (2013). Isolation and identification of a new intracellular antimicrobial peptide produced by Paenibacillus alvei AN5.
  • DOI: 10.1371/journal.pone.0080175
    Drewnowska JM, Swiecicka I (2013). Eco-genetic structure of Bacillus cereus sensu lato populations from different environments in northeastern Poland.
  • Vasincu I, Apotrosoaei M, Tuchilus C, Panzariu AT, Dragostin O, Lupascu D, Profire L (2013). New derivatives of aryl-propionic acid. Synthesis and biological evaluation.
  • DOI: 10.1007/s00203-013-0946-y
    Venir E, Del Torre M, Cunsolo V, Saletti R, Musetti R, Stecchini ML (2013). Involvement of alanine racemase in germination of Bacillus cereus spores lacking an intact exosporium.
  • DOI: 10.1128/AEM.00090-14
    Diomande SE, Chamot S, Antolinos V, Vasai F, Guinebretiere MH, Bornard I, Nguyen-the C, Broussolle V, Brillard J (2014). The CasKR two-component system is required for the growth of mesophilic and psychrotolerant Bacillus cereus strains at low temperatures.
  • DOI: 10.1016/j.ijfoodmicro.2014.02.015
    van Melis CC, den Besten HM, Nierop Groot MN, Abee T (2014). Quantification of the impact of single and multiple mild stresses on outgrowth heterogeneity of Bacillus cereus spores.
  • DOI: 10.1111/1750-3841.12387
    Han KI, Patnaik BB, Kim YH, Kwon HJ, Han YS, Han MD (2014). Isolation and characterization of chitinase-producing Bacillus and Paenibacillus strains from salted and fermented shrimp, Acetes japonicus.
  • DOI: 10.1371/journal.pone.0103326
    Voros A, Simm R, Slamti L, McKay MJ, Hegna IK, Nielsen-LeRoux C, Hassan KA, Paulsen IT, Lereclus D, Okstad OA, Molloy MP, Kolsto AB (2014). SecDF as part of the Sec-translocase facilitates efficient secretion of Bacillus cereus toxins and cell wall-associated proteins.
  • DOI: 10.1371/journal.pone.0107354
    Laouami S, Clair G, Armengaud J, Duport C (2014). Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
  • DOI: 10.1007/s10482-014-0285-2
    Tagawa Y (2014). Isolation and characterization of flagellar filaments from Bacillus cereus ATCC 14579.
  • DOI: 10.1074/jbc.M114.614917
    Hwang S, Li Z, Bar-Peled Y, Aronov A, Ericson J, Bar-Peled M (2014). The biosynthesis of UDP-d-FucNAc-4N-(2)-oxoglutarate (UDP-Yelosamine) in Bacillus cereus ATCC 14579: Pat and Pyl, an aminotransferase and an ATP-dependent Grasp protein that ligates 2-oxoglutarate to UDP-4-amino-sugars.
  • DOI: 10.1128/JB.02125-14
    Han H, Sullivan T, Wilson AC (2014). Cytochrome c551 and the cytochrome c maturation pathway affect virulence gene expression in Bacillus cereus ATCC 14579.
  • Shapyrina EV, Shadrin AM, Solonin AS (2013). [Purification of recombinant Bacillus cereus ResD-ResE proteins expressed in Escherichia coli strains].
  • DOI: 10.1016/j.ijfoodmicro.2015.02.005
    Hayrapetyan H, Muller L, Tempelaars M, Abee T, Nierop Groot M (2015). Comparative analysis of biofilm formation by Bacillus cereus reference strains and undomesticated food isolates and the effect of free iron.
  • DOI: 10.1016/j.ijfoodmicro.2015.02.010
    Warda AK, den Besten HM, Sha N, Abee T, Nierop Groot MN (2015). Influence of food matrix on outgrowth heterogeneity of heat damaged Bacillus cereus spores.
  • DOI: 10.1002/mbo3.239
    Senouci-Rezkallah K, Jobin MP, Schmitt P (2015). Adaptive responses of Bacillus cereus ATCC14579 cells upon exposure to acid conditions involve ATPase activity to maintain their internal pH.
  • DOI: 10.1021/jacs.5b00940
    Wever WJ, Bogart JW, Baccile JA, Chan AN, Schroeder FC, Bowers AA (2015). Chemoenzymatic synthesis of thiazolyl peptide natural products featuring an enzyme-catalyzed formal [4 + 2] cycloaddition.
  • DOI: 10.1016/j.ijfoodmicro.2015.04.043
    Diomande SE, Nguyen-the C, Abee T, Tempelaars MH, Broussolle V, Brillard J (2015). Involvement of the CasK/R two-component system in optimal unsaturation of the Bacillus cereus fatty acids during low-temperature growth.
  • DOI: 10.1371/journal.pone.0133790
    Hwang S, Aronov A, Bar-Peled M (2015). The Biosynthesis of UDP-D-QuiNAc in Bacillus cereus ATCC 14579.
  • DOI: 10.1371/journal.pone.0134872
    Hayrapetyan H, Tempelaars M, Nierop Groot M, Abee T (2015). Bacillus cereus ATCC 14579 RpoN (Sigma 54) Is a Pleiotropic Regulator of Growth, Carbohydrate Metabolism, Motility, Biofilm Formation and Toxin Production.
  • DOI: 10.1016/j.bcp.2015.09.013
    Gwenin VV, Poornima P, Halliwell J, Ball P, Robinson G, Gwenin CD (2015). Identification of novel nitroreductases from Bacillus cereus and their interaction with the CB1954 prodrug.
  • DOI: 10.1128/AEM.02626-15
    Bressuire-Isoard C, Bornard I, Henriques AO, Carlin F, Broussolle V (2015). Sporulation Temperature Reveals a Requirement for CotE in the Assembly of both the Coat and Exosporium Layers of Bacillus cereus Spores.
  • DOI: 10.3389/fmicb.2015.01004
    Omer H, Alpha-Bazin B, Brunet JL, Armengaud J, Duport C (2015). Proteomics identifies Bacillus cereus EntD as a pivotal protein for the production of numerous virulence factors.
  • DOI: 10.3389/fmicb.2015.01063
    Kroeger JK, Hassan K, Voros A, Simm R, Saidijam M, Bettaney KE, Bechthold A, Paulsen IT, Henderson PJ, Kolsto AB (2015). Bacillus cereus e ffl ux protein BC3310 - a multidrug transporter of the unknown major facilitator family, UMF-2.
  • DOI: 10.3109/21691401.2015.1089253
    Wang C, Singh P, Kim YJ, Mathiyalagan R, Myagmarjav D, Wang D, Jin CG, Yang DC (2015). Characterization and antimicrobial application of biosynthesized gold and silver nanoparticles by using Microbacterium resistens.
  • Jitareanu A, Zbancioc AM, Tuchilus C, Balan M, Stanescu U, Tataringa G (2015). alpha,beta-DIBROMOCHALCONE DERIVATIVES--SYNTHESIS AND ANTIMICROBIAL ACTIVITY.
  • DOI: 10.3168/jds.2015-10434
    Jiang M, Zhang F, Wan C, Xiong Y, Shah NP, Wei H, Tao X (2016). Evaluation of probiotic properties of Lactobacillus plantarum WLPL04 isolated from human breast milk.
  • DOI: 10.3168/jds.2015-10587
    Zhang Z, Tao X, Shah NP, Wei H (2016). Antagonistics against pathogenic Bacillus cereus in milk fermentation by Lactobacillus plantarum ZDY2013 and its anti-adhesion effect on Caco-2 cells against pathogens.
  • DOI: 10.1371/journal.pone.0148670
    Warda AK, Tempelaars MH, Boekhorst J, Abee T, Nierop Groot MN (2016). Identification of CdnL, a Putative Transcriptional Regulator Involved in Repair and Outgrowth of Heat-Damaged Bacillus cereus Spores.
  • DOI: 10.1093/femsle/fnw126
    Kovacs AT (2016). The global regulator CodY is required for the fitness of Bacillus cereus in various laboratory media and certain beverages.
  • DOI: 10.1371/journal.pone.0156796
    Warda AK, Siezen RJ, Boekhorst J, Wells-Bennik MH, de Jong A, Kuipers OP, Nierop Groot MN, Abee T (2016). Linking Bacillus cereus Genotypes and Carbohydrate Utilization Capacity.
  • DOI: 10.1016/j.jprot.2016.06.022
    Madeira JP, Omer H, Alpha-Bazin B, Armengaud J, Duport C (2016). Deciphering the interactions between the Bacillus cereus linear plasmid, pBClin15, and its host by high-throughput comparative proteomics.
  • DOI: 10.3389/fmicb.2016.01096
    Warda AK, Tempelaars MH, Abee T, Nierop Groot MN (2016). Recovery of Heat Treated Bacillus cereus Spores Is Affected by Matrix Composition and Factors with Putative Functions in Damage Repair.
  • DOI: 10.1016/j.dib.2016.07.042
    Madeira JP, Alpha-Bazin B, Armengaud J, Omer H, Duport C (2016). Proteome data to explore the impact of pBClin15 on Bacillus cereus ATCC 14579.
  • DOI: 10.1021/jacs.6b05389
    Wever WJ, Bogart JW, Bowers AA (2016). Identification of Pyridine Synthase Recognition Sequences Allows a Modular Solid-Phase Route to Thiopeptide Variants.
  • DOI: 10.1002/cbdv.201600116
    Znati M, Filali I, Jabrane A, Casanova J, Bouajila J, Ben Jannet H (2016). Chemical Composition and In Vitro Evaluation of Antimicrobial, Antioxidant and Antigerminative Properties of the Seed Oil from the Tunisian Endemic Ferula tunetana Pomel ex Batt.
  • DOI: 10.4014/jmb.1604.04094
    Chung HY, Lee KH, Ryu S, Yoon H, Lee JH, Kim HB, Kim H, Jeong HG, Choi SH, Kim BS (2016). Genome Sequence of Bacillus cereus FORC_021, a Food-Borne Pathogen Isolated from a Knife at a Sashimi Restaurant.
  • DOI: 10.1128/AEM.02490-16
    Warda AK, Xiao Y, Boekhorst J, Wells-Bennik MHJ, Nierop Groot MN, Abee T (2017). Analysis of Germination Capacity and Germinant Receptor (Sub)clusters of Genome-Sequenced Bacillus cereus Environmental Isolates and Model Strains.
  • DOI: 10.1074/jbc.M117.777417
    Li Z, Mukherjee T, Bowler K, Namdari S, Snow Z, Prestridge S, Carlton A, Bar-Peled M (2017). A four-gene operon in Bacillus cereus produces two rare spore-decorating sugars.
  • DOI: 10.1016/j.exer.2017.03.007
    Callegan MC, Parkunan SM, Randall CB, Coburn PS, Miller FC, LaGrow AL, Astley RA, Land C, Oh SY, Schneewind O (2017). The role of pili in Bacillus cereus intraocular infection.
  • DOI: 10.1371/journal.pone.0176188
    Hassan KA, Fagerlund A, Elbourne LDH, Voros A, Kroeger JK, Simm R, Tourasse NJ, Finke S, Henderson PJF, Okstad OA, Paulsen IT, Kolsto AB (2017). The putative drug efflux systems of the Bacillus cereus group.
  • DOI: 10.1002/jobm.201700192
    Abeer Mohammed AB, Al-Saman MA, Tayel AA (2017). Antibacterial activity of fusion from biosynthesized acidocin/silver nanoparticles and its application for eggshell decontamination.
  • DOI: 10.1016/j.fm.2017.08.011
    Cetin-Karaca H, Newman MC (2017). Antimicrobial efficacy of phytochemicals against Bacillus cereus in reconstituted infant rice cereal.
  • Foroughifar N, Karimi Beromi S, Pasdar H, Shahi M (2017). Synthesis of Some New Tetrahydropyrimidine Derivatives as Possible Antibacterial Agents.
  • DOI: 10.1371/journal.pone.0184975
    Huillet E, Bridoux L, Wanapaisan P, Rejasse A, Peng Q, Panbangred W, Lereclus D (2017). The CodY-dependent clhAB2 operon is involved in cell shape, chaining and autolysis in Bacillus cereus ATCC 14579.
  • DOI: 10.4315/0362-028X.JFP-17-450
    Hussain MS, Kwon M, Tango CN, Oh DH (2018). Effect of Electrolyzed Water on the Disinfection of Bacillus cereus Biofilms: The Mechanism of Enhanced Resistance of Sessile Cells in the Biofilm Matrix.
  • DOI: 10.1016/j.dib.2018.03.030
    Madeira JP, Alpha-Bazin B, Armengaud J, Duport C (2018). Time-course proteomics dataset to monitor protein-bound methionine oxidation in Bacillus cereus ATCC 14579.
  • DOI: 10.1371/journal.pone.0200958
    Hussain MS, Kwon M, Oh DH (2018). Impact of manganese and heme on biofilm formation of Bacillus cereus food isolates.
  • DOI: 10.1016/j.ijfoodmicro.2018.07.020
    Alvarenga VO, Brancini GTP, Silva EK, da Pia AKR, Campagnollo FB, Braga GUL, Hubinger MD, Sant'Ana AS (2018). Survival variability of 12 strains of Bacillus cereus yielded to spray drying of whole milk.
  • DOI: 10.1089/fpd.2018.2478
    Fernandez YA, Damasceno JL, Abrao F, Silva TS, Candido ALP, Fregonezi NF, Resende FA, Ramos SB, Ambrosio SR, Veneziani RCS, Bastos JK, Martins CHG (2018). Antibacterial, Preservative, and Mutagenic Potential of Copaifera spp. Oleoresins Against Causative Agents of Foodborne Diseases.
  • DOI: 10.1007/s10068-016-0073-z
    Lee JY, Shim JM, Yao Z, Liu X, Lee KW, Kim HJ, Ham KS, Kim JH (2016). Antimicrobial activity of Bacillus amyloliquefaciens EMD17 isolated from Cheonggukjang and potential use as a starter for fermented soy foods.
  • DOI: 10.1007/s10068-016-0234-0
    Lee SK, Lee H (2016). Antimicrobial activity of solvent fractions and bacterial isolates of Korean domestic honey from different floral sources.
  • DOI: 10.1016/j.anaerobe.2018.08.004
    Hong W, Cheng Y, Rao F, Yang J, Cui G, Chen Z, Liao J, Huang X, Zhang J, Wang P, Wang S, Wang Y, Guan Z, Qi X (2018). Co-infection of Clostridioides (Clostridium) difficile GMU1 and Bacillus cereus GMU2 in one patient in Guizhou, China.
  • DOI: 10.1016/j.foodres.2018.08.003
    Hussain MS, Tango CN, Oh DH (2018). Inactivation kinetics of slightly acidic electrolyzed water combined with benzalkonium chloride and mild heat treatment on vegetative cells, spores, and biofilms of Bacillus cereus.
  • DOI: 10.1080/14786419.2019.1569006
    Pasandi Pour A, Farahbakhsh H (2019). Lawsonia inermis L. leaves aqueous extract as a natural antioxidant and antibacterial product.
  • DOI: 10.3389/fmicb.2019.00144
    Carroll LM, Wiedmann M, Mukherjee M, Nicholas DC, Mingle LA, Dumas NB, Cole JA, Kovac J (2019). Characterization of Emetic and Diarrheal Bacillus cereus Strains From a 2016 Foodborne Outbreak Using Whole-Genome Sequencing: Addressing the Microbiological, Epidemiological, and Bioinformatic Challenges.
  • DOI: 10.4315/0362-028X.JFP-18-401
    Jo Y, Bae H, Kim SS, Ban C, Kim SO, Choi YJ (2019). Inactivation of Bacillus cereus ATCC 14579 Spore on Garlic with Combination Treatments of Germinant Compounds and Superheated Steam.
  • DOI: 10.1128/AEM.00486-19
    Francais M, Carlin F, Broussolle V, Nguyen-The C (2019). Bacillus cereus cshA Is Expressed during the Lag Phase of Growth and Serves as a Potential Marker of Early Adaptation to Low Temperature and pH.
  • DOI: 10.4315/0362-028X-58.11.1206
    Pfeifer J, Kessler HG (1995). Heat Resistance of Bacillus cereus Spores Located between Seals and Seal Surfaces.
  • DOI: 10.1016/j.msec.2019.04.041
    Majeed S, Aripin FHB, Shoeb NSB, Danish M, Ibrahim MNM, Hashim R (2019). Bioengineered silver nanoparticles capped with bovine serum albumin and its anticancer and apoptotic activity against breast, bone and intestinal colon cancer cell lines.
  • DOI: 10.1007/s10142-019-00704-0
    Yadav S, Reddy B, Dubey SK (2019). De novo genome assembly and comparative annotation reveals metabolic versatility in cellulolytic bacteria from cropland and forest soils.
  • DOI: 10.6026/97320630015474
    Sridhar J, Gayathri M (2019). Transcriptome based Identification of silver stress responsive sRNAs from Bacillus cereus ATCC14579.
  • DOI: 10.3390/antibiotics8030155
    Swift SM, Etobayeva IV, Reid KP, Waters JJ, Oakley BB, Donovan DM, Nelson DC (2019). Characterization of LysBC17, a Lytic Endopeptidase from Bacillus cereus.
  • DOI: 10.4315/0362-028X.JFP-18-586
    Muhammad AI, Lv R, Liao X, Chen W, Liu D, Ye X, Chen S, Ding T (2019). Modeling the Inactivation of Bacillus cereus in Tiger Nut Milk Treated with Cold Atmospheric Pressure Plasma.
  • DOI: 10.1099/mic.0.000883
    Huillet E, Bridoux L, Barboza I, Lemy C, Andre-Leroux G, Lereclus D (2020). The signaling peptide PapR is required for the activity of the quorum-sensor PlcRa in Bacillus thuringiensis.
  • DOI: 10.3390/microorganisms8060849
    Sindi A, Badsha MB, Nielsen B, Unlu G (2020). Antimicrobial Activity of Six International Artisanal Kefirs Against Bacillus cereus, Listeria monocytogenes, Salmonella enterica serovar Enteritidis, and Staphylococcus aureus.
  • DOI: 10.1186/s12866-020-01893-6
    Ghosh S, Mohapatra B, Satyanarayana T, Sar P (2020). Molecular and taxonomic characterization of arsenic (As) transforming Bacillus sp. strain IIIJ3-1 isolated from As-contaminated groundwater of Brahmaputra river basin, India.
  • DOI: 10.3390/plants9081023
    Thiruvengadam M, Ghimire BK, Kim SH, Yu CY, Oh DH, Chelliah R, Kwon C, Kim YJ, Chung IM (2020). Assessment of Mineral and Phenolic Profiles and Their Association with the Antioxidant, Cytotoxic Effect, and Antimicrobial Potential of Lycium chinense Miller.
  • DOI: 10.1016/j.bbrc.2020.09.048
    Hong J, Park W, Seo H, Kim IK, Kim KJ (2020). Crystal structure of an acetyl-CoA acetyltransferase from PHB producing bacterium Bacillus cereus ATCC 14579.
  • DOI: 10.1016/j.bbrc.2020.09.093
    Seok J, Kim YJ, Kim IK, Kim KJ (2020). Structural basis for stereospecificity to d-amino acid of glycine oxidase from Bacillus cereus ATCC 14579.
  • DOI: 10.1016/j.bbrc.2020.09.136
    Lee SH, Ki D, Kim S, Kim IK, Kim KJ (2020). Biochemical properties and crystal structure of isocitrate lyase from Bacillus cereus ATCC 14579.
  • DOI: 10.1021/acs.jafc.0c06503
    Sagong HY, Kim B, Joo S, Kim KJ (2020). Structural and Functional Characterization of Cystathionine gamma-lyase from Bacillus cereus ATCC 14579.
  • DOI: 10.3390/biology9120456
    Di Cerbo A, Mescola A, Iseppi R, Canton R, Rossi G, Stocchi R, Loschi AR, Alessandrini A, Rea S, Sabia C (2020). Antibacterial Effect of Aluminum Surfaces Untreated and Treated with a Special Anodizing Based on Titanium Oxide Approved for Food Contact.
  • DOI: 10.3390/toxins12120806
    Rudenko N, Nagel A, Zamyatina A, Karatovskaya A, Salyamov V, Andreeva-Kovalevskaya Z, Siunov A, Kolesnikov A, Shepelyakovskaya A, Boziev K, Melnik B, Brovko F, Solonin A (2020). A Monoclonal Antibody against the C-Terminal Domain of Bacillus cereus Hemolysin II Inhibits HlyII Cytolytic Activity.
  • DOI: 10.1016/j.ijbiomac.2020.12.174
    Park J, Kim YJ, Lee D, Kim KJ (2020). Structural basis for nucleotide-independent regulation of acyl-CoA thioesterase from Bacillus cereus ATCC 14579.
  • DOI: 10.3390/microorganisms9020248
    Di Cerbo A, Mescola A, Rosace G, Stocchi R, Rossi G, Alessandrini A, Preziuso S, Scarano A, Rea S, Loschi AR, Sabia C (2021). Antibacterial Effect of Stainless Steel Surfaces Treated with a Nanotechnological Coating Approved for Food Contact.
  • DOI: 10.1016/j.ijfoodmicro.2021.109285
    Cayemitte PE, Gerliani N, Raymond P, Aider M (2021). Study of the impacts of electro-activated solutions of calcium lactate, calcium ascorbate and their equimolar mixture combined with moderate heat treatments on the spores of Bacillus cereus ATCC 14579 under model conditions and in fresh salmon.
  • DOI: 10.1111/lam.13527
    Yang Y, Foster JT, Yi M, Zhan L, Zhang Y, Zhou B, Jiang J, Mei L (2021). Phenotypic homogeneity of emetic Bacillus cereus isolates in China.
  • DOI: 10.1186/s12864-021-07962-y
    Hamitouche F, Gaillard JC, Schmitt P, Armengaud J, Duport C, Dedieu L (2021). Redox proteomic study of Bacillus cereus thiol proteome during fermentative anaerobic growth.
  • DOI: 10.1016/j.envpol.2021.118343
    Saeed M, Ilyas N, Bibi F, Jayachandran K, Dattamudi S, Elgorban AM (2021). Biodegradation of PAHs by Bacillus marsiflavi, genome analysis and its plant growth promoting potential.
  • DOI: 10.1016/j.bbrc.2021.10.051
    Seok J, Hong J, Park J, Kim KJ (2021). Structural analysis of the peptidoglycan editing factor PdeF from Bacillus cereus ATCC 14579.
  • DOI: 10.3390/biology11010097
    Di Cerbo A, Mescola A, Rosace G, Trovato V, Canton R, Iseppi R, Stocchi R, Ghazanfar S, Rea S, Loschi AR, Sabia C (2022). A Time-Course Study on a Food Contact Material (FCM)-Certified Coating Based on Titanium Oxide Deposited onto Aluminum.
  • DOI: 10.1021/acsomega.1c06124
    Cayemitte PE, Gerliani N, Raymond P, Aider M (2022). Study of the Antibacterial Potency of Electroactivated Solutions of Calcium Lactate and Calcium Ascorbate on Bacillus cereus ATCC 14579 Vegetative Cells.
  • DOI: 10.3390/md20020128
    Dzeha T, Hall MJ, Burgess JG (2022). Micrococcin P1 and P2 from Epibiotic Bacteria Associated with Isolates of Moorea producens from Kenya.
  • DOI: 10.1128/mra.01106-21
    Matsunaka M, Thanh NC, Uedoi T, Iida T, Fujino Y, Ohmori T, Hiromasa Y, Ohshima T, Doi K (2022). Complete Genome Sequence of Bacillus cereus Strain HT18, Isolated from Forest Soil.
  • DOI: 10.1107/S2059798322002674
    Park J, Hong J, Seok J, Hong H, Seo H, Kim KJ (2022). Structural studies of a novel auxiliary-domain-containing phenylalanine hydroxylase from Bacillus cereus ATCC 14579.
  • DOI: 10.1055/a-1891-1119
    Karadag AE, Caskurlu A, Demirci B, Demirci F (2022). Binary Synergistic Combinations of Lavender and Fennel Essential Oils with Amoxicillin.
  • DOI: 10.3390/microorganisms10091774
    Wang Y, Setlow P, Brul S (2022). Genomic versus Plasmid-Borne Expression of Germinant Receptor Proteins in Bacillus cereus Strain 14579.
  • DOI: 10.4265/bio.27.143
    Kuwana R, Yamazawa R, Ito K, Takamatsu H (2022). The Study of Diversity in Sporulation among Closely Genetically Related Bacillus cereus Strains.
  • DOI: 10.1016/j.heliyon.2022.e11693
    Almohammadi AR, Abdel-Shafi S, Tartour E, Enan G (2022). Inhibitory action of three lactic acid bacteria cultures on some food-borne pathogens during pickling of green olive fruits.
  • DOI: 10.1016/j.resmic.2023.104030
    Vittoria M, Saggese A, Di Gregorio Barletta G, Castaldi S, Isticato R, Baccigalupi L, Ricca E (2023). Sporulation efficiency and spore quality in a human intestinal isolate of Bacillus cereus.
  • DOI: 10.1186/s12866-023-02783-3
    Yeak KYC, Tempelaars M, Wu JL, Westerveld W, Reder A, Michalik S, Dhople VM, Volker U, Pane-Farre J, Wells-Bennik MHJ, Abee T (2023). SigB modulates expression of novel SigB regulon members via Bc1009 in non-stressed and heat-stressed cells revealing its alternative roles in Bacillus cereus.
  • DOI: 10.1016/j.resmic.2023.104072
    Huijboom L, Tempelaars M, Fan M, Zhu Y, Boeren S, van der Linden E, Abee T (2023). l-tyrosine modulates biofilm formation of Bacillus cereus ATCC 14579.
  • DOI: 10.3389/fmicb.2023.1113642
    Taylor-Joyce G, Manoharan S, Brooker TA, Hernandez-Rodriguez CS, Baillie L, Oyston PCF, Hapeshi A, Waterfield NR (2023). The influence of extrachromosomal elements in the anthrax "cross-over" strain Bacillus cereus G9241.
  • DOI: 10.1039/d3ra00802a
    Xu N, Du LH, Chen YC, Zhang JH, Zhu QF, Chen R, Peng GP, Wang QM, Yu HZ, Rao LQ (2023). Lonicera japonica Thunb. as a promising antibacterial agent for Bacillus cereus ATCC14579 based on network pharmacology, metabolomics, and in vitro experiments.
  • DOI: 10.3390/microorganisms11071826
    Calvigioni M, Panattoni A, Biagini F, Donati L, Mazzantini D, Massimino M, Daddi C, Celandroni F, Vozzi G, Ghelardi E (2023). Impact of Bacillus cereus on the Human Gut Microbiota in a 3D In Vitro Model.
  • DOI: 10.5808/gi.23030
    Sornchuer P, Saninjuk K, Tingpej P (2023). Whole genome sequence analyses of thermotolerant Bacillus sp. isolates from food.
  • DOI: 10.3389/fmicb.2023.1295262
    Muller S, DeLeon O, Atkinson SN, Saravia F, Kellogg S, Shank EA, Kirby JR (2023). Thiocillin contributes to the ecological fitness of Bacillus cereus ATCC 14579 during interspecies interactions with Myxococcus xanthus.
  • DOI: 10.3389/fcimb.2023.1304677
    Coburn PS, Miller FC, LaGrow AL, Mursalin H, Gregory A, Parrott A, Astley D, Callegan MC (2023). Virulence-related genotypic differences among Bacillus cereus ocular and gastrointestinal isolates and the relationship to endophthalmitis pathogenesis.
  • DOI: 10.3390/antibiotics12121677
    Monteiro EDS, da Silva FS, Gomes KO, do Prado BA, Dos Santos RD, Gomes da Camara CA, de Moraes MM, Silva ICRD, de Macedo VT, Gelfuso GM, Sa Barreto LCL, Orsi DC (2023). Characterization and Determination of the Antibacterial Activity of Baccharis dracunculifolia Essential-Oil Nanoemulsions.
  • DOI: 10.1016/j.ijfoodmicro.2024.110617
    Li Y, Luo L, Wang W, Hong B, Ma Y, Wang J (2024). Characterization of a cell wall hydrolase with high activity against vegetative cells, spores and biofilm of Bacillus cereus.
  • DOI: 10.1016/j.biochi.2024.02.008
    Duport C, Armengaud J, Schmitt C, Morin D, Lacapere JJ (2024). Elucidating the pivotal role of TSPO in porphyrin-related cellular processes, in Bacillus cereus.
  • DOI: 10.1039/d4ra90032d
    Xu N, Du LH, Chen YC, Zhang JH, Zhu QF, Chen R, Peng GP, Wang QM, Yu HZ, Rao LQ (2024). Correction: Lonicera japonica Thunb. as a promising antibacterial agent for Bacillus cereus ATCC14579 based on network pharmacology, metabolomics, and in vitro experiments.
  • DOI: 10.1021/acsami.4c02355
    Manceau M, Farre C, Lagarde F, Mathey R, Buhot A, Vidic J, Leguillier V, Hou Y, Chaix C (2024). Investigation of the Affinity of Aptamers for Bacteria by Surface Plasmon Resonance Imaging Using Nanosomes.
  • DOI: 10.1111/mmi.15299
    Mazzantini D, Gherardini G, Rossi V, Celandroni F, Calvigioni M, Panattoni A, Massimino M, Lupetti A, Ghelardi E (2024). Dissecting the role of the MS-ring protein FliF in Bacillus cereus flagella-related functions.
  • DOI: 10.1016/j.fm.2008.06.001
    Landete JM, Arena ME, Pardo I, Manca de Nadra MC, Ferrer S (2008). Comparative survey of putrescine production from agmatine deamination in different bacteria.
  • DOI: 10.1016/j.ijfoodmicro.2009.07.013
    Martinez-Blanch JF, Sanchez G, Garay E, Aznar R (2009). Development of a real-time PCR assay for detection and quantification of enterotoxigenic members of Bacillus cereus group in food samples.
  • DOI: 10.4315/0362-028x-73.8.1480
    Martinez-Blanch JF, Sanchez G, Garay E, Aznar R (2010). Evaluation of a real-time PCR assay for the detection and quantification of Bacillus cereus group spores in food.
  • DOI: 10.1111/j.1574-6968.2011.02254.x
    Triado-Margarit X, Vila X, Galinski EA (2011). Osmoadaptative accumulation of Nvarepsilon-acetyl-beta-lysine in green sulfur bacteria and Bacillus cereus CECT 148T.
  • DOI: 10.1128/JB.01265-13
    Schurmann M, Demming RM, Krewing M, Rose J, Wubbeler JH, Steinbuchel A (2013). Identification of 3-sulfinopropionyl coenzyme A (CoA) desulfinases within the Acyl-CoA dehydrogenase superfamily.
  • DOI: 10.1099/00221287-139-4-775
    Jahns T, Kaltwasser H (1993). Properties of the cold-labile NAD(+)-specific glutamate dehydrogenase from Bacillus cereus DSM 31.
  • DOI: 10.1016/j.jpba.2018.06.055
    Fumagalli L, Regazzoni LG, Straniero V, Valoti E, Aldini G, Vistoli G, Carini M, Picozzi C (2018). Stressed degradation studies of domiphen bromide by LC-ESI-MS/MS identify a novel promising antimicrobial agent.
  • DOI: 10.3390/microorganisms8121895
    Fraberger V, Ammer C, Domig KJ (2020). Functional Properties and Sustainability Improvement of Sourdough Bread by Lactic Acid Bacteria.
  • DOI: 10.1038/s41598-024-66700-y
    Abdel-Nasser A, Badr AN, Fathy HM, Ghareeb MA, Barakat OS, Hathout AS (2024). Antifungal, antiaflatoxigenic, and cytotoxic properties of bioactive secondary metabolites derived from Bacillus species.
  • DOI: 10.1128/AEM.65.4.1483-1490.1999
    Yamada S, Ohashi E, Agata N, Venkateswaran K (1999). Cloning and nucleotide sequence analysis of gyrB of Bacillus cereus, B. thuringiensis, B. mycoides, and B. anthracis and their application to the detection of B. cereus in rice.
  • DOI: 10.1271/bbb.64.1210
    Kim SI, Miyamoto T, Honjoh KI, Hio M, Hatano S (2000). Molecular cloning, overproduction and characterization of the Bacillus cereus IMP dehydrogenase.
  • DOI: 10.1016/0022-2011(90)90078-k
    Rahmet-Alla M, Rowley AF (1990). Studies on the cellular defense reactions of the madeira cockroach, Leucophaea maderae: in vitro phagocytosis of different strains of Bacillus cereus and their effect on hemocyte viability.
  • DOI: 10.1111/j.1365-2672.1990.tb01548.x
    Husmark U, Ronner U (1990). Forces involved in adhesion of Bacillus cereus spores to solid surfaces under different environmental conditions.
  • DOI: 10.1016/s0309-1740(99)00129-1
    Con AH, Gokalp HY (2000). Production of bacteriocin-like metabolites by lactic acid cultures isolated from sucuk samples.
  • DOI: 10.1007/BF02975108
    Kaplancikli ZA, Turan-Zitouni G, Revial G, Guven K (2004). Synthesis and study of antibacterial and antifungal activities of novel 2-[[(benzoxazole/benzimidazole-2-yl)sulfanyl] acetylamino]thiazoles.
  • DOI: 10.1016/j.ejmech.2006.10.001
    Ozdemir A, Turan-Zitouni G, Kaplancikli ZA, Revial G, Guven K (2006). Synthesis and antimicrobial activity of 1-(4-aryl-2-thiazolyl)-3-(2-thienyl)-5-aryl-2-pyrazoline derivatives.
  • DOI: 10.1016/j.ejmech.2007.03.019
    Kaplancikli ZA, Turan-Zitouni G, Ozdemir A, Revial G (2007). New triazole and triazolothiadiazine derivatives as possible antimicrobial agents.
  • DOI: 10.1089/jmf.2011.0315
    Herken EN, Celik A, Aslan M, Aydinlik N (2012). The constituents of essential oil: antimicrobial and antioxidant activity of Micromeria congesta Boiss. & Hausskn. ex Boiss. from East Anatolia.
  • DOI: 10.1128/AEM.00312-11
    Soriano-Maldonado P, Martinez-Gomez AI, Andujar-Sanchez M, Neira JL, Clemente-Jimenez JM, Las Heras-Vazquez FJ, Rodriguez-Vico F, Martinez-Rodriguez S (2011). Biochemical and mutational studies of the Bacillus cereus CECT 5050T formamidase support the existence of a C-E-E-K tetrad in several members of the nitrilase superfamily.
  • DOI: 10.1099/jmm.0.47642-0
    Kim W, Kim JY, Cho SL, Nam SW, Shin JW, Kim YS, Shin HS (2008). Glycosyltransferase: a specific marker for the discrimination of Bacillus anthracis from the Bacillus cereus group.
  • DOI: 10.3390/plants12040797
    Yeo HJ, Kwon MJ, Han SY, Jeong JC, Kim CY, Park SU, Park CH (2023). Effects of Carbohydrates on Rosmarinic Acid Production and In Vitro Antimicrobial Activities in Hairy Root Cultures of Agastache rugosa.
  • DOI: 10.1016/j.foodres.2023.113619
    Yeo HJ, Ki WY, Lee S, Kim CY, Kim JK, Park SU, Park CH (2023). Metabolite profiles and biological activities of different phenotypes of Chinese cabbage (Brassica rapa ssp. Pekinensis).
  • DOI: 10.4315/0362-028x-69.9.2168
    Tsai GJ, Tsai MT, Lee JM, Zhong MZ (2006). Effects of chitosan and a low-molecular-weight chitosan on Bacillus cereus and application in the preservation of cooked rice.
  • DOI: 10.1021/jf902611h
    Chen GH, Chen WM, Huang GT, Chen YW, Jiang ST (2009). Expression of recombinant antibacterial lactoferricin-related peptides from Pichia pastoris expression system.
Outside links and data sources
Retrieved 23 days ago via StrainInfo API (CC BY 4.0)

Metadata

Cannonical URL
https://seqco.de/s:19926
Local history
  • Registered 8 months ago
  • Last modified 23 days ago
© 2022-2025 The SeqCode Initiative
  All information contributed to the SeqCode Registry is released under the terms of the Creative Commons Attribution (CC BY) 4.0 license