Strain sc|0020790


This strain is associated as type material for multiple names:

StrainInfo: SI-ID 92102 T

Taxon
Alcaligenes faecalisT
Cultures (45)
LMG 1229 = ATCC 8750 = CCM 1052 = CCUG 1325 = CCUG 1814 = DSM 30030 = IAM 12586 = IFO 13111 = IMET 10443 = JCM 1474 = LMG 2100 = LMG 3366 = LMG 3369 = LMG 3371 = NCDO 868 = NCIB 8156 = NCTC 11953 = NBIMCC 153 = NCIMB 8156 = IAM12369 = VKM B-1518 = CIP 60.80 = CECT 928 = CCRC 10828 = NCAIM B.01104 = NCFB 868 = VTT E-76056 = KCTC 2678 = AS 1.1786 = NBRC 13111 = CIP 55.84 = HAMBI 1907 = BCRC 10828 = CCT 0192 = CCT 1434 = NCAIM B.02076 = NCIM 2262 = NCIM 2105 = CNCTC 5644 = JCM 20522 = JCM 20663 = CGMCC 1.2006 = CGMCC 1.1786 = CGMCC 1.0924 = VTT E-97056
Other Designations (25)
USCC 2593 = CCTM 2801 = Conn 16 = FIRDI 828 = USCC 1366 = Hugh 135 = Lautrop AB60 = USCC 2062 = IAW 153 = Hugh R 135 = PCM 2223 = H.J. Conn 16 = Conn H.J. 16 = DSMZ 30030 = CIP 60-80 = LMG 1229T QC 10/01 = 16 = CCTM La 2801 = 31882 = LMAU A13 = NCIB 8156. NCDO 868 = NICB 8156 = RH 135 = 16 (R = 135
Sequences (30)
Associated Publications (16)
  • DOI: 10.2323/jgam.59.089
    Yokoyama S, Adachi Y, Asakura S, Kohyama E (2013). Characterization of Alcaligenes faecalis strain AD15 indicating biocontrol activity against plant pathogens.
  • DOI: 10.1099/ijs.0.64126-0
    Wubbeler JH, Lutke-Eversloh T, Van Trappen S, Vandamme P, Steinbuchel A (2006). Tetrathiobacter mimigardefordensis sp. nov., isolated from compost, a betaproteobacterium capable of utilizing the organic disulfide 3,3'-dithiodipropionic acid.
  • DOI: 10.1016/0003-9861(85)90654-x
    Lewis MA, Timkovich R, Cotton TM (1985). A comparative study of the resonance Raman spectra of bacterial cytochromes.
  • DOI: 10.1093/protein/gzm032
    Kiziak C, Klein J, Stolz A (2007). Influence of different carboxy-terminal mutations on the substrate-, reaction- and enantiospecificity of the arylacetonitrilase from Pseudomonas fluorescens EBC191.
  • DOI: 10.1128/AEM.00301-09
    Kiziak C, Stolz A (2009). Identification of amino acid residues responsible for the enantioselectivity and amide formation capacity of the Arylacetonitrilase from Pseudomonas fluorescens EBC191.
  • DOI: 10.1128/aem.57.10.3028-3032.1991
    Yamamoto K, Oishi K, Fujimatsu I, Komatsu K (1991). Production of R-(-)-mandelic acid from mandelonitrile by Alcaligenes faecalis ATCC 8750.
  • DOI: 10.1016/0378-1097(90)90278-x
    Castignetti D, Palutsis D, Turley J (1990). An examination of proton translocation and energy conservation during heterotrophic nitrification.
  • DOI: 10.1016/0162-0134(84)85060-6
    Timkovich R, Cork MS, Taylor PV (1984). Proton NMR spectroscopy of Alcaligenes cytochrome c556.
  • DOI: 10.1021/bi00300a010
    Timkovich R, Cork MS (1984). Proton NMR spectroscopy of cytochrome c-554 from Alcaligenes faecalis.
  • DOI: 10.1021/jf048827q
    Rey P, Rossi JC, Taillades J, Gros G, Nore O (2004). Hydrolysis of nitriles using an immobilized nitrilase: applications to the synthesis of methionine hydroxy analogue derivatives.
  • DOI: 10.1021/ja503123m
    Chen Z, Zhou L, Bing W, Zhang Z, Li Z, Ren J, Qu X (2014). Light controlled reversible inversion of nanophosphor-stabilized Pickering emulsions for biphasic enantioselective biocatalysis.
  • DOI: 10.3390/ijms21217859
    Kim JS, Patel SKS, Tiwari MK, Lai C, Kumar A, Kim YS, Kalia VC, Lee JK (2020). Phe-140 Determines the Catalytic Efficiency of Arylacetonitrilase from Alcaligenes faecalis.
  • DOI: 10.1128/aem.55.8.2068-2072.1989
    Papen H, von Berg R, Hinkel I, Thoene B, Rennenberg H (1989). Heterotrophic nitrification by Alcaligenes faecalis: NO2-, NO3-, N2O, and NO production in exponentially growing cultures.
  • DOI: 10.1271/bbb.64.569
    Hatakeyama K, Goto M, Uchida Y, Kobayashi M, Terasawa M, Yukawa H (2000). Molecular analysis of maleate cis-trans isomerase from thermophilic bacteria.
  • DOI: 10.1006/bbrc.1997.7430
    Hatakeyama K, Asai Y, Uchida Y, Kobayashi M, Terasawa M, Yukawa H (1997). Gene cloning and characterization of maleate cis-trans isomerase from Alcaligenes faecalis.
  • DOI: 10.1007/s00253-015-6812-x
    Nojiri M, Hibi M, Shizawa H, Horinouchi N, Yasohara Y, Takahashi S, Ogawa J (2015). Imidase catalyzing desymmetric imide hydrolysis forming optically active 3-substituted glutaric acid monoamides for the synthesis of gamma-aminobutyric acid (GABA) analogs.
Outside links and data sources
Retrieved about 1 month ago via StrainInfo API (CC BY 4.0)

Metadata

Cannonical URL
https://seqco.de/s:20790
Local history
  • Registered 8 months ago
  • Last modified about 1 month ago
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