-
DOI: 10.1016/0378-1097(92)90476-5
Hustede E, Steinbuchel A, Schlegel HG
(1992).
Cloning of poly(3-hydroxybutyric acid) synthase genes of Rhodobacter sphaeroides and Rhodospirillum rubrum and heterologous expression in Alcaligenes eutrophus.
-
DOI: 10.1111/j.1574-695X.1994.tb00499.x
Kirikae T, Schade FU, Kirikae F, Qureshi N, Takayama K, Rietschel ET
(1994).
Diphosphoryl lipid A derived from the lipopolysaccharide (LPS) of Rhodobacter sphaeroides ATCC 17023 is a potent competitive LPS inhibitor in murine macrophage-like J774.1 cells.
-
DOI: 10.1006/jmbi.1993.1246
Buchanan SK, Fritzsch G, Ermler U, Michel H
(1993).
New crystal form of the photosynthetic reaction centre from Rhodobacter sphaeroides of improved diffraction quality.
-
DOI: 10.1371/journal.pone.0086830
Erbakan M, Shen YX, Grzelakowski M, Butler PJ, Kumar M, Curtis WR
(2014).
Molecular cloning, overexpression and characterization of a novel water channel protein from Rhodobacter sphaeroides.
-
DOI: 10.1007/s12010-016-2005-z
Liu S, Zhang G, Li J, Li X, Zhang J
(2016).
Optimization of Biomass and 5-Aminolevulinic Acid Production by Rhodobacter sphaeroides ATCC17023 via Response Surface Methodology.
-
DOI: 10.1186/s12934-021-01695-z
Yang Y, Li L, Sun H, Li Z, Qi Z, Liu X
(2021).
Improving CoQ(10) productivity by strengthening glucose transmembrane of Rhodobacter sphaeroides.
-
DOI: 10.1007/s002030050321
Sturgis JN, Niedermann RA
(1996).
The effect of different levels of the B800-850 light-harvesting complex on intracytoplasmic membrane development in Rhodobacter sphaeroides.
-
DOI: 10.1111/j.1432-1033.1997.t01-1-00564.x
Babic S, Hunter CN, Rakhlin NJ, Simons RW, Phillips-Jones MK
(1997).
Molecular characterisation of the pifC gene encoding translation initiation factor 3, which is required for normal photosynthetic complex formation in Rhodobacter sphaeroides NCIB 8253.
-
DOI: 10.1016/j.febslet.2006.04.079
Potter CA, Jeong EL, Williamson MP, Henderson PJ, Phillips-Jones MK
(2006).
Redox-responsive in vitro modulation of the signalling state of the isolated PrrB sensor kinase of Rhodobacter sphaeroides NCIB 8253.
-
DOI: 10.3923/pjbs.2009.1462.1467
Alalayah WM, Kalil MS, Kadhum AA, Jahim JM, Jaapar SZ, Alauj NM
(2009).
Bio-hydrogen production using a two-stage fermentation process.
-
DOI: 10.3923/pjbs.2009.1253.1259
Jaapar SZ, Kalil MS, Anuar N
(2009).
The effect of aeration, agitation and light on biohydrogen production by Rhodobacter sphaeroides NCIMB 8253.
-
DOI: 10.3390/microorganisms10112197
Iwai R, Uchida S, Yamaguchi S, Sonoda F, Tsunoda K, Nagata H, Nagata D, Koga A, Goto M, Maki TA, Hayashi S, Yamamoto S, Miyasaka H
(2022).
Effects of Seed Bio-Priming by Purple Non-Sulfur Bacteria (PNSB) on the Root Development of Rice.
-
DOI: 10.3390/microorganisms11071676
Iwai R, Uchida S, Yamaguchi S, Nagata D, Koga A, Hayashi S, Yamamoto S, Miyasaka H
(2023).
Effects of LPS from Rhodobacter sphaeroides, a Purple Non-Sulfur Bacterium (PNSB), on the Gene Expression of Rice Root.
-
DOI: 10.1042/bj3310897
Reyes F, Gavira M, Castillo F, Moreno-Vivian C
(1998).
Periplasmic nitrate-reducing system of the phototrophic bacterium Rhodobacter sphaeroides DSM 158: transcriptional and mutational analysis of the napKEFDABC gene cluster.
-
DOI: 10.1074/jbc.M406502200
Olmo-Mira MF, Gavira M, Richardson DJ, Castillo F, Moreno-Vivian C, Roldan MD
(2004).
NapF is a cytoplasmic iron-sulfur protein required for Fe-S cluster assembly in the periplasmic nitrate reductase.
-
DOI: 10.1111/j.1365-2958.1996.tb02475.x
Reyes F, Roldan MD, Klipp W, Castillo F, Moreno-Vivian C
(1996).
Isolation of periplasmic nitrate reductase genes from Rhodobacter sphaeroides DSM 158: structural and functional differences among prokaryotic nitrate reductases.
-
DOI: 10.1128/JB.184.6.1693-1702.2002
Gavira M, Roldan MD, Castillo F, Moreno-Vivian C
(2002).
Regulation of nap gene expression and periplasmic nitrate reductase activity in the phototrophic bacterium Rhodobacter sphaeroides DSM158.
-
DOI: 10.1099/ijs.0.65642-0
Arunasri K, Venkata Ramana V, Sproer C, Sasikala Ch, Ramana ChV
(2008).
Rhodobacter megalophilus sp. nov., a phototroph from the Indian Himalayas possessing a wide temperature range for growth.
-
DOI: 10.1099/ijs.0.011718-0
Girija KR, Sasikala C, Ramana CV, Sproer C, Takaichi S, Thiel V, Imhoff JF
(2009).
Rhodobacter johrii sp. nov., an endospore-producing cryptic species isolated from semi-arid tropical soils.
-
DOI: 10.1016/j.biortech.2014.10.061
Krujatz F, Hartel P, Helbig K, Haufe N, Thierfelder S, Bley T, Weber J
(2014).
Hydrogen production by Rhodobacter sphaeroides DSM 158 under intense irradiation.
-
DOI: 10.1002/bit.25667
Krujatz F, Illing R, Krautwer T, Liao J, Helbig K, Goy K, Opitz J, Cuniberti G, Bley T, Weber J
(2015).
Light-field-characterization in a continuous hydrogen-producing photobioreactor by optical simulation and computational fluid dynamics.