Martin-Verstraete I - Search Results

1

From ubiquity to specificity: The diverse functions of bacterial thioredoxin systems.

Anjou C, Lotoux A, Morvan C, Martin-Verstraete I. Anjou C, et al. Among authors: martin verstraete i. Environ Microbiol. 2024 Jun;26(6):e16668. doi: 10.1111/1462-2920.16668. Environ Microbiol. 2024. PMID: 38899743 Review.

2

The Bacillus subtilis crh gene encodes a HPr-like protein involved in carbon catabolite repression.

Galinier A, Haiech J, Kilhoffer MC, Jaquinod M, Stülke J, Deutscher J, Martin-Verstraete I. Galinier A, et al. Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8439-44. doi: 10.1073/pnas.94.16.8439. Proc Natl Acad Sci U S A. 1997. PMID: 9237995 Free PMC article.

3

Levanase operon of Bacillus subtilis includes a fructose-specific phosphotransferase system regulating the expression of the operon.

Martin-Verstraete I, Débarbouillé M, Klier A, Rapoport G. Martin-Verstraete I, et al. J Mol Biol. 1990 Aug 5;214(3):657-71. doi: 10.1016/0022-2836(90)90284-S. J Mol Biol. 1990. PMID: 2117666

4

The catabolite control protein CcpA controls ammonium assimilation in Bacillus subtilis.

Faires N, Tobisch S, Bachem S, Martin-Verstraete I, Hecker M, Stülke J. Faires N, et al. J Mol Microbiol Biotechnol. 1999 Aug;1(1):141-8. J Mol Microbiol Biotechnol. 1999. PMID: 10941796

5

Control of methionine synthesis and uptake by MetR and homocysteine in Streptococcus mutans.

Sperandio B, Gautier C, McGovern S, Ehrlich DS, Renault P, Martin-Verstraete I, Guédon E. Sperandio B, et al. J Bacteriol. 2007 Oct;189(19):7032-44. doi: 10.1128/JB.00703-07. Epub 2007 Aug 3. J Bacteriol. 2007. PMID: 17675375 Free PMC article.

6

Regulation of the Bacillus subtilis ytmI operon, involved in sulfur metabolism.

Burguière P, Fert J, Guillouard I, Auger S, Danchin A, Martin-Verstraete I. Burguière P, et al. J Bacteriol. 2005 Sep;187(17):6019-30. doi: 10.1128/JB.187.17.6019-6030.2005. J Bacteriol. 2005. PMID: 16109943 Free PMC article.

7

The transcriptional regulator LevR of Bacillus subtilis has domains homologous to both sigma 54- and phosphotransferase system-dependent regulators.

Débarbouillé M, Martin-Verstraete I, Klier A, Rapoport G. Débarbouillé M, et al. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2212-6. doi: 10.1073/pnas.88.6.2212. Proc Natl Acad Sci U S A. 1991. PMID: 1900939 Free PMC article.

8

The alternative sigma factor σ^B plays a crucial role in adaptive strategies of Clostridium difficile during gut infection.

Kint N, Janoir C, Monot M, Hoys S, Soutourina O, Dupuy B, Martin-Verstraete I. Kint N, et al. Environ Microbiol. 2017 May;19(5):1933-1958. doi: 10.1111/1462-2920.13696. Epub 2017 Mar 21. Environ Microbiol. 2017. PMID: 28198085

9

CotL, a new morphogenetic spore coat protein of Clostridium difficile.

Alves Feliciano C, Douché T, Giai Gianetto Q, Matondo M, Martin-Verstraete I, Dupuy B. Alves Feliciano C, et al. Environ Microbiol. 2019 Mar;21(3):984-1003. doi: 10.1111/1462-2920.14505. Epub 2019 Feb 21. Environ Microbiol. 2019. PMID: 30556639

10

The σ^B signalling activation pathway in the enteropathogen Clostridioides difficile.

Kint N, Alves Feliciano C, Hamiot A, Denic M, Dupuy B, Martin-Verstraete I. Kint N, et al. Environ Microbiol. 2019 Aug;21(8):2852-2870. doi: 10.1111/1462-2920.14642. Epub 2019 May 15. Environ Microbiol. 2019. PMID: 31032549

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