ライフサイエンスコーパス: C. acetobutylicum

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1 n of the TCA cycle and central metabolism of C. acetobutylicum.

2 aracterization of Rex-mediated regulation in C. acetobutylicum.

3 nd the highest (ca. 200 mM) ever reported in C. acetobutylicum.

4 formation and oxidative stress tolerance in C. acetobutylicum.

5 itch from acidogenesis to solventogenesis in C. acetobutylicum.

6 Importantly, analysis of the proteome of C. acetobutylicum 824 by electrospray ionization-mass sp

7 ose and related O-alpha-linked glucosides by C. acetobutylicum 824.

8 In vitro gel retardation experiments using C. acetobutylicum adc and C. beijerinckii ptb promoter f

9 First, we generated three strains, C. acetobutylicum ATCC 824 (pADC38AS), 824(pADC68AS), an

10 sfully reproduce ABE fermentations of the WT C. acetobutylicum (ATCC 824), as well as its mutants, us

11 nes into a clostridial chromosome--here, the C. acetobutylicum chromosome--with the aim of altering c

12 ntogenesis pathway and of the cellulosome of C. acetobutylicum comprise a new set of metabolic capaci

13 hemical and genetic approaches, we show that C. acetobutylicum forms Asn and Asn-tRNA(Asn) by tRNA-de

14 However, the C. acetobutylicum genome also contains a significant num

15 C. acetobutylicum grows on a variety of alpha-linked glu

16 In C. acetobutylicum harboring the subclone, the activities

17 our cloning context) into the chromosome of C. acetobutylicum in three steps.

18 uggest an autostimulatory role for sigmaF in C. acetobutylicum, in contrast to the model organism for

19 ed that the five orphan histidine kinases of C. acetobutylicum interact directly with Spo0A to contro

20 Extractive fermentation of C. acetobutylicum is operated in fed-batch mode with a c

21 Coexpression of the C. acetobutylicum maturation proteins with various algal

22 st PHX genes in all these genomes except for C. acetobutylicum (not PHX), and B. subtilis, and B. hal

23 When a C. acetobutylicum pSOL1 megaplasmid-deficient strain M5

24 Novel members of the C. acetobutylicum Rex regulon were identified and experi

25 peron was subcloned into an Escherichia coli-C. acetobutylicum shuttle vector.

26 The C. acetobutylicum sigK deletion (DeltasigK) mutant was u

27 lases from Bacillus, Erwinia carotovora, and C. acetobutylicum species.

28 lysis of 824(pMSPOA) (a spo0A-overexpressing C. acetobutylicum strain with enhanced sporulation) agai

29 Comparison of C. acetobutylicum to Bacillus subtilis reveals significa

30 Inactivation of solR in C. acetobutylicum via homologous recombination yielded m

31 Here the sigF gene in C. acetobutylicum was successfully disrupted and silence

32 nes identified in B. subtilis are missing in C. acetobutylicum, which suggests major differences in t

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