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1 imary metabolism and metabolic regulation of C. acetobutylicum.
2 n of the TCA cycle and central metabolism of C. acetobutylicum.
3 nd the highest (ca. 200 mM) ever reported in C. acetobutylicum.
4 aracterization of Rex-mediated regulation in C. acetobutylicum.
5  formation and oxidative stress tolerance in C. acetobutylicum.
6 itch from acidogenesis to solventogenesis in C. acetobutylicum.
7     Importantly, analysis of the proteome of C. acetobutylicum 824 by electrospray ionization-mass sp
8 ose and related O-alpha-linked glucosides by C. acetobutylicum 824.
9   In vitro gel retardation experiments using C. acetobutylicum adc and C. beijerinckii ptb promoter f
10           First, we generated three strains, C. acetobutylicum ATCC 824 (pADC38AS), 824(pADC68AS), an
11 sfully reproduce ABE fermentations of the WT C. acetobutylicum (ATCC 824), as well as its mutants, us
12 nes into a clostridial chromosome--here, the C. acetobutylicum chromosome--with the aim of altering c
13 ntogenesis pathway and of the cellulosome of C. acetobutylicum comprise a new set of metabolic capaci
14  RNA becomes the fourth most abundant RNA in C. acetobutylicum, excluding ribosomal RNAs and transfer
15 hemical and genetic approaches, we show that C. acetobutylicum forms Asn and Asn-tRNA(Asn) by tRNA-de
16                                 However, the C. acetobutylicum genome also contains a significant num
17                                              C. acetobutylicum grows on a variety of alpha-linked glu
18                                           In C. acetobutylicum harboring the subclone, the activities
19  our cloning context) into the chromosome of C. acetobutylicum in three steps.
20 uggest an autostimulatory role for sigmaF in C. acetobutylicum, in contrast to the model organism for
21                                 For example, C. acetobutylicum increased from ~ 10 mM to ~ 17 mM, and
22 ed that the five orphan histidine kinases of C. acetobutylicum interact directly with Spo0A to contro
23                   Extractive fermentation of C. acetobutylicum is operated in fed-batch mode with a c
24                          Coexpression of the C. acetobutylicum maturation proteins with various algal
25 st PHX genes in all these genomes except for C. acetobutylicum (not PHX), and B. subtilis, and B. hal
26                                       When a C. acetobutylicum pSOL1 megaplasmid-deficient strain M5
27                         Novel members of the C. acetobutylicum Rex regulon were identified and experi
28 peron was subcloned into an Escherichia coli-C. acetobutylicum shuttle vector.
29                                          The C. acetobutylicum sigK deletion (DeltasigK) mutant was u
30 lases from Bacillus, Erwinia carotovora, and C. acetobutylicum species.
31 lysis of 824(pMSPOA) (a spo0A-overexpressing C. acetobutylicum strain with enhanced sporulation) agai
32 rtunities for developing a homobutanologenic C. acetobutylicum strain.
33 story of the development of omics studies of C. acetobutylicum, summarize the recent application of q
34                                Comparison of C. acetobutylicum to Bacillus subtilis reveals significa
35                      Inactivation of solR in C. acetobutylicum via homologous recombination yielded m
36                        Here the sigF gene in C. acetobutylicum was successfully disrupted and silence
37 nes identified in B. subtilis are missing in C. acetobutylicum, which suggests major differences in t