Nair R V, Green E M, Watson D E, Bennett G N, Papoutsakis E T
Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208, USA.
J Bacteriol. 1999 Jan;181(1):319-30. doi: 10.1128/JB.181.1.319-330.1999.
A gene (orf1, now designated solR) previously identified upstream of the aldehyde/alcohol dehydrogenase gene aad (R. V. Nair, G. N. Bennett, and E. T. Papoutsakis, J. Bacteriol. 176:871-885, 1994) was found to encode a repressor of the sol locus (aad, ctfA, ctfB and adc) genes for butanol and acetone formation in Clostridium acetobutylicum ATCC 824. Primer extension analysis identified a transcriptional start site 35 bp upstream of the solR start codon. Amino acid comparisons of SolR identified a potential helix-turn-helix DNA-binding motif in the C-terminal half towards the center of the protein, suggesting a regulatory role. Overexpression of SolR in strain ATCC 824(pCO1) resulted in a solvent-negative phenotype owing to its deleterious effect on the transcription of the sol locus genes. Inactivation of solR in C. acetobutylicum via homologous recombination yielded mutants B and H (ATCC 824 solR::pO1X) which exhibited deregulated solvent production characterized by increased flux towards butanol and acetone formation, earlier induction of aad, lower overall acid production, markedly improved yields of solvents on glucose, a prolonged solvent production phase, and increased biomass accumulation compared to those of the wild-type strain.
先前在乙醛/乙醇脱氢酶基因aad上游鉴定出的一个基因(orf1,现命名为solR)(R.V.奈尔、G.N.贝内特和E.T.帕普茨卡斯,《细菌学杂志》176:871 - 885,1994年),被发现编码丙酮丁醇梭菌ATCC 824中丁醇和丙酮形成相关的sol位点(aad、ctfA、ctfB和adc)基因的阻遏物。引物延伸分析确定了solR起始密码子上游35 bp处的一个转录起始位点。对SolR的氨基酸比较在蛋白质中心附近的C端一半区域鉴定出一个潜在的螺旋 - 转角 - 螺旋DNA结合基序,提示其具有调控作用。在菌株ATCC 824(pCO1)中过表达SolR会导致溶剂阴性表型,这是由于其对sol位点基因转录产生有害影响。通过同源重组使丙酮丁醇梭菌中的solR失活,产生了突变体B和H(ATCC 824 solR::pO1X),与野生型菌株相比,这些突变体表现出溶剂产生失调,其特征为丁醇和丙酮形成的通量增加、aad更早诱导、总酸产生降低、葡萄糖上溶剂产率显著提高、溶剂产生阶段延长以及生物量积累增加。