Han Sung Ok, Yukawa Hideaki, Inui Masayuki, Doi Roy H
Section of Molecular and Cellular Biology, University of California, Davis, California 95616, USA.
J Bacteriol. 2003 Apr;185(8):2520-7. doi: 10.1128/JB.185.8.2520-2527.2003.
Transcription of the cellulosomal cellulase/hemicellulase genes of Clostridium cellulovorans has been investigated by Northern blot, reverse transcriptase PCR (RT-PCR), primer extension, and S1 nuclease analysis. Northern hybridizations revealed that the cellulosomal cbpA gene cluster is transcribed as polycistronic mRNAs of 8 and 12 kb. The 8-kb mRNA coded for cbpA and exgS, and the 12-kb mRNA coded for cbpA, exgS, engH, and engK. The sizes of the mRNAs were about 3 kb for engE, 1.8 kb for manA, 2.7 kb for xynA, and 4 kb for pelA, indicating monocistronic transcription of these genes. Primer extension and S1 nuclease analysis of C. cellulovorans RNA showed that the transcriptional start sites of cbpA, engE, manA, and hbpA were located 233, 97, 64, and 61 bp upstream from the first nucleotide of each of the respective translation initiation codons. Alignment of the cbpA, engE, manA, and hbpA promoter regions provided evidence for highly conserved sequences that exhibited strong similarity to the sigma(A) consensus promoter sequences of gram-positive bacteria.
通过Northern印迹、逆转录酶PCR(RT-PCR)、引物延伸和S1核酸酶分析,对食纤维梭菌的纤维小体纤维素酶/半纤维素酶基因的转录进行了研究。Northern杂交显示,纤维小体cbpA基因簇转录为8 kb和12 kb的多顺反子mRNA。8 kb的mRNA编码cbpA和exgS,12 kb的mRNA编码cbpA、exgS、engH和engK。engE的mRNA大小约为3 kb,manA为1.8 kb,xynA为2.7 kb,pelA为4 kb,表明这些基因是单顺反子转录。对食纤维梭菌RNA的引物延伸和S1核酸酶分析表明,cbpA、engE、manA和hbpA的转录起始位点分别位于各自翻译起始密码子第一个核苷酸上游233、97、64和61 bp处。cbpA、engE、manA和hbpA启动子区域的比对为高度保守序列提供了证据,这些序列与革兰氏阳性菌的sigma(A)共有启动子序列具有很强的相似性。