Voordouw G, Brenner S
Eur J Biochem. 1986 Sep 1;159(2):347-51. doi: 10.1111/j.1432-1033.1986.tb09874.x.
The gene encoding the redox protein cytochrome c3 from Desulfovibrio vulgaris (Hildenborough) has been cloned using two synthetic oligonucleotides (one 17-mer and one 18-mer), designed to recognize the structural gene. Plasmid pCYC3 was derived from the clone and contains a 7.5 X 10(3)-base EcoRI-HindIII insert of D. vulgaris DNA in pUC9. A 674-base-pair fragment of this insert was sequenced with the dideoxy-chain-termination procedure and found to contain the entire structural gene encoding cytochrome c3 bracketed by apparent Escherichia coli consensus sequences for initiation and termination of transcription. The amino acid sequence of 107 residues, derived from protein sequencing [Trousil, E. B. and Campbell, L. L. (1974) J. Biol. Chem. 249, 386-393], is confirmed by the nucleic acid sequence, which shows in addition that it is preceded by a hydrophobic, positively charged signal sequence of 21 residues. This amino-terminal extension functions in the export of cytochrome c3, which is thought to reside in the periplasm of D. vulgaris.
利用两条合成寡核苷酸(一条17聚体和一条18聚体)克隆了编码普通脱硫弧菌(希登伯勒菌株)氧化还原蛋白细胞色素c3的基因,这两条寡核苷酸是设计用来识别该结构基因的。质粒pCYC3源自该克隆体,它在pUC9中含有一个7.5×10³碱基的普通脱硫弧菌DNA的EcoRI - HindIII插入片段。用双脱氧链终止法对该插入片段的一个674碱基对的片段进行了测序,发现它包含编码细胞色素c3的完整结构基因,其两侧是明显的大肠杆菌转录起始和终止共有序列。通过蛋白质测序[特鲁西尔,E. B.和坎贝尔,L. L.(1974年)《生物化学杂志》249,386 - 393]得到的107个残基的氨基酸序列,被核酸序列所证实,此外核酸序列还表明在其前面有一个由21个残基组成的疏水、带正电荷的信号序列。这个氨基末端延伸序列在细胞色素c3的输出中起作用,细胞色素c3被认为存在于普通脱硫弧菌的周质中。