Shaw W V, Brenner D G, LeGrice S F, Skinner S E, Hawkins A R
FEBS Lett. 1985 Jan 1;179(1):101-6. doi: 10.1016/0014-5793(85)80200-3.
The nucleotide sequence of the inducible chloramphenicol acetyltransferase gene (cat) of Staphylococcus aureus plasmid pC221 has been determined. The deduced primary structure for the 215 residue polypeptide (25.9 kDa) is in agreement with partial amino acid sequence data on the purified protein, previously designated as the type C variant of CAT. In common with the inducible cat elements of pC194 and B. pumilus, the 5' non-coding region of the cat of pC221 contains an inverted complementary repeat ('stem-loop' or 'hairpin') which may sequester the predicted ribosome bonding site of the mRNA. The likely transcription initiation site has been determined in vitro using purified B. subtilis RNA polymerase. Recombinant plasmids carrying the cat of pC221 on a 1156 bp TaqI fragment are expressed inefficiently in Escherichia coli, wherein induction is both poor and orientation-specific.
已测定金黄色葡萄球菌质粒pC221中可诱导氯霉素乙酰转移酶基因(cat)的核苷酸序列。推导得到的215个残基多肽(25.9 kDa)的一级结构与先前鉴定为氯霉素乙酰转移酶C型变体的纯化蛋白的部分氨基酸序列数据一致。与pC194和短小芽孢杆菌的可诱导cat元件一样,pC221的cat的5'非编码区包含一个反向互补重复序列(“茎环”或“发夹”),它可能会隔离mRNA的预测核糖体结合位点。使用纯化的枯草芽孢杆菌RNA聚合酶在体外确定了可能的转录起始位点。携带pC221的cat的1156 bp TaqI片段的重组质粒在大肠杆菌中表达效率低下,其中诱导作用既差又具有方向特异性。