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由质粒ColA-CA31编码的裂解蛋白。基因序列与输出。

Lysis protein encoded by plasmid ColA-CA31. Gene sequence and export.

作者信息

Cavard D, Lloubès R, Morlon J, Chartier M, Lazdunski C

出版信息

Mol Gen Genet. 1985;199(1):95-100. doi: 10.1007/BF00327516.

Abstract

A gene, cal, coding for a polypeptide needed for the release of colicin A from Escherichia coli cells has been identified by transposon insertion. The cal gene was located on the ColA plasmid map adjacent to cai, the gene coding for colicin A immunity protein, and therefore 592 bases downstream from caa, the structural gene for colicin A. Transcription of cal is in the same direction as caa, that is in the opposite direction to cai. Its sequence has been determined and the predicted amino acid composition features a basic N-terminal end followed by a serie of hydrophobic residues similar to the signal sequence in precursors of exported proteins. The C-terminal part also contains a core of hydrophobic residues. The overall amino acid sequence of the cal protein is homologous to that of lytic proteins encoded by the related plasmids pColE1, and pCloDF13. The cal protein has been identified on urea-SDS-polyacrylamide gels by selective labelling with various radioactive amino acids and its synthesis is co-induced with that of colicin A. The cal protein undergoes slow processing with loss of the N-terminal "signal" region and the mature form is released into the medium together with colicin A.

摘要

通过转座子插入已鉴定出一个名为cal的基因,它编码从大肠杆菌细胞中释放大肠杆菌素A所需的一种多肽。cal基因位于ColA质粒图谱上,与编码大肠杆菌素A免疫蛋白的基因cai相邻,因此位于大肠杆菌素A结构基因caa下游592个碱基处。cal的转录方向与caa相同,即与cai相反。已确定其序列,预测的氨基酸组成特征是一个碱性的N末端,后面跟着一系列类似于输出蛋白前体中信号序列的疏水残基。C末端部分也含有疏水残基核心。cal蛋白的整体氨基酸序列与相关质粒pColE1和pCloDF13编码的裂解蛋白同源。通过用各种放射性氨基酸进行选择性标记,已在尿素-SDS-聚丙烯酰胺凝胶上鉴定出cal蛋白,其合成与大肠杆菌素A的合成共同被诱导。cal蛋白经历缓慢加工,N末端“信号”区域丢失,成熟形式与大肠杆菌素A一起释放到培养基中。

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