Suppr超能文献

灰色链霉菌中链霉素生物合成的基因簇:对包含主要抗性基因的中心区域的分析

Gene cluster for streptomycin biosynthesis in Streptomyces griseus: analysis of a central region including the major resistance gene.

作者信息

Distler J, Braun C, Ebert A, Piepersberg W

出版信息

Mol Gen Genet. 1987 Jun;208(1-2):204-10. doi: 10.1007/BF00330443.

Abstract

A central segment of a cluster of biosynthetic genes for the antibiotic streptomycin cloned from Streptomyces griseus was analysed for open reading frames, as well as for transcriptional and translational activity. The nucleotide sequence revealed two significant open reading frames, ORF1 and APH(6), orientated in opposite directions and with a spacer of 885 bp between the start codons. The first, ORF1, had a coding capacity of 38 kDa. One open reading frame, APH(6), was identified as the major resistance gene coding for streptomycin 6-phosphotransferase, a protein of 307 amino acid residues and 33 kDa. Sequence determination of the first 14 N-terminal amino acid residues of the purified APH(6) enzyme protein was in agreement with the proposed primary structure. The possible identity of the presumed gene product of ORF1 with an in vitro translated protein (apparent molecular weight 41 kDa) is discussed. Comparison of the two APH(6) genes from S. griseus and the hydroxystreptomycin-producing S. glaucescens (cf. Vögtli and Hütter 1987) revealed 75% nucleotide sequence homology in the coding region and 74% conservation of the polypeptide sequence. Two protein domains which are highly conserved in other antibiotic and protein phosphotransferases were detected.

摘要

对从灰色链霉菌克隆的抗生素链霉素生物合成基因簇的一个中央片段进行了开放阅读框以及转录和翻译活性分析。核苷酸序列显示有两个重要的开放阅读框,即ORF1和APH(6),它们方向相反,起始密码子之间间隔885 bp。第一个开放阅读框ORF1的编码能力为38 kDa。其中一个开放阅读框APH(6)被鉴定为编码链霉素6 - 磷酸转移酶的主要抗性基因,该酶蛋白由307个氨基酸残基组成,分子量为33 kDa。对纯化的APH(6)酶蛋白的前14个N端氨基酸残基进行的序列测定与所提出的一级结构一致。讨论了ORF1推测的基因产物与一种体外翻译蛋白(表观分子量为41 kDa)可能的同一性。对灰色链霉菌和产生羟基链霉素的浅蓝链霉菌的两个APH(6)基因进行比较(参见Vögtli和Hütter,1987),发现在编码区核苷酸序列同源性为75%,多肽序列保守性为74%。检测到在其他抗生素和蛋白质磷酸转移酶中高度保守的两个蛋白质结构域。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验