López-Cabrera M, Pérez-González J A, Heinzel P, Piepersberg W, Jiménez A
Centro de Biología Molecular (CSIC and UAM), Universidad Autónoma, Madrid, Spain.
J Bacteriol. 1989 Jan;171(1):321-8. doi: 10.1128/jb.171.1.321-328.1989.
A gene (aacC7) encoding an aminocyclitol 3-N-acetyltransferase type VII [AAC(3)-VII] from Streptomyces rimosus forma paramomycinus NRRL 2455 was cloned in the Streptomyces plasmid pIJ702 and expressed in Streptomyces lividans 1326. Subcloning experiments located the aacC7 structural gene on a 1.05-kilobase DNA sequence. The direction of transcription of aacC7 was determined by using riboprobes synthesized in vitro from a DNA fragment internal to the gene. A DNA segment encoding the AAC(3)-VII activity and comprising 1,495 base pairs was sequenced. The aacC7 gene was located in an open reading frame of 864 base pairs that encoded a polypeptide of Mr 31,070, consistent with the Mr (32,000) of the AAC(3)-VII enzyme as determined by physicochemical methods. High-resolution S1 nuclease mapping suggested that transcription starts at or near the A residue of the ATG initiator codon. A DNA fragment from the 5' region of aacC7 had promoter activity in the promoter-probe plasmid pIJ486. The -10 and -35 regions of this fragment showed limited sequence resemblance to other Streptomyces promoters. The primary structure of the AAC(3)-VII enzyme showed strong homology with those of the AAC(3)-III and AAC(3)-IV enzymes encoded by plasmids in gram-negative bacterial genera. Upstream of the aacC7 gene was an open reading frame of 357 nucleotides which did not appear to be involved in controlling the expression of the aacC7 gene.
从龟裂链霉菌变铅青链霉菌亚种NRRL 2455中克隆出一个编码VII型氨基环醇3 - N - 乙酰基转移酶[AAC(3)-VII]的基因(aacC7),该基因克隆于链霉菌质粒pIJ702,并在变铅青链霉菌1326中表达。亚克隆实验将aacC7结构基因定位在一段1.05千碱基的DNA序列上。通过使用从该基因内部的DNA片段体外合成的核糖探针,确定了aacC7的转录方向。对编码AAC(3)-VII活性且包含1495个碱基对的DNA片段进行了测序。aacC7基因位于一个864碱基对的开放阅读框中,该阅读框编码一个分子量为31,070的多肽,这与通过物理化学方法测定的AAC(3)-VII酶的分子量(32,000)一致。高分辨率S1核酸酶图谱分析表明转录起始于ATG起始密码子的A残基处或其附近。来自aacC7 5'区域的一个DNA片段在启动子探针质粒pIJ486中具有启动子活性。该片段的 - 10和 - 35区域与其他链霉菌启动子的序列相似性有限。AAC(3)-VII酶的一级结构与革兰氏阴性菌属中质粒编码的AAC(3)-III和AAC(3)-IV酶的一级结构具有很强的同源性。在aacC7基因上游是一个357个核苷酸的开放阅读框,它似乎不参与控制aacC7基因的表达。