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灰色链霉菌孢子形成相关的两个基因ssfR和ssgA的特性研究

Characterization of ssfR and ssgA, two genes involved in sporulation of Streptomyces griseus.

作者信息

Jiang H, Kendrick K E

机构信息

Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Bacteriol. 2000 Oct;182(19):5521-9. doi: 10.1128/JB.182.19.5521-5529.2000.

Abstract

In the presence of cefoxitin, which inhibits septum formation during sporulation, Streptomyces griseus is unable to sporulate, retaining the sonication sensitivity of nonsporulating hyphae. Cefoxitin- and sonication-resistant mutant SKK2600 was isolated and showed many morphological differences from its parental strain. A 3.6-kb DNA fragment that complemented the mutations of SKK2600 contained two open reading frames (ORFs), either of which could complement SKK2600. One ORF, designated ssfR, encoded a protein containing a potential DNA-binding helix-turn-helix motif close to its N terminus. SsfR is similar to members of a large family of transcriptional regulators, particularly IclR of Escherichia coli. The second ORF was identified as ssgA, a previously described sporulation gene from S. griseus (S. Kawamoto and J. C. Ensign, Actinomycetology 9:136-151, 1995). A point mutation of C to T seven nucleotides upstream of the UGA stop codon of ssfR was responsible for the phenotype of isolated mutant strain SKK2600. Surprisingly, this mutation should not change the primary structure of SsfR. The ssfR and ssgA disruption mutants were constructed and showed the "white" mutant phenotype, with some growth medium dependence. In addition, the ssfR null mutant sporulated ectopically in phosphate starvation medium.

摘要

在头孢西丁存在的情况下,头孢西丁会抑制孢子形成过程中的隔膜形成,灰色链霉菌无法形成孢子,保留了非孢子化菌丝对超声处理的敏感性。分离出了对头孢西丁和超声处理具有抗性的突变体SKK2600,它与其亲本菌株在许多形态上存在差异。一个能互补SKK2600突变的3.6 kb DNA片段包含两个开放阅读框(ORF),其中任何一个都能互补SKK2600。一个ORF,命名为ssfR,编码一种蛋白质,该蛋白质在其N端附近含有一个潜在的DNA结合螺旋-转角-螺旋基序。SsfR与一大类转录调节因子的成员相似,特别是大肠杆菌的IclR。第二个ORF被鉴定为ssgA,这是一个先前已描述的来自灰色链霉菌的孢子形成基因(S. Kawamoto和J. C. Ensign,《放线菌学》9:136 - 151,1995)。ssfR的UGA终止密码子上游七个核苷酸处的C到T点突变导致了分离出的突变菌株SKK2600的表型。令人惊讶的是,这种突变不应改变SsfR的一级结构。构建了ssfR和ssgA缺失突变体,它们表现出“白色”突变体表型,对某些生长培养基有依赖性。此外,ssfR缺失突变体在磷酸盐饥饿培养基中异位形成孢子。

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