首页> 美国卫生研究院文献>Journal of Bacteriology >The bldC Developmental Locus of Streptomyces coelicolor Encodes a Member of a Family of Small DNA-Binding Proteins Related to the DNA-Binding Domains of the MerR Family
【2h】

The bldC Developmental Locus of Streptomyces coelicolor Encodes a Member of a Family of Small DNA-Binding Proteins Related to the DNA-Binding Domains of the MerR Family

机译:coelicolor链霉菌的bldC发育轨迹编码与MerR家族的DNA结合域相关的小DNA结合蛋白家族的成员。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The bldC locus, required for formation of aerial hyphae in Streptomyces coelicolor, was localized by map-based cloning to the overlap between cosmids D17 and D25 of a minimal ordered library. Subcloning and sequencing showed that bldC encodes a member of a previously unrecognized family of small (58- to 78-residue) DNA-binding proteins, related to the DNA-binding domains of the MerR family of transcriptional activators. BldC family members are found in a wide range of gram-positive and gram-negative bacteria. Constructed ΔbldC mutants were defective in differentiation and antibiotic production. They failed to form an aerial mycelium on minimal medium and showed severe delays in aerial mycelium formation on rich medium. In addition, they failed to produce the polyketide antibiotic actinorhodin, and bldC was shown to be required for normal and sustained transcription of the pathway-specific activator gene actII-orf4. Although ΔbldC mutants produced the tripyrrole antibiotic undecylprodigiosin, transcripts of the pathway-specific activator gene (redD) were reduced to almost undetectable levels after 48 h in the bldC mutant, in contrast to the bldC+ parent strain in which redD transcription continued during aerial mycelium formation and sporulation. This suggests that bldC may be required for maintenance of redD transcription during differentiation. bldC is expressed from a single promoter. S1 nuclease protection assays and immunoblotting showed that bldC is constitutively expressed and that transcription of bldC does not depend on any of the other known bld genes. The bldC18 mutation that originally defined the locus causes a Y49C substitution that results in instability of the protein.
机译:通过基于图的克隆,将在天蓝色链霉菌中形成气生菌丝所需的bldC基因座定位到最小有序文库的粘粒D17和D25之间的重叠。亚克隆和测序表明,bldC编码一个先前未被识别的小(58至78个残基)DNA结合蛋白家族成员,该家族与转录激活因子MerR家族的DNA结合域有关。在广泛的革兰氏阳性和革兰氏阴性细菌中发现BldC家族成员。构建的ΔbldC突变体在分化和抗生素产生方面存在缺陷。他们未能在基本培养基上形成气生菌丝体,并在丰富培养基上显示出严重的气生菌丝形成延迟。此外,他们无法产生聚酮类抗生素放线菌丝蛋白,并且bldC被证明是途径特异性激活基因actII-orf4正常和持续转录所必需的。尽管ΔbldC突变体产生了三吡咯抗生素十一烷基prodigiosin,但与bldC + 亲本菌株相比,在bldC突变体中,途径特异性激活基因(redD)的转录本在48 h后降低到几乎不可检测的水平。在气生菌丝形成和孢子形成过程中,redD转录持续进行。这表明在分化过程中可能需要bldC来维持redD转录。 bldC由单个启动子表达。 S1核酸酶保护试验和免疫印迹表明,bldC是组成型表达的,并且bldC的转录不依赖于任何其他已知的 bld 基因。最初定义基因座的 bldC18 突变引起Y49C取代,导致蛋白质不稳定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号