首页> 外文期刊>Journal of Biotechnology >Transcriptional analysis and proteomics of the holomycin gene cluster in overproducer mutants of Streptomyces clavuligerus
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Transcriptional analysis and proteomics of the holomycin gene cluster in overproducer mutants of Streptomyces clavuligerus

机译:克拉维链霉菌超生产突变体中holomycin基因簇的转录分析和蛋白质组学。

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Expression of the holomycin biosynthesis genes (hlm) has been studied in the wild type strain Streptomyces clavuligerus ATCC 27064 and holomycin overproducer mutants. RT-PCR transcription analysis of S. clavuligerus oppA2::aph showed a higher transcription of the hlmA, B, C, D, E, F, G, H, I and hlmL genes, a slightly lower expression for hlmK and no significant differences for the transcription of the two putative regulatory genes, hlmM and hlmJ, in relation to the wild type strain. Accordingly, protein spots corresponding to HlmD, HlmF and HlmG, which were barely detectable in the wild type strain, were present in high amounts in the holomycin overproducer S. clavuligerus oppA2::aph proteome. Transcription start point analysis of the hlm genes revealed that the annotated sequences in the databases for several hlm genes were incorrect. The hlm cluster was introduced into Streptomyces coelicolor M1154 and holomycin production by S. coelicolor M1154 [pVR-hol1] was validated by bioassays and confirmed by HPLC analysis and mass spectrometry. Heterologous holomycin production by the S. coelicolor transformant is 500-fold lower than in S. clavuligerus oppA2::aph. The transformant S. coelicolor M1154 [pVR-hol1] shows holomycin sensitivity to 100 μg/ml, similar to that of the parental S. coelicolor M1154 strain, suggesting that heterologous expression in S. coelicolor might be toxic due to the lack of an holomycin resistance gene in this host strain.
机译:已经在野生型菌株Streptomyces clavuligerus ATCC 27064和holomycin生产过量的突变体中研究了holomycin生物合成基因(hlm)的表达。棒状链霉菌oppA2 :: aph的RT-PCR转录分析显示hlmA,B,C,D,E,F,G,H,I和hlmL基因的转录较高,而hlmK的表达略低,并且无显着差异与野生型菌株有关的两个假定的调节基因hlmM和hlmJ的转录。因此,在野生型菌株中几乎检测不到的与HlmD,HlmF和HlmG相对应的蛋白质斑点在holomycin生产过量的S. clavuligerus oppA2 :: aph蛋白质组中大量存在。对hlm基因的转录起点分析表明,数据库中几个hlm基因的注释序列不正确。将hlm簇引入链霉菌M1154中,并通过生物测定法验证由链霉菌M1154 [pVR-hol1]生产的全息霉素,并通过HPLC分析和质谱法进行确认。 Coelicolor S. coelicolor转化株产生的异源整霉素比S. clavuligerus oppA2 :: aph低500倍。转化体coelicolor M1154 [pVR-hol1]表现出对霉素的敏感性为100μg/ ml,类似于亲本S. coelicolor M1154菌株,这表明由于缺乏holomycin,coelicolor S. coelicolor中的异源表达可能是有毒的该宿主菌株中的抗性基因。

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