首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Identification and characterization of Streptomyces ghanaensis ATCC14672 integration sites for three actinophage-based plasmids.
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Identification and characterization of Streptomyces ghanaensis ATCC14672 integration sites for three actinophage-based plasmids.

机译:三个基于放线菌的质粒的加纳链霉菌ATCC14672整合位点的鉴定和表征。

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摘要

Streptomyces ghanaensis produces the antibiotic moenomycin A, which is the only known direct inhibitor of bacterial peptidoglycan glycosyltransferases (transglycosylases). Recent progress in understanding moenomycin biosynthesis opens the door to the generation of novel moenomycins via biocombinatorial approaches. To realize the promise of such an approach, one needs better knowledge of the S. ghanaensis genome and diverse genetic tools for stable expression of recombinant constructs in this strain. In this respect, we report the intergeneric Escherichia coli-S. ghanaensis conjugal transfer of plasmids pRT801 and pSOK804 based on the actinophage BT1 and VWB integrase systems, respectively. The attB sites for these two plasmids and for pSET152 were characterized. In particular, sequencing revealed that a putative Arg-tRNA gene serves as an integration site for both phage VWB and pSAM2-like actinomycete integrative and conjugative element recently suggested to be widespread and functional in actinomycetes. The stability of the studied plasmids and their neutrality with respect to antibiotic production warrant their use for manipulations of S. ghanaensis genome.
机译:加纳链霉菌产生抗生素莫能霉素A,它是细菌肽聚糖糖基转移酶(转糖基酶)的唯一已知直接抑制剂。理解莫能霉素生物合成的最新进展为通过生物组合方法生成新的莫能霉素打开了大门。为了实现这种方法的前景,人们需要对加纳链球菌基因组有更好的了解,并需要多种遗传工具来稳定表达重组构建体。在这方面,我们报告了属间大肠杆菌-S。加纳纳人分别基于放线噬菌体BT1和VWB整合酶系统进行质粒pRT801和pSOK804的结合转移。表征了这两个质粒和pSET152的attB位点。特别地,测序揭示推定的Arg-tRNA基因作为噬菌体VWB和pSAM2样放线菌整合和结合元件的整合位点,最近被认为在放线菌中是广泛的和有功能的。所研究质粒的​​稳定性及其在抗生素生产方面的中性保证了它们可用于操作加纳链球菌基因组。

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