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Transductional analysis of chloramphenicol biosynthesis genes in Streptomyces venezuelae.

机译:委内瑞斯链霉菌中氯霉素生物合成基因的转导分析。

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摘要

Auxotrophs isolated from two chloramphenicol-nonproducing mutants of Streptomyces venezuelae included three requiring pyridoxal (Pxl-), VS248 (cml-11 pdx-2), VS253 (cml-11 pdx-3), and VS258 (cml-12 pdx-4), and one requiring thiosulfate, VS263 (cml-12 cys-28). Results of SV1-mediated transductions were consistent with the relative marker order cys-28-cml-12-cml-11-pdx-2,3,4,5, all of which were cotransducible and must therefore span less than 45 kilobases of DNA, the approximate length of DNA packaged by SV1. cys-28 was also cotransducible with arg-4 and arg-6, but arg and pdx were not cotransducible. Results of crosses with donors carrying any one of 11 cml mutations were consistent with the location of all cml mutations between cys-28 and pdx markers. Also, a new Pxl- auxotroph (pdx-6) and two new Cml- mutants were recovered after localized hydroxylamine mutagenesis of a cys-28 cml+ strain derived from VS263 by transduction.
机译:从委内瑞拉链霉菌的两个不产氯霉素的突变株中分离出的营养缺陷菌包括三个需要吡ido醛(Px1-),VS248(cml-11 pdx-2),VS253(cml-11 pdx-3)和VS258(cml-12 pdx-4) ,而另一种则需要硫代硫酸盐VS263(cml-12 cys-28)。 SV1介导的转导结果与相对标记顺序cys-28-cml-12-cml-11-pdx-2、3、4、5一致,所有这些都是共转导的,因此必须跨越少于45 kb的DNA ,即SV1包装的DNA的大约长度。 cys-28也可与arg-4和arg-6共转导,但arg和pdx不可共转导。与携带11个cml突变中任何一个的供体的杂交结果与cys-28和pdx标记之间所有cml突变的位置一致。同样,在通过转导作用对VS263衍生的cys-28 cml +菌株进行局部羟胺诱变后,回收了新的Pxl-营养缺陷型(pdx-6)和两个新的Cml-突变体。

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