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Physical analysis and mapping of the Mycoplasma pneumoniae chromosome.

机译:肺炎支原体染色体的物理分析和作图。

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摘要

Field inversion gel electrophoresis was used for analysis of the chromosome of Mycoplasma pneumoniae. The restriction endonuclease SfiI (5'-GGCCNNNNNGGCC-3') generated 2 M. pneumoniae DNA fragments of approximately 437 and 357.5 kilobase pairs (kbp), whereas 13 restriction fragments ranging in size from 2.4 to 252.0 kbp resulted from digestion with ApaI (5'-GGGCCC-3'). Totaling the sizes of the individual restriction fragments from digestion with SfiI or ApaI yielded a genome size of 794.5 or 775.4 kbp, respectively. A physical map of the M. pneumoniae chromosome was constructed by using a combination of techniques that included analysis by sequential or partial restriction endonuclease digestions and use as hybridization probes of cloned M. pneumoniae DNA containing ApaI sites and hence overlapping adjacent ApaI fragments. Genetic loci for deoC, rrn, hmw3, and the P1 gene were identified by using cloned DNA to probe ApaI restriction fragment profiles.
机译:场反转凝胶电泳用于分析肺炎支原体的染色体。限制性核酸内切酶SfiI(5'-GGCCNNNNNGGCC-3')产生了2个肺炎支原体DNA片段,大约437和357.5千碱基对(kbp),而13个限制性片段的大小在2.4至252.0 kbp之间,是通过ApaI消化产生的(5 '-GGGCCC-3')。用SfiI或ApaI消化得到的各个限制性酶切片段的总大小分别为794.5 kbp或775.4 kbp。肺炎支原体染色体的物理图谱是使用多种技术组合构建的,这些技术包括通过顺序或部分限制性核酸内切酶消化进行分析,并用作克隆的含有ApaI位点并因此重叠的相邻ApaI片段的肺炎支原体DNA的杂交探针。 deoC,rrn,hmw3和P1基因的遗传位点是通过使用克隆的DNA探测ApaI限制性片段图谱来鉴定的。

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