Suppr超能文献

肺炎支原体染色体的物理分析与图谱绘制。

Physical analysis and mapping of the Mycoplasma pneumoniae chromosome.

作者信息

Krause D C, Mawn C B

机构信息

Department of Microbiology, University of Georgia, Athens 30602.

出版信息

J Bacteriol. 1990 Sep;172(9):4790-7. doi: 10.1128/jb.172.9.4790-4797.1990.

Abstract

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.

摘要

采用脉冲场反转凝胶电泳分析肺炎支原体的染色体。限制性内切酶SfiI(5'-GGCCNNNNNGGCC-3')产生了两条大小约为437和357.5千碱基对(kbp)的肺炎支原体DNA片段,而用ApaI(5'-GGGCCC-3')消化则产生了13条大小从2.4至252.0 kbp不等的限制性片段。分别将用SfiI或ApaI消化产生的各个限制性片段的大小相加,得出基因组大小分别为794.5 kbp或775.4 kbp。通过综合运用多种技术构建了肺炎支原体染色体的物理图谱,这些技术包括顺序或部分限制性内切酶消化分析,以及使用含有ApaI位点从而与相邻ApaI片段重叠的克隆肺炎支原体DNA作为杂交探针。通过使用克隆DNA探测ApaI限制性片段图谱,确定了deoC、rrn、hmw3和P1基因的遗传位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdda/213132/1fb49f796c7b/jbacter00123-0062-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验