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肺炎支原体细胞黏附辅助蛋白HMW1和HMW3编码基因的并置

Juxtaposition of the genes encoding Mycoplasma pneumoniae cytadherence-accessory proteins HMW1 and HMW3.

作者信息

Krause D C, Lee K K

机构信息

Department of Microbiology, University of Georgia, Athens 30602.

出版信息

Gene. 1991 Oct 30;107(1):83-9. doi: 10.1016/0378-1119(91)90300-z.

Abstract

The loss and reacquisition of high-Mr (HMW) proteins, HMW1, 2, 3, 4 and 5, by Mycoplasma pneumoniae correlates with cytadherence phase variation. We are cloning and characterizing the genes encoding HMW1-5 to understand the mechanism regulating their coordinate expression. HMW1 was purified by polyacrylamide-gel electrophoresis. Amino acid (aa) sequence data were obtained from enzymatically generated peptide fragments from HMW1. A degenerate 17-mer probe synthesized based upon the aa sequence of one peptide clearly identified a single 4.75-kb BamHI fragment of M. pneumoniae DNA under stringent hybridization conditions. This fragment was cloned into pUC19 to generate pKV16. Restriction mapping of the 4.75-kb BamHI fragment in pKV16 revealed a possible overlap with the 9.4-kb EcoRI fragment containing the gene encoding protein HMW3. Southern blotting and reciprocal hybridization studies confirmed this overlap, establishing the juxtaposition of the genes encoding HMW1 and HMW3. Finally, physical mapping analysis by probing restriction fragments of M. pneumoniae DNA resolved by pulsed-field gel electrophoresis with the cloned genes encoding HMW1 and HMW3 revealed definitively that the hmw locus maps to a 106.8-kb ApaI fragment, rather than a 117.5-kb ApaI fragment, as had been reported previously for hmw3 [Krause and Mawn, J. Bacteriol. 172 (1990) 4790-4797].

摘要

肺炎支原体对高分子量(HMW)蛋白HMW1、2、3、4和5的丢失与重新获得,与细胞黏附相变相关。我们正在克隆和鉴定编码HMW1 - 5的基因,以了解调节它们协同表达的机制。通过聚丙烯酰胺凝胶电泳纯化HMW1。从HMW1酶促产生的肽片段获得氨基酸(aa)序列数据。基于一个肽的aa序列合成的简并17聚体探针,在严格杂交条件下明确鉴定出肺炎支原体DNA的一个单一4.75 kb BamHI片段。该片段被克隆到pUC19中以产生pKV16。对pKV16中4.75 kb BamHI片段的限制性图谱分析显示,它可能与包含编码蛋白HMW3的基因的9.4 kb EcoRI片段重叠。Southern印迹和反向杂交研究证实了这种重叠,确定了编码HMW1和HMW3的基因的并列关系。最后,通过用克隆的编码HMW1和HMW3的基因探测经脉冲场凝胶电泳分离的肺炎支原体DNA的限制性片段进行物理图谱分析,明确显示hmw基因座定位于一个106.8 kb的ApaI片段,而不是先前报道的hmw3所在的117.5 kb ApaI片段[克劳斯和莫恩,《细菌学杂志》172(1990)4790 - 4797]。

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