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编码核糖体DNA的枯草芽孢杆菌基因杂交模式的差异取决于DNA制备方法。

Differences in the hybridization pattern of Bacillus subtilis genes coding for rDNA depend on the method of DNA preparation.

作者信息

Waterhouse R N, Glover L A

机构信息

Department of Molecular and Cell Biology, Marischal College, University of Aberdeen, Scotland.

出版信息

Appl Environ Microbiol. 1993 Mar;59(3):919-21. doi: 10.1128/aem.59.3.919-921.1993.

DOI:10.1128/aem.59.3.919-921.1993
PMID:8097621
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC202209/
Abstract

Three different methods of DNA isolation (organic deproteinization, potassium acetate deproteinization, and the use of cetyltrimethylammonium bromide) have been used to prepare DNA from Bacillus subtilis. Subsequent hybridization with an rDNA probe (DNA coding for rRNA) produces different patterns, which mirror those previously reported to indicate an rDNA deletion.

摘要

已使用三种不同的DNA分离方法(有机脱蛋白法、醋酸钾脱蛋白法和使用十六烷基三甲基溴化铵)从枯草芽孢杆菌中制备DNA。随后与rDNA探针(编码rRNA的DNA)杂交产生不同的模式,这些模式与先前报道的表明rDNA缺失的模式一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed24/202209/873cf2ad3c2f/aem00032-0274-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed24/202209/f8cbb02dbdd5/aem00032-0274-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed24/202209/873cf2ad3c2f/aem00032-0274-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed24/202209/f8cbb02dbdd5/aem00032-0274-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed24/202209/873cf2ad3c2f/aem00032-0274-b.jpg

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本文引用的文献

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Structure and organization of rRNA operons in the region of the replication origin of the Bacillus subtilis chromosome.枯草芽孢杆菌染色体复制起点区域rRNA操纵子的结构与组织
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tRNA genes are found between 16S and 23S rRNA genes in Bacillus subtilis.在枯草芽孢杆菌中,转运RNA基因位于16S和23S核糖体RNA基因之间。
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Rapid DNA isolations for enzymatic and hybridization analysis.用于酶促和杂交分析的快速DNA分离
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