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肺炎链球菌插入序列IS1202的分离、特性鉴定及核苷酸序列分析

Isolation, characterization, and nucleotide sequence of IS1202, an insertion sequence of Streptococcus pneumoniae.

作者信息

Morona J K, Guidolin A, Morona R, Hansman D, Paton J C

机构信息

Department of Microbiology, Women's and Children's Hospital, North Adelaide, Australia.

出版信息

J Bacteriol. 1994 Jul;176(14):4437-43. doi: 10.1128/jb.176.14.4437-4443.1994.

Abstract

A comparative hybridization protocol was used to isolate a small segment of DNA present in the Streptococcus pneumoniae type 19F strain SSZ but absent from strain Rx1, a nonencapsulated derivative of the type 2 strain D39. This segment of DNA is a 1,747-bp insertion sequence, designated IS1202, flanked by 23-bp imperfect inverted repeats and containing a single open reading frame sufficient to encode a 54.4-kDa polypeptide. A 27-bp target sequence is duplicated at either end of the element. IS1202 is not related to any of the currently known insertion elements and is the first reported for S. pneumoniae. Although found predominantly in type 19F strains in up to five copies, it has also been shown to be present in the chromosomes of pneumococci belonging to other serotypes. One of the four IS1202 copies in the encapsulated strain SSZ is located 1,009 bp downstream of the dexB gene, and transformation studies reveal that it is also closely linked to the type 19F capsular polysaccharide synthesis (cps) locus.

摘要

采用比较杂交方案分离出肺炎链球菌19F型菌株SSZ中存在但2型菌株D39的非荚膜衍生物Rx1中不存在的一小段DNA。这段DNA是一个1747 bp的插入序列,命名为IS1202,两侧是23 bp的不完全反向重复序列,包含一个足以编码54.4 kDa多肽的单一开放阅读框。一个27 bp的靶序列在元件的两端重复。IS1202与目前已知的任何插入元件均无关联,是首次报道的肺炎链球菌插入元件。虽然主要在19F型菌株中发现,最多有5个拷贝,但也已证明它存在于其他血清型肺炎链球菌的染色体中。在荚膜菌株SSZ的4个IS1202拷贝中,有一个位于dexB基因下游1009 bp处,转化研究表明它也与19F型荚膜多糖合成(cps)位点紧密相连。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ec/205658/2d9dfadd9bb8/jbacter00032-0254-a.jpg

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