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利用红球菌属的靛蓝生产基因构建用于大肠杆菌的插入失活克隆载体。

Construction of an insertional-inactivation cloning vector for Escherichia coli using a Rhodococcus gene for indigo production.

作者信息

Hart S, Woods D R

机构信息

Department of Microbiology, University of Cape Town, Rondebosch, South Africa.

出版信息

J Gen Microbiol. 1992 Jan;138(1):205-9. doi: 10.1099/00221287-138-1-205.

Abstract

pSLH8, an insertional-inactivation cloning vector for Escherichia coli has been constructed by inserting a pigment gene (probably encoding an indole dioxygenase) from Rhodococcus sp. ATCC 21145 into pUC18. Wild-type E. coli colonies containing pSLH8 produce insoluble indigo and turn dark blue on unsupplemented LB agar. Insertion of DNA fragments into the unique BamHI, EcoRI, EcoRV, HindIII, PstI, SphI and SstI polylinker cloning sites disrupts the reading frame of the fully sequenced pigment gene and results in unpigmented colonies. pSLH8 may be an attractive alternative to pUC18 and similar plasmids because it does not require specifically mutated host strains or an expensive substrate for colour development.

摘要

pSLH8是一种用于大肠杆菌的插入失活克隆载体,它通过将红球菌属菌株ATCC 21145的一个色素基因(可能编码吲哚双加氧酶)插入pUC18构建而成。含有pSLH8的野生型大肠杆菌菌落会产生不溶性靛蓝,在未添加额外成分的LB琼脂平板上会变成深蓝色。将DNA片段插入独特的BamHI、EcoRI、EcoRV、HindIII、PstI、SphI和SstI多克隆位点克隆位点会破坏已完全测序的色素基因的阅读框,导致菌落无色素。pSLH8可能是pUC18和类似质粒的一个有吸引力的替代品,因为它不需要特定突变的宿主菌株或昂贵的显色底物。

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