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广宿主范围IncP-4质粒R1162:缺失和插入对质粒维持及宿主范围的影响

Broad-host-range IncP-4 plasmid R1162: effects of deletions and insertions on plasmid maintenance and host range.

作者信息

Meyer R, Laux R, Boch G, Hinds M, Bayly R, Shapiro J A

出版信息

J Bacteriol. 1982 Oct;152(1):140-50. doi: 10.1128/jb.152.1.140-150.1982.

Abstract

R1162 is an 8.7-kilobase (kb) broad-host-range replicon encoding resistance to streptomycin and sulfa drugs. In vitro deletion of 1.8-kb DNA between coordinates 3.0 and 5.3 kb did not affect plasmid maintenance, but a Tn1 insertion at coordinate 6.3 kb led to a recessive defect in plasmid maintenance. The only cis-acting region necessary for plasmid replication appears to lie between the Tn1 insertion at coordinate 6.3 kb and a second Tn1 insertion at coordinate 6.5 kb. All R1162 sequences between position 6.5 kb and the EcoRI site at coordinate 8.7/0 kb were dispensible for replication in Escherichia coli and Pseudomonas putida. Plasmids carrying insertions in a variety of restriction sites in an R1162::Tn1 derivative were unstable in P. putida but stable in E. coli. Tn5 insertions in R1162 showed a hot spot at coordinate 7.5 kb. A Tn5 insertion at coordinate 8.2 kb appeared to mark the 3' end of the streptomycin phosphotransferase coding sequence. All R1162::Tn5 derivatives showed specific instability in Pseudomonas strains but not in E. coli. The instability could be relieved by internal deletions of Tn5 sequences. In the haloaromatic-degrading Pseudomonas sp. strain B13, introduction of an unstable R1162::Tn5 plasmid led to loss of ability to utilize m-chlorobenzoate as a growth substrate. Our results showed that alteration of plasmid sequence organization in nonessential regions can result in restriction of plasmid host range.

摘要

R1162是一个8.7千碱基(kb)的广宿主范围复制子,编码对链霉素和磺胺类药物的抗性。在体外删除坐标3.0至5.3 kb之间的1.8 kb DNA并不影响质粒的维持,但在坐标6.3 kb处插入一个Tn1会导致质粒维持出现隐性缺陷。质粒复制所必需的唯一顺式作用区域似乎位于坐标6.3 kb处的Tn1插入位点与坐标6.5 kb处的第二个Tn1插入位点之间。在坐标6.5 kb与坐标8.7/0 kb处的EcoRI位点之间的所有R1162序列对于在大肠杆菌和恶臭假单胞菌中的复制都是可有可无的。在R1162::Tn1衍生物的各种限制性位点携带插入片段的质粒在恶臭假单胞菌中不稳定,但在大肠杆菌中稳定。R1162中的Tn5插入在坐标7.5 kb处显示出一个热点。在坐标8.2 kb处的Tn5插入似乎标记了链霉素磷酸转移酶编码序列的3'末端。所有R1162::Tn5衍生物在假单胞菌菌株中表现出特异性不稳定性,但在大肠杆菌中没有。通过内部删除Tn5序列可以缓解这种不稳定性。在降解卤代芳烃的假单胞菌属菌株B13中,引入不稳定的R1162::Tn5质粒导致利用间氯苯甲酸作为生长底物的能力丧失。我们的结果表明,非必需区域中质粒序列组织的改变可导致质粒宿主范围的限制。

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