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本文引用的文献

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Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
2
A genetic approach to characterizing complex promoters in E. coli.一种用于表征大肠杆菌中复杂启动子的遗传学方法。
Cell. 1981 Feb;23(2):307-8. doi: 10.1016/0092-8674(81)90125-2.
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Use of cir-lac operon fusions to study transcriptional regulation of the colicin Ia receptor in Escherichia coli K-12.利用cir-lac操纵子融合来研究大肠杆菌K-12中大肠菌素Ia受体的转录调控。
J Bacteriol. 1981 Jan;145(1):647-50. doi: 10.1128/jb.145.1.647-650.1981.
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Phosphate-controlled gene expression in Escherichia coli K12 using Mudl-directed lacZ fusions.利用Mudl定向的lacZ融合技术研究大肠杆菌K12中磷酸盐控制的基因表达。
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5
Spontaneous tandem genetic duplications in Salmonella typhimurium arise by unequal recombination between rRNA (rrn) cistrons.鼠伤寒沙门氏菌中的自发串联基因重复通过rRNA(rrn)顺反子之间的不等交换产生。
Proc Natl Acad Sci U S A. 1981 May;78(5):3113-7. doi: 10.1073/pnas.78.5.3113.
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DNA-damaging agents stimulate gene expression at specific loci in Escherichia coli.DNA损伤剂刺激大肠杆菌中特定基因座的基因表达。
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7
Bacteriophage P22 as a vector for Mu mutagenesis in Salmonella typhimurium: isolation of nad-lac and pnc-lac gene fusions.噬菌体P22作为鼠伤寒沙门氏菌中Mu诱变的载体:nad-lac和pnc-lac基因融合体的分离
J Bacteriol. 1982 Nov;152(2):959-62. doi: 10.1128/jb.152.2.959-962.1982.
8
Replication of mini-Mu prophage DNA.微小 Mu 原噬菌体 DNA 的复制
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Proc Natl Acad Sci U S A. 1984 Jan;81(2):535-9. doi: 10.1073/pnas.81.2.535.

Mu d1(Amp Lac)的条件性转座缺陷衍生物

Conditionally transposition-defective derivative of Mu d1(Amp Lac).

作者信息

Hughes K T, Roth J R

出版信息

J Bacteriol. 1984 Jul;159(1):130-7. doi: 10.1128/jb.159.1.130-137.1984.

DOI:10.1128/jb.159.1.130-137.1984
PMID:6330026
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC215603/
Abstract

A Mu d1 derivative is described which is useful for genetic manipulation of Mu-lac fusion insertions. A double mutant of the specialized transducing phage Mu d1(Amp Lac c62ts) was isolated which is conditionally defective in transposition ability. The Mu d1 derivative, designated Mu d1-8(Tpn[Am] Amp Lac c62ts), carries mutations which virtually eliminate transposition in strains lacking an amber suppressor. In such strains, the Mu d1-8 prophage behaves like a standard transposon. It can be moved from one strain of Salmonella typhimurium to another by the general transducing phage P22 with almost 100% inheritance of the donor insertion mutation. When introduced into a recipient carrying supD, supE, or supF, 89 to 94% of the Ampr transductants were transpositions of the donor Mu d1-8, from the transduced fragment into new sites. The stability of Mu d1-8 in a wild-type, suppressor-free background was sufficient to permit use of the fusion to select constitutive mutations without prior isolation of deletions to stabilize the fusion. Fusion strains could be grown at elevated temperature without induction of the Mu d prophage. The transposition defect of Mu d1-8 was corrected by a plasmid carrying the Mu A and B genes.

摘要

描述了一种Mu d1衍生物,它可用于Mu - lac融合插入的基因操作。分离出了专门转导噬菌体Mu d1(Amp Lac c62ts)的双突变体,其转座能力存在条件缺陷。命名为Mu d1 - 8(Tpn[Am] Amp Lac c62ts)的Mu d1衍生物携带的突变几乎消除了在缺乏琥珀抑制子的菌株中的转座。在这样的菌株中,Mu d1 - 8原噬菌体的行为类似于标准转座子。它可以通过通用转导噬菌体P22从一株鼠伤寒沙门氏菌转移到另一株,供体插入突变的遗传率几乎为100%。当导入携带supD、supE或supF的受体时,89%至94%的Amp r转导子是供体Mu d1 - 8从转导片段转移到新位点的转座。Mu d1 - 8在野生型、无抑制子背景下的稳定性足以允许利用该融合来选择组成型突变,而无需事先分离缺失来稳定融合。融合菌株可以在高温下生长而不诱导Mu d原噬菌体。携带Mu A和B基因的质粒纠正了Mu d1 - 8的转座缺陷。