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大肠杆菌D-丝氨酸脱氨酶区域的物理图谱:dsd结构基因与调控基因的连续性

Physical mapping of the Escherichia coli D-serine deaminase region: contiguity of the dsd structural and regulatory genes.

作者信息

Carothers A M, McFall E, Palchaudhuri S

出版信息

J Bacteriol. 1980 Apr;142(1):174-84. doi: 10.1128/jb.142.1.174-184.1980.

Abstract

The genes dsdA, dsdO, and dsdC have been located on a 3.0-kilobase pair (kb) fragment of the Escherichia coli chromosome by a combination of techniques. The loci were first cloned onto lambda and various plasmid vectors. dsd hybrid plasmids were then digested with restriction enzymes, and the fragments were recloned to test for the presence of dsdC or dsdA. In one case, a 4.2-kb restriction fragment containing the dsdA operon was used to form a heteroduplex with a well-defined lambda dsd deoxyribonucleic acid. The results show that dsdA, dsdO, and at least 0.6 kb of dsdC are present on this piece of deoxyribonucleic acid. On the basis of the mapping analysis and the molecular weight of D-serine deaminase, 1.9 kb of the 4.2-kb fragment is accounted for by the three dsd loci. We conclude that dsdO and dsdC are contiguous. A detailed dsd restriction map is presented.

摘要

通过多种技术相结合的方法,已将dsdA、dsdO和dsdC基因定位在大肠杆菌染色体的一个3.0千碱基对(kb)的片段上。这些基因座首先被克隆到λ噬菌体和各种质粒载体上。然后用限制性内切酶消化dsd杂交质粒,并将片段重新克隆以检测dsdC或dsdA的存在。在一个案例中,一个包含dsdA操纵子的4. kb限制性片段被用于与一个明确的λdsd脱氧核糖核酸形成异源双链体。结果表明,这段脱氧核糖核酸上存在dsdA、dsdO和至少0.6 kb的dsdC。根据图谱分析和D-丝氨酸脱氨酶的分子量,4.2 kb片段中的1.9 kb由三个dsd基因座占据。我们得出结论,dsdO和dsdC是相邻的。本文给出了详细的dsd限制性图谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5421/293924/2a909e50de58/jbacter00565-0189-a.jpg

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