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[大葱内生链霉菌线性质粒pYY8L端粒及内部复制起点的克隆与鉴定]

[Cloning and identification of telomere and internal origin of the endophytic Streptomyces linear plasmid pYY8L from Allium fistulosum].

作者信息

Yang Yong, Zhong Li, Tian Xinli, Cheng Qiuxiang, Chen Zhenhua, Qin Zhongjun

机构信息

Key laboratory of Synthetic Biology, Shanghai Institute of Plant Physiology and Ecology, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.

出版信息

Wei Sheng Wu Xue Bao. 2010 Apr;50(4):452-8.

Abstract

UNLABELLED

Strain 36R-2-1B was isolated from Allium fistulosum and identified as Streptomyces spp., harboring an approximate 280 kb linear plasmid designated pYY8L.

OBJECTIVE

Cloning, sequencing and analysis of telomere and internal replication origin of pYY8L.

METHODS

pYY8L telomere was cloned by a modified procedure--"alkaline treatment and enzyme digestion in gel". The internal replication origin of pYY8L was cloned by construction of a cosmid library and then subcloning.

RESULTS

An approximate 280 kb DNA band (pYY8L) of strain 36R-2-1B was detected by pulsed-field gel electrophoresis. The 152-bp telomere, containing six small palindromes and potentially forming complicated secondary structure, was cloned and sequenced. The replication origin of pYY8L was initially cloned on a cosmid and then sub-cloned as a 4891-bp autonomous replication sequence. This sequence was predicted to contain six genes, two of them resembling replication genes of Streptomyces linear plasmid SCP1, but their adjacent iterons were different.

CONCLUSION

New telomere and internal replication origin of Streptomyces linear plasmid pYY8L were cloned and identified. This is the first example of report on telomere and replication genes of linear plasmid from endophytic Streptomyces.

摘要

未标记

菌株36R - 2 - 1B从大葱中分离得到,鉴定为链霉菌属,携带一个约280 kb的线性质粒,命名为pYY8L。

目的

克隆、测序并分析pYY8L的端粒和内部复制起点。

方法

采用改良的“凝胶内碱处理和酶切”方法克隆pYY8L端粒。通过构建黏粒文库然后亚克隆来克隆pYY8L的内部复制起点。

结果

用脉冲场凝胶电泳检测到菌株36R - 2 - 1B的一条约280 kb的DNA条带(pYY8L)。克隆并测序了包含六个小回文序列且可能形成复杂二级结构的152 bp端粒。pYY8L的复制起点最初克隆到一个黏粒上,然后亚克隆为一个4891 bp的自主复制序列。该序列预计包含六个基因,其中两个类似于链霉菌线性质粒SCP1的复制基因,但它们相邻的迭代子不同。

结论

克隆并鉴定了链霉菌线性质粒pYY8L的新端粒和内部复制起点。这是关于内生链霉菌线性质粒端粒和复制基因报道的首个实例。

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