小单孢菌40027菌株质粒pJTU112复制区的克隆与序列特性
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国家自然科学基金(31070087,30570046);湖北省自然科学基金重点项目(2011CDA079,2008CDB076);国家大学生创新创业训练项目(GCX12012)


Cloning and sequence characterization of replication region in plasmid pJTU112 from Micoromonospora sp.40027
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Supported by the National Natural Science Foundation of China (31070087,30570046),by the Natural Science Foundation of Hubei province (2011CDA079,2008CDB076) and by the National College Students Innovative Entrepreneurial Training Program (GCX12012)

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    摘要:福堤霉素A 产生菌———小单孢菌40027菌株含有两个质粒pJTU101和pJTU112。【目的】对质粒pJTU112复制区进行克隆,并对质粒pJTU112复制区序列进行测定和分析。【方法】克隆质粒pJTU112的不同DNA片段导入消除质粒的小单孢菌40027菌株,通过复制功能的测定,确定质粒pJTU112的复制区,并进行测序和生物信息学分析。【结果】质粒pJTU112 的复制区定位在约4.7 kb的SacI-KpnI DNA片段上,测序和生物信息学分析表明:4.7 kb的SacI-KpnI DNA片段包含5个ORFs(open reading frames),其中pJTU112.1和pJTU112.2与质粒接合转移有关,pJTU112.3、pJTU112.4和pJTU112.5与质粒复制有关。【结论】质粒pJTU112的复制区定位在约4.7 kb的SacI-KpnI DNA片段上。

    Abstract:

    Abstract:Micoromonospora sp.40027,the producer of fortimicin A,harbors two plasmids pJTU101 and pJTU112.[Objective]Cloning and sequencing of replication region of pJTU112,analyzing replication region sequence of pJTU112.[Methods]Different fragments of pJTU112 were cloned and introduced by conjugation into Micromonospora sp. LXH20.The replication region of pJTU112 was identified.[Results]The replication region of pJTU112 was located in the 4.7 kb SacI-KpnI DNA fragment.DNA sequencing and analysis revealed that the 4.7 kb SacI-KpnI DNA fragment encoded five open reading frames.The pJTU112.1 and pJTU112.2 were related to plasmid conjugation,pJTU112.3,pJTU112.4 and pJTU112. 5 were related to plasmid conjugation.[Conclusion] The replication region of pJTU112 was located in the 4.7kb SacI-KpnI DNA fragment.

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耿旭梅,陈鑫,杨晓潼,郭佳,翟贵发,李晓华. 小单孢菌40027菌株质粒pJTU112复制区的克隆与序列特性. 微生物学报, 2013, 53(6): 623-627

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  • 收稿日期:2012-11-15
  • 最后修改日期:2013-01-09
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  • 在线发布日期: 2013-06-05
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