Matsui Toru, Saeki Hisashi, Shinzato Naoya, Matsuda Hitoshi
Center of Molecular Biosciences, University of the Ryukyus, 1 Sembaru, Okinawa 903-0213, Japan.
Curr Microbiol. 2006 Jun;52(6):445-8. doi: 10.1007/s00284-005-0237-1. Epub 2006 Apr 27.
Rhodococcus-E. coli shuttle vector pNC9501 was constructed using circular cryptic plasmid pNC903 from propene-degrading Rhodococcus ruber P-II-123-1. Sequence analysis of pNC903 revealed two open-reading frames encoding the replication proteins Reps A and B. In the amino acid sequence of the putative Rep B, a helix-turn-helix motif, which is responsible for the binding of DNA, was found. Sequencing of the upstream region of the putative Rep A and incompatibility tests revealed that pNC903 is a Mycobacterium-derived pAL5000-related plasmid. pNC9501 could also be transformed into Mycobacterium sp. showing good segregation stability (<0.1% plasmid loss/generation) in the absence of selective pressure.
利用来自降解丙烯的红球菌P-II-123-1的隐蔽环状质粒pNC903构建了红球菌-大肠杆菌穿梭载体pNC9501。对pNC903的序列分析揭示了两个编码复制蛋白Reps A和B的开放阅读框。在假定的Rep B的氨基酸序列中,发现了一个负责DNA结合的螺旋-转角-螺旋基序。对假定的Rep A上游区域的测序和不相容性测试表明,pNC903是一种源自分枝杆菌的与pAL5000相关的质粒。pNC9501也可以转化到分枝杆菌中,在没有选择压力的情况下显示出良好的分离稳定性(<0.1%质粒丢失/代)。