Hashiro Shuhei, Yasueda Hisashi
a Institute for Innovation , Ajinomoto Co., Inc ., Kawasaki , Japan.
Biosci Biotechnol Biochem. 2018 Dec;82(12):2212-2224. doi: 10.1080/09168451.2018.1508986. Epub 2018 Aug 18.
Cryptic plasmid pHM1519 is a rolling-circular replication mode plasmid of the pCG1 plasmid family in coryneform bacteria. The derived shuttle vector pPK4 is maintained at about 40-50 copies per chromosome in Corynebacterium glutamicum 2256 (ATCC 13869). We found that a mutation (designated copA1) within the repA gene encoding essential initiator protein RepA of the pHM1519-replicon increased the copy number of the mutant plasmid to about 800 copies per chromosome. The mutation was a single G to A base transition, which changed Gly to Glu at position 429 of the amino acid sequence of RepA. In silico secondary structure prediction of RepA suggested that Gly429 is situated in a disordered region in a helix-turn-helix motif, which is a typical DNA-binding domain. This study shows the first example of a high copy number of a C. glutamicum cryptic plasmid caused by an altered replication initiator protein.
隐蔽质粒pHM1519是棒状杆菌中pCG1质粒家族的滚环复制模式质粒。衍生的穿梭载体pPK4在谷氨酸棒杆菌2256(ATCC 13869)中以每条染色体约40 - 50个拷贝的数量维持。我们发现,编码pHM1519复制子必需起始蛋白RepA的repA基因内的一个突变(命名为copA1)将突变体质粒的拷贝数增加到每条染色体约800个拷贝。该突变是单个G到A的碱基转换,在RepA氨基酸序列的第429位将甘氨酸变为谷氨酸。对RepA的计算机辅助二级结构预测表明,甘氨酸429位于螺旋-转角-螺旋基序的无序区域,这是一个典型的DNA结合结构域。本研究展示了由改变的复制起始蛋白导致谷氨酸棒杆菌隐蔽质粒高拷贝数的首个实例。