首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >The genes for benzene catabolism in Pseudomonas putida ML2 are flanked by two copies of the insertion element IS1489, forming a class-I-type catabolic transposon, Tn5542.
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The genes for benzene catabolism in Pseudomonas putida ML2 are flanked by two copies of the insertion element IS1489, forming a class-I-type catabolic transposon, Tn5542.

机译:恶臭假单胞菌ML2中苯分解代谢的基因两侧是插入元件IS1489的两个副本,形成了I型分解代谢转座子Tn5542。

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摘要

Two directly repeated sequences of the IS elements IS1489v1 and IS1489v2 flank the benzene dioxygenase (bedC1C2BA) and the cis-benzene dihydrodiol dehydrogenase (bedD) genes on the catabolic plasmid pHMT112 in Pseudomonas putida ML2, forming a Class-I-type composite transposon, Tn5542. Both IS1489v1 and IS1489v2 contain an identical 1371-bp open reading frame, tnpA, that is preceded by a possible ribosome binding site. The tnpA gene of IS1489v1 is bound by a pair of 40-bp imperfect inverted repeats while that of IS1489v2 is flanked only by the left inverted repeat. The tnpA gene codes for a putative 53-kDa polypeptide of 456 amino acids bearing similarity to transposases encoded on IS elements of P. alcaligenes, P. aeruginosa, P. stutzeri, and Serratia marcescens. The basic nature of the putative TnpA protein with a deduced pI of 8.93 is typical of IS-encoded transposases. Similar to other IS elements, an outward facing promoter was detected at the right end of IS1489v1. Experiments involving the suicide vector, pKNG101, failed to show transposition of Tn5542. Copyright 2000 Academic Press.
机译:IS元素IS1489v1和IS1489v2的两个直接重复序列位于恶臭假单胞菌ML2中分解代谢质粒pHMT112的苯二加氧酶(bedC1C2BA)和顺苯二氢二醇脱氢酶(bedD)基因的侧面,形成了I型复合转座子Tn5542 。 IS1489v1和IS1489v2都包含一个相同的1371 bp开放阅读框tnpA,其前面是可能的核糖体结合位点。 IS1489v1的tnpA基因被一对40 bp的不完美反向重复序列所结合,而IS1489v2的tnpA基因仅被左侧反向重复序列所侧接。 tnpA基因编码一个推测的456个氨基酸的53 kDa多肽,与在产碱假单胞菌,铜绿假单胞菌,斯图氏假单胞菌和粘质沙雷氏菌的IS元件上编码的转座酶相似。推定的pI为8.93的推定TnpA蛋白的基本性质是IS编码转座酶的典型特征。与其他IS元素相似,在IS1489v1的右端检测到朝外的启动子。涉及自杀载体pKNG101的实验未能显示Tn5542的转座。版权所有2000学术出版社。

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