Clennel A M, Johnston B, Rawlings D E
Department of Microbiology, University of Cape Town, Rondebosch, South Africa.
Appl Environ Microbiol. 1995 Dec;61(12):4223-9. doi: 10.1128/aem.61.12.4223-4229.1995.
A 3.5-kb region of plasmid pTF-FC2, which contains a transposon-like element designated Tn5467, has been sequenced, and its biological activity has been investigated. The transposon is bordered by two 38-bp inverted repeat sequences which have sequence identity in 37 of 38 and in 38 of 39 bp to the tnpA distal and tnpA proximal inverted repeats of Tn21, respectively. Within these borders, open reading frames with amino acid similarity to a glutaredoxin-like protein, a MerR regulatory protein, and a multidrug-resistant-membrane transport-like protein were found. The gene for the glutaredoxin-like protein was expressed in Escherichia coli and enabled growth of a glutathione-requiring E. coli trxA gshA mutant on minimal medium and the reduction of methionine sulfoxide to methionine. In addition, there were two regions which, when translated, had homology to 85% of the N-terminal region of the Tn21 resolvase (tnpR) and to 15% of the C terminus of the Tn21 transposase (tnpA). A region containing res-like sites was located immediately upstream of the partial tnpR gene. Neither the partial transposase nor the resolvase genes of Tn5467 were biologically active, but Tn5467 was transposed and resolved when the Tn21 transposase and resolvase were provided in trans. Tn5467 appears to be a defective transposon which belongs to the Tn21 subgroup of the Tn3 family.
质粒pTF-FC2的一个3.5kb区域已被测序,该区域包含一个类似转座子的元件Tn5467,并对其生物学活性进行了研究。该转座子由两个38bp的反向重复序列界定,它们分别与Tn21的tnpA远端和tnpA近端反向重复序列在38个碱基中的37个以及39个碱基中的38个具有序列同一性。在这些边界内,发现了与谷氧还蛋白样蛋白、MerR调控蛋白和多药耐药膜转运样蛋白具有氨基酸相似性的开放阅读框。谷氧还蛋白样蛋白的基因在大肠杆菌中表达,使需要谷胱甘肽的大肠杆菌trxA gshA突变体能够在基本培养基上生长,并将甲硫氨酸亚砜还原为甲硫氨酸。此外,有两个区域在翻译后与Tn21解离酶(tnpR)的N端区域的85%以及Tn21转座酶(tnpA)的C端的15%具有同源性。一个包含res样位点的区域位于部分tnpR基因的紧上游。Tn5467的部分转座酶基因和解离酶基因均无生物学活性,但当以反式提供Tn21转座酶和解离酶时,Tn5467可被转座和解离。Tn5467似乎是一个有缺陷的转座子,属于Tn3家族的Tn21亚组。