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嗜甲基白杆菌BG8的mxaAKL基因。

The mxaAKL genes of Methylobacter albus BG8.

作者信息

Arps P J, Speer B S, Kim Y M, Lidstrom M E

机构信息

Keck Laboratories, California Institute of Technology, Pasadena 91125, USA.

出版信息

Microbiology (Reading). 1995 Nov;141 ( Pt 11):2995-3004. doi: 10.1099/13500872-141-11-2995.

Abstract

The facultative methanol utilizer Methylobacterium extorquens AM1 contains at least three genes (mxaA, K and L) that encode functions involved in providing calcium to the holoenzyme of methanol dehydrogenase, the enzyme that oxidizes methanol to formaldehyde in this strain. Methane-utilizing bacteria (methanotrophs) also contain methanol dehydrogenase, and evidence suggests that similar methanol oxidation (Mox) functions may be present in some of these strains. DNA fragments from Methylobacterium extorquens AM1 specific to mxaA, mxaK and mxaL were isolated for use as hybridization probes against genomic digests of a variety of methanotrophic bacteria. Only the mxaL probe showed substantial hybridization, and it was used to identify and isolate an 8.5 kb HindIII fragment from Methylobacter albus BG8 (a Type I methanotroph). Hybridization of restriction digests of this fragment to individual probes for Methylobacterium extorquens AM1 mxaA, K and L indicated that the relative mxa gene order in Methylobacter albus BG8 is A-K-L. A T7 dual promoter/polymerase protein expression system indicated that five polypeptides are expressed from a 4.5 kb region of Methylobacter albus BG8 DNA in Escherichia coli, all transcribed in the same direction, and they apparently correspond to mxaACKDL. The functions of mxaC and mxaD are currently not known, but the order of mxaDL is reversed in Methylobacter albus BG8 compared to Methylobacterium extorquens AM1. When subclones of the Methylobacter albus BG8 fragment containing these genes were used as hybridization probes to genomic digests of methanotrophic bacteria, specific bands were detected that suggested a similar gene order in most cases. These data indicate that the mxaAKL region is relatively highly conserved in methanotrophs, and that in most cases the mxaAKL genes are grouped together in the same order as in the facultative methanol utilizer Methylobacterium extorquens AM1.

摘要

兼性甲醇利用菌扭脱甲基杆菌AM1含有至少三个基因(mxaA、K和L),这些基因编码的功能参与为甲醇脱氢酶全酶提供钙,甲醇脱氢酶是该菌株中将甲醇氧化为甲醛的酶。利用甲烷的细菌(甲烷营养菌)也含有甲醇脱氢酶,有证据表明其中一些菌株可能存在类似的甲醇氧化(Mox)功能。从扭脱甲基杆菌AM1中分离出特定于mxaA、mxaK和mxaL的DNA片段,用作针对多种甲烷营养菌基因组消化物的杂交探针。只有mxaL探针显示出大量杂交信号,它被用于从白色甲基杆菌BG8(一种I型甲烷营养菌)中鉴定和分离出一个8.5 kb的HindIII片段。该片段的限制性消化物与扭脱甲基杆菌AM1的mxaA、K和L的单个探针杂交表明,白色甲基杆菌BG8中mxa基因的相对顺序是A-K-L。一个T7双启动子/聚合酶蛋白表达系统表明,在大肠杆菌中,从白色甲基杆菌BG8 DNA的一个4.5 kb区域表达了五种多肽,它们都以相同方向转录,并且显然对应于mxaACKDL。mxaC和mxaD的功能目前尚不清楚,但与扭脱甲基杆菌AM1相比,白色甲基杆菌BG8中mxaDL的顺序是相反的。当将含有这些基因的白色甲基杆菌BG8片段的亚克隆用作甲烷营养菌基因组消化物的杂交探针时,检测到了特定条带,这表明在大多数情况下基因顺序相似。这些数据表明,mxaAKL区域在甲烷营养菌中相对高度保守,并且在大多数情况下,mxaAKL基因以与兼性甲醇利用菌扭脱甲基杆菌AM1相同的顺序聚集在一起。

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