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来自白色链霉菌的编码O-去甲基嘌呤霉素O-甲基转移酶的dmpM基因的分子分析。

Molecular analysis of the dmpM gene encoding an O-demethyl puromycin O-methyltransferase from Streptomyces alboniger.

作者信息

Lacalle R A, Ruiz D, Jiménez A

机构信息

Centro de Biología Molecular (CSIC-UAM), Universidad Autónoma, Madrid, Spain.

出版信息

Gene. 1991 Dec 20;109(1):55-61. doi: 10.1016/0378-1119(91)90588-3.

Abstract

The nucleotide (nt) sequence of a 1332-bp fragment of Streptomyces alboniger DNA containing the gene (dmpM), which encodes an O-demethyl puromycin O-methyltransferase (DMPM), has been determined. The dmpM gene contains a 1131-nt open reading frame which encodes a polypeptide of Mr 40,303; this is consistent with the 44 +/- 2.5- and 160-kDa sizes of the DMPM monomer and its native form, respectively. The ATG start codon of dmpM is 50 bp downstream from the coding sequence of the gene (pac), which determines a puromycin N-acetyltransferase. S1 mapping experiments indicate that pac and dmpM are transcribed on a single transcript, which ends at least 500 nt downstream from the dmpM stop codon. The deduced amino acid sequence of DMPM shows significant similarities to those of a hydroxyindole O-methyltransferase, which is involved in the biosynthesis of melatonin by bovine pineal glands [Ishida et al., J. Biol. Chem. 262 (1987) 2895-2899], a hydroxyneurosporene methyltransferase, which is involved in carotenoid biosynthesis in the purple nonsulfur bacterium, Rhodobacter capsulatus [Armstrong et al., Mol. Gen. Genet. 216 (1989) 254-268] and two O-methyltransferases of the tetracenomycin biosynthesis pathway from Streptomyces glaucescens.

摘要

已确定白色链霉菌DNA的一个1332bp片段的核苷酸(nt)序列,该片段包含编码O-去甲基嘌呤霉素O-甲基转移酶(DMPM)的基因(dmpM)。dmpM基因包含一个1131nt的开放阅读框,编码一个Mr为40303的多肽;这分别与DMPM单体及其天然形式的44±2.5kDa和160kDa大小一致。dmpM的ATG起始密码子位于决定嘌呤霉素N-乙酰转移酶的基因(pac)编码序列下游50bp处。S1图谱实验表明,pac和dmpM转录在一个单一转录本上,该转录本在dmpM终止密码子下游至少500nt处结束。推导的DMPM氨基酸序列与羟吲哚O-甲基转移酶、羟神经孢烯甲基转移酶以及来自浅青紫链霉菌的四环霉素生物合成途径的两种O-甲基转移酶的氨基酸序列具有显著相似性,其中羟吲哚O-甲基转移酶参与牛松果体褪黑素的生物合成[石田等人,《生物化学杂志》262(1987)2895 - 2899],羟神经孢烯甲基转移酶参与紫色非硫细菌荚膜红细菌的类胡萝卜素生物合成[阿姆斯特朗等人,《分子遗传学与普通遗传学》216(1989)254 - 268]。

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