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idsA的分离与鉴定:来自嗜热自养甲烷杆菌的短链异戊二烯基二磷酸合酶基因

Isolation and characterization of idsA: the gene for the short chain isoprenyl diphosphate synthase from Methanobacterium thermoautotrophicum.

作者信息

Chen A, Poulter C D

机构信息

Department of Chemistry, University of Utah, Salt Lake City 84112.

出版信息

Arch Biochem Biophys. 1994 Nov 1;314(2):399-404. doi: 10.1006/abbi.1994.1459.

Abstract

The gene that encodes the bifunctional short chain isoprenyl diphosphate synthase (idsA) for synthesis of farnesyl diphosphate and geranylgeranyl diphosphate in Methanobacterium thermoautotrophicum, a strict archaebacterial anaerobe, was isolated from a genomic DNA library by colony-lift hybridization and sequenced. Amino acid sequences were obtained for the N-terminus of the enzyme and for internal peptide fragments generated by proteolysis and treatment with cyanogen bromide. Degenerate primers based on the amino acid sequences were used in PCR to synthesize a 220-bp probe from genomic DNA. The probe was radiolabeled and used to isolate idsA. DNA sequencing revealed a 975-bp open reading frame located within an operon. The encoded 325-amino-acid protein contained five conserved regions found in eubacterial and eukaryotic farnesyl diphosphate and geranylgeranyl diphosphate synthases, including aspartate-rich motifs commonly found in prenyltransferases.

摘要

从严格厌氧的古细菌嗜热自养甲烷杆菌中分离出了编码双功能短链异戊二烯基二磷酸合酶(idsA)的基因,该酶用于合成法呢基二磷酸和香叶基香叶基二磷酸。通过菌落杂交从基因组DNA文库中分离出该基因并进行测序。获得了该酶N端以及经蛋白酶水解和溴化氰处理产生的内部肽片段的氨基酸序列。基于这些氨基酸序列设计了简并引物,用于通过PCR从基因组DNA合成一个220 bp的探针。该探针经放射性标记后用于分离idsA。DNA测序显示一个975 bp的开放阅读框位于一个操纵子内。编码的325个氨基酸的蛋白质含有在真细菌和真核生物的法呢基二磷酸和香叶基香叶基二磷酸合酶中发现的五个保守区域,包括在异戊二烯基转移酶中常见的富含天冬氨酸的基序。

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