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本文引用的文献

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Isolation and characterization of genes encoding two chitinase enzymes from Serratia marcescens.从粘质沙雷氏菌中分离和鉴定编码两种几丁质酶的基因。
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Cloning, sequence, and expression of a chitinase gene from a marine bacterium, Altermonas sp. strain O-7.来自海洋细菌交替单胞菌属O-7菌株的几丁质酶基因的克隆、测序及表达
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Identification of glutamic acid 204 and aspartic acid 200 in chitinase A1 of Bacillus circulans WL-12 as essential residues for chitinase activity.鉴定环状芽孢杆菌WL-12几丁质酶A1中的谷氨酸204和天冬氨酸200为几丁质酶活性的必需残基。
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Crystal structure of a bacterial chitinase at 2.3 A resolution.分辨率为2.3埃的细菌几丁质酶晶体结构。
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A bacteriophage lambda vector for cloning with BamHI and Sau3A.一种用于用BamHI和Sau3A进行克隆的λ噬菌体载体。
Gene. 1982 Dec;20(3):317-22. doi: 10.1016/0378-1119(82)90200-1.
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Nucleotide sequences of two cellulase genes from alkalophilic Bacillus sp. strain N-4 and their strong homology.嗜碱芽孢杆菌N-4菌株中两个纤维素酶基因的核苷酸序列及其高度同源性。
J Bacteriol. 1986 Nov;168(2):479-85. doi: 10.1128/jb.168.2.479-485.1986.
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Structure of the gene encoding chitinase D of Bacillus circulans WL-12 and possible homology of the enzyme to other prokaryotic chitinases and class III plant chitinases.环状芽孢杆菌WL-12几丁质酶D编码基因的结构以及该酶与其他原核几丁质酶和Ⅲ类植物几丁质酶可能的同源性。
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豚鼠气单胞菌chiA基因的克隆与一级结构

Cloning and primary structure of the chiA gene from Aeromonas caviae.

作者信息

Sitrit Y, Vorgias C E, Chet I, Oppenheim A B

机构信息

Otto Warburg Center for Agricultural Biotechnology, Faculty of Agriculture, Hebrew University, Rehovot, Israel.

出版信息

J Bacteriol. 1995 Jul;177(14):4187-9. doi: 10.1128/jb.177.14.4187-4189.1995.

DOI:10.1128/jb.177.14.4187-4189.1995
PMID:7608101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177160/
Abstract

The chiA gene from Aeromonas caviae encodes an extracellular chitinase, 865 amino acids long, that shows a high degree of similarity to chitinase A of Serratia marcescens. Expression in Escherichia coli yielded an enzymatically active protein from which a leader sequence was removed, presumably during transport of the enzyme across the cell membrane.

摘要

豚鼠气单胞菌的chiA基因编码一种胞外几丁质酶,该酶由865个氨基酸组成,与粘质沙雷氏菌的几丁质酶A具有高度相似性。在大肠杆菌中表达产生了一种具有酶活性的蛋白质,推测在该酶跨细胞膜转运过程中其前导序列被去除。