综述

细菌几丁质酶基因的表达调控

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  • 1. 南开大学微生物学系, 天津 300071 2. 分子微生物学与技术教育部重点实验室, 天津 300071

收稿日期: 2011-03-31

  修回日期: 2011-06-14

  网络出版日期: 2011-10-25

基金资助

国家自然科学基金项目(编号:30971957)资助

Regulation of chitinase genes expression in bacteria

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  • 1. Department of Microbiology, Nankai University, Tianjin 300071, China 2. Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Tianjin 300071, China

Received date: 2011-03-31

  Revised date: 2011-06-14

  Online published: 2011-10-25

摘要

几丁质酶可以降解几丁质, 广泛存在于各类微生物中。几丁质的降解产物几丁寡糖在医药、食品及农业生防领域有很重要的应用价值及广泛的应用前景。细菌在利用几丁质时, 需要先分泌几丁质酶, 将几丁质降解成几丁寡糖或单体, 再通过特异的转运系统送进细胞而被利用。胞内的几丁质降解产物作为特定的信号分子, 可以激活或阻遏相应chi基因的转录, 从而影响细菌几丁质酶的合成。在各种调节蛋白及应答元件的参与下, 细菌几丁质酶的合成受到精密的控制。文章以链霉菌和大肠杆菌为代表综述了细菌在转运系统和基因表达两个层面上控制几丁质酶合成的最新研究进展。

本文引用格式

谢池楚,贾海云,陈月华 . 细菌几丁质酶基因的表达调控[J]. 遗传, 2011 , 33(10) : 1029 -1038 . DOI: 10.3724/SP.J.1005.2011.01029

Abstract

Chitinases, which can hydrolyze chitin, occur in a wide range of microorganisms including viruses, bacteria, and fungi. The derivatives of chitin are potentially useful in several areas such as food processing, medicines, and biological control in agriculture. Some bacteria can uptake and utilize chitin as carbon source by secreting chitinase. The chitin is degraded into chito-oligosaccharides [(GlcNAc)n] or N-acetylglucosamine (GlcNAc) by chitinases, and then the chitin derivatives are transferred into cells by specific transport systems of bacteria. The intracellular chitin derivatives activate or suppress the transcription of a series of chi genes and affect the amount of chitinase. The expression of chitinase genes are strictly regulated by various regulatory factors and responsive cis-acting elements. The present review will focus on the transport system and the regulation of chitinase genes expression in bacteria.

参考文献

[1] Khoushab F, Yamabhai M. Chitin research revisited. Mar Drugs, 2010, 8(7): 1988-2012.
[2] Zhao Y, Park RD, Muzzarelli RAA. Chitin deacetylases: properties and applications. Mar Drugs, 2010, 8(1): 24-46.
[3] Maillet F, Poinsot V, André O, Puech-Pagès V, Haouy A, Gueunier M, Cromer L, Giraudet D, Formey D, Niebel A, Martinez EA, Driguez H, Bécard G, Dénarié J. Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. Nature, 2011, 469(7328): 58-63.
[4] Felse PA, Panda T. Regulation and cloning of microbial chitinase genes. Appl Microbiol Biotechnol, 1999, 51(2): 141-151.
[5] Miyashita K, Fujii T, Saito A. Induction and repression of a Streptomyces lividans chitinase gene promoter in response to various carbon sources. Biosci Biotechnol Biochem, 2000, 64(1): 39-43.
[6] 谢池楚, 陈月华, 蔡峻, 刘传, 陈艳玲. Bt几丁质酶的基础表达及诱导合成的多态现象. 生物工程学报, 2010, 26(11): 1532-1538.
[7] Saito A, Fujii T, Shinya T, Shibuya N, Ando A, Miyashita K. The msiK gene, encoding the ATP-hydrolysing component of N, N'-diacetylchitobiose ABC transporters, is essential for induction of chitinase production in Streptomyces coelicolor A3(2). Microbiol-Sgm, 2008, 154(Pt 11): 3358-3365.
[8] Hirano T, Kadokura K, Ikegami T, Shigeta Y, Kumaki Y, Hakamata W, Oku T, Nishio T. Heterodisaccharide 4-O-(N-acetyl-β-D-glucosaminyl)-D-glucosamine is a specific inducer of chitinolytic enzyme production in Vibrios harboring chitin oligosaccharide deacetylase genes. Glycobiology, 2009, 19(9): 1046-1053.
[9] Toratani T, Shoji T, Ikehara T, Suzuki K, Watanabe T. The importance of chitobiase and N-acetylglucosamine (GlcNAc) uptake in N, N'-diacetylchitobiose
[(GlcNAC)2] utilization by Serratia marcescens 2170. Microbiology, 2008, 154(Pt 5): 1326-1332.
[10] 马婉晴, 章珍, 刘悦琳, 王华忠. 大肠杆菌分解代谢产物阻遏效应研究进展. 遗传, 2010, 32(6): 571-576.
[11] Plumbridge J. Regulation of PTS gene expression by the homologous transcriptional regulators, Mlc and NagC, in Escherichia coli (or how two similar repressors can behave differently). J Mol Microbiol Biotechnol, 2001, 3(3): 371-380.
[12] Nothaft H, Rigali S, Boomsma B, Swiatek M, McDowall KJ, van Wezel GP, Titgemeyer F. The permease gene nagE2 is the key to N-acetylglucosamine sensing and utilization in Streptomyces coelicolor and is subject to multi-level control. Mol Microbiol, 2010, 75(5): 1133-1144.
[13] Plumbridge J, Pellegrini O. Expression of the chitobiose operon of Escherichia coli is regulated by three transcription factors: NagC, ChbR and CAP. Mol Microbiol, 2004, 52(2): 437-449.
[14] Colson S, van Wezel GP, Craig M, Noens EEE, Nothaft H, Mommaas AM, Titgemeyer F, Joris B, Rigali S. The chitobiose-binding protein, DasA, acts as a link between chitin utilization and morphogenesis in Streptomyces coelicolor. Microbiology, 2008, 154(Pt 2): 373-382.
[15] Meibom KL, Li XB, Nielsen AT, Wu CY, Roseman S, Schoolnik GK. The Vibrio cholerae chitin utilization program. Proc Natl Acad Sci USA, 2004, 101(8): 2524-2529.
[16] Uchiyama T, Kaneko R, Yamaguchi J, Inoue A, Yanagida T, Nikaidou N, Regue M, Watanabe T. Uptake of N,N'-diacetylchitobiose
[(GlcNAc)2] via the phosphotransferase system is essential for chitinase production by Serratia marcescens 2170. J Bacteriol, 2003, 185(6): 1776-1782.
[17] Nelson DR, Rhodes RG, Atoyan JA. The chitobiose transporter, chbC, is required for chitin utilization in Borrelia burgdorferi. BMC Microbiol, 2010, 10: 21.
[18] Li XB, Roseman S. The chitinolytic cascade in Vibrios is regulated by chitin oligosaccharides and a two-component chitin catabolic sensor/kinase. Proc Natl Acad Sci USA
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