Microbiome of Fungus-Growing Termites: a New Reservoir for Lignocellulase Genes

被引:52
作者
Liu, Ning [1 ]
Yan, Xing [2 ]
Zhang, Meiling [3 ]
Xie, Lei [1 ]
Wang, Qian [1 ]
Huang, Yongping [1 ]
Zhou, Xuguo [4 ]
Wang, Shengyue [5 ]
Zhou, Zhihua [2 ]
机构
[1] Chinese Acad Sci, Key Lab Insect Dev & Evolutionary Biol, Inst Plant Physiol & Ecol, Shanghai Inst Biol Sci, Shanghai 200032, Peoples R China
[2] Chinese Acad Sci, Key Lab Synthet Biol, Inst Plant Physiol & Ecol, Shanghai Inst Biol Sci, Shanghai 200032, Peoples R China
[3] E China Normal Univ, Dept Biochem & Mol Biol, Coll Life Sci, Shanghai 200062, Peoples R China
[4] Univ Kentucky, Dept Entomol, Lexington, KY 40546 USA
[5] Chinese Natl Human Genome Ctr, Shanghai 201203, Peoples R China
基金
国家高技术研究发展计划(863计划); 上海市自然科学基金; 中国国家自然科学基金;
关键词
MULTIPLE DISPLACEMENT AMPLIFICATION; UNCULTURED MICROORGANISMS; MACROTERMES-BELLICOSUS; ENVIRONMENTAL DNA; XYLANASES; METAGENOMICS; EXPRESSION; CELLULASE; SEQUENCES; ENZYMES;
D O I
10.1128/AEM.01521-10
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Fungus-growing termites play an important role in lignocellulose degradation and carbon mineralization in tropical and subtropical regions, but the degradation potentiality of their gut microbiota has long been neglected. The high quality and quantity of intestinal microbial DNA are indispensable for exploring new cellulose genes from termites by function-based screening. Here, using a refined intestinal microbial DNA extraction method followed by multiple-displacement amplification (MDA), a fosmid library was constructed from the total microbial DNA isolated from the gut of a termite growing in fungi. Functional screening for endoglucanase, cellobiohydrolase, beta-glucosidase, and xylanase resulted in 12 beta-glucosidase-positive clones and one xylanase-positive clone. The sequencing result of the xylanase-positive clone revealed an 1,818-bp open reading frame (ORF) encoding a 64.5-kDa multidomain endo-1,4-beta-xylanase, designated Xyl6E7, which consisted of an N-terminal GH11 family catalytic domain, a CBM_4_9 domain, and a Listeria-Bacteroides repeat domain. Xyl6E7 was a highly active, substrate-specific, and endo-acting alkaline xylanase with considerably wide pH tolerance and stability but extremely low thermostability.
引用
收藏
页码:48 / 56
页数:9
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