|本期目录/Table of Contents|

[1]张银波,江木兰,万霞,等.环境基因组DNA脂肪酶基因克隆与分析[J].应用与环境生物学报,2010,16(02):269-273.[doi:10.3724/SP.J.1145.2010.00269]
 ZHANG Yinbo,JIANG Mulan,WAN Xia,et al.Cloning and Analysis of a Lipase Gene from Environmental Genome DNA[J].Chinese Journal of Applied & Environmental Biology,2010,16(02):269-273.[doi:10.3724/SP.J.1145.2010.00269]
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环境基因组DNA脂肪酶基因克隆与分析()
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《应用与环境生物学报》[ISSN:1006-687X/CN:51-1482/Q]

卷:
16卷
期数:
2010年02期
页码:
269-273
栏目:
研究论文
出版日期:
2010-04-25

文章信息/Info

Title:
Cloning and Analysis of a Lipase Gene from Environmental Genome DNA
文章编号:
200903052
作者:
张银波江木兰万霞王汉中
(中国农业科学院油料作物研究所,农业部油料作物生物学重点开放实验室 武汉 430062)
Author(s):
ZHANG YinboJIANG MulanWAN XiaWANG Hanzhong
(Key Laboratory of Oil Crops Biology, Ministry of Agriculture, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China)
关键词:
环境基因组脂肪酶简并PCR毕赤酵母
Keywords:
environmental genome lipase degenerate PCR Pichia pastoris
分类号:
Q78 : Q936.561
DOI:
10.3724/SP.J.1145.2010.00269
文献标志码:
A
摘要:
为了建立从环境基因组DNA中直接克隆脂肪酶基因的通用方法,抽提餐馆灶台油污的环境基因组DNA,采用简并PCR等分子技术从中克隆到脂肪酶基因lip42及其对应的全长cDNA. 序列分析表明该基因的cDNA编码区序列全长为1 692 bp,编码1段由19个氨基酸残基组成的信号肽和1段由544个氨基酸残基组成的成熟肽,计算相对分子质量为61 541.51,其中含有强碱性氨基酸残基42个,强酸性氨基酸残基56个,等电点pI为5.428,有2个可能的N-糖基化位点. BLAST比对分析表明该序列与已发表的白地霉(Geotrichum geotrichum)脂肪酶基因(U02541)在核苷酸水平的一致性为99%. 该基因序列提交GenBank,登录号为DQ313172. 将该脂肪酶基因的开放阅读框克隆到毕赤酵母表达载体,转化毕赤酵母GS115,经罗丹明B平板功能筛选得到具脂肪酶活性的重组毕赤酵母菌株[GS115(pAMB768)],验证了直接从环境基因组DNA克隆脂肪酶基因的有效性. 图3 表1 参27
Abstract:
A lipase gene was cloned by degenerate PCR from environmental genome DNA extracted from the oil dirt on the hearth of a restaurant and designated as lip42. Its sequence was submitted to GenBank with the accession number of DQ313172 obtained. The cDNA of the putative lipase gene (lip42) consisted of 1 692 bp, including an open reading frame encoding a 19-amino acid signal peptide at the N-terminal end and a 544-amino acid mature protein with a predicted molecular mass of 61 541.51, with pI value of 5.482 and 2 potential N-glycosylation sites (N-X-T/S). The open reading frame was transformed into Pichia pastoris strain GS115 under the control of the AOX1 promoter by using vector pHBM906. Secretion expression of lip42 was detected from P. pastoris recombinant strain [GS115 (pAMB768)]. Fig 3, Tab 1, Ref 27

参考文献/References:

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备注/Memo

备注/Memo:
国家“863”项目(No. 2007AA100703)与国家公益性科研院所专项资金课题(No. 200703-19)资助 Supported by the National High-tech R & D Project of China (No. 2007AA100703) and the National Special Funds for Public Research Institutions of China (No. 200703-19)
更新日期/Last Update: 2010-04-20