首页|捕食线虫真菌Drechslerella dactyloides Gα基因克隆及系统发育分析

捕食线虫真菌Drechslerella dactyloides Gα基因克隆及系统发育分析

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运用简并PCR和DNA Walking技术首次从捕食线虫真菌(Drechslerella dactyloides)中克隆了Gα的编码全长基因Dgal.该基因全长1 420 bp,编码356个氨基酸,推测其编码蛋白的分子质量和pI值分别为40.84ku和6.68.通过同源比对和系统发育分析,表明Dgal属于真菌Gα的第3类群,推测Dgal具有激活腺苷酸环化酶的作用.
Gene cloning and phylogenetic analysis on the Gα from nematode trapping fungus Drechslerella dactyloides
Dgal,a gene encoding Got,was firstly cloned from nematode - trapping fungus Drechslerella dac-tyloides by using methods of degenerate PCR and DNA Walking. The Dgal comprised 1 402 base pairs in length, and encoded a polypeptide with 356 amino acid residues. The theoretic molecular mass and pl of Dgal are deduced as 40. 84 ku and 6.68,respectively. A phylogenetic analysis on fungal Got indicates that the Dgal belongs to group Ⅲ of fungal Got, which possibly has the function as stimulating the adenylyl cyclases.

张晟、乔敏、马莉、林碧莲、辛雄、莫明和

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云南大学,生物资源保护与利用重点实验室,云南,昆明,650091

捕食线虫真菌 基因克隆 Drechslerella dactyloides

国家自然科学基金云南省应用基础研究面上项目

307600022007C014M

2011

云南大学学报(自然科学版)
云南大学

云南大学学报(自然科学版)

CSTPCDCSCD北大核心
影响因子:0.663
ISSN:0258-7971
年,卷(期):2011.33(1)
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