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黄曲霉多聚半乳糖醛酸酶基因(pecA和pecB)的分离与鉴定

Isolation and characterization of polygalacturonase genes (pecA and pecB) from Aspergillus flavus.

作者信息

Whitehead M P, Shieh M T, Cleveland T E, Cary J W, Dean R A

机构信息

Department of Plant Pathology and Physiology, Clemson University, South Carolina 29634-0377, USA.

出版信息

Appl Environ Microbiol. 1995 Sep;61(9):3316-22. doi: 10.1128/aem.61.9.3316-3322.1995.

Abstract

Two genes, pecA and pecB, encoding endopolyglacturonases were cloned from a highly aggressive strain of Aspergillus flavus. The pecA gene consisted of 1,228 bp encoding a protein of 363 amino acids with a predicted molecular mass of 37.6 kDa, interrupted by two introns of 58 and 81 bp in length. Accumulation of pecA mRNA in both pectin- or glucose-grown mycelia in the highly aggressive strain matched the activity profile of a pectinase previously identified as P2c. Transformants of a weakly aggressive strain containing a functional copy of the pecA gene produced P2c in vitro, confirming that pecA encodes P2c. The coding region of pecB was determined to be 1,217 bp in length interrupted by two introns of 65 and 54 bp in length. The predicted protein of 366 amino acids had an estimated molecular mass of 38 kDa. Transcripts of this gene accumulated in mycelia grown in medium containing pectin alone, never in mycelia grown in glucose-containing medium, for both highly and weakly aggressive strains. Thus, pecB encodes the activity previously identified as P1 or P3. pecA and pecB share a high degree of sequence identity with polygalacturonase genes from Aspergillus parasiticus and Aspergillus oryzae, further establishing the close relationships between members of the A. flavus group. Conservation of intron positions in these genes also indicates that they share a common ancestor with genes encoding endopolyglacturonases of Aspergillus niger.

摘要

从一株高致病性黄曲霉菌株中克隆出了两个编码内切多聚半乳糖醛酸酶的基因,pecA和pecB。pecA基因由1228个碱基对组成,编码一个含363个氨基酸的蛋白质,预测分子量为37.6 kDa,该基因被两个长度分别为58和81个碱基对的内含子打断。在高致病性菌株中,果胶或葡萄糖培养的菌丝体中pecA mRNA的积累与先前鉴定为P2c的果胶酶活性谱相匹配。含有pecA基因功能拷贝的弱致病性菌株的转化体在体外产生了P2c,证实pecA编码P2c。pecB的编码区长度为1217个碱基对,被两个长度分别为65和54个碱基对的内含子打断。预测的含366个氨基酸的蛋白质估计分子量为38 kDa。对于高致病性和弱致病性菌株,该基因的转录本仅在单独含有果胶的培养基中生长的菌丝体中积累,而在含有葡萄糖的培养基中生长的菌丝体中从未积累。因此,pecB编码先前鉴定为P1或P3的活性。pecA和pecB与寄生曲霉和米曲霉的多聚半乳糖醛酸酶基因具有高度的序列同一性,进一步确立了黄曲霉组各成员之间的密切关系。这些基因内含子位置的保守性也表明它们与黑曲霉编码内切多聚半乳糖醛酸酶的基因有共同的祖先。

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