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寄生曲霉新型多聚半乳糖醛酸酶编码基因的克隆与特性分析

Cloning and characterization of a novel polygalacturonase-encoding gene from Aspergillus parasiticus.

作者信息

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

机构信息

USDA-ARS, Southern Regional Research Center, New Orleans, LA 70179.

出版信息

Gene. 1995 Feb 3;153(1):129-33. doi: 10.1016/0378-1119(94)00749-i.

Abstract

Pectinases produced by Aspergillus flavus and A. parasiticus are believed to play a significant role in the ability of these fungi to spread in cotton bolls and other crops. Utilizing a DNA probe, generated by PCR, of the Aspergillus niger pgaII gene, we have isolated a novel, constitutively expressed polygalacturonase (PG)-encoding gene (pecA) from an A. parasiticus cDNA library. DNA sequence analysis and the deduced amino acid (aa) sequence of pecA demonstrated significant identity at the nucleotide and aa levels with other PG of fungal origin. Northern blot analysis of RNA isolated from A. parasiticus grown on either glucose or pectin as the sole carbon source showed that pecA was expressed during growth in both media.

摘要

黄曲霉和寄生曲霉产生的果胶酶被认为在这些真菌在棉铃和其他作物中传播的能力方面发挥着重要作用。利用通过PCR产生的黑曲霉pgaII基因的DNA探针,我们从寄生曲霉cDNA文库中分离出一个新的、组成型表达的多聚半乳糖醛酸酶(PG)编码基因(pecA)。pecA的DNA序列分析和推导的氨基酸(aa)序列在核苷酸和氨基酸水平上与其他真菌来源的PG显示出显著的同一性。对以葡萄糖或果胶作为唯一碳源生长的寄生曲霉分离的RNA进行Northern印迹分析表明,pecA在两种培养基生长期间均有表达。

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