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构巢曲霉中奎尼酸利用基因簇的三个酶结构基因QUTB、QUTC和QUTE的克隆与特性分析

Cloning and characterization of the three enzyme structural genes QUTB, QUTC and QUTE from the quinic acid utilization gene cluster in Aspergillus nidulans.

作者信息

Hawkins A R, Francisco Da Silva A J, Roberts C F

机构信息

Department of Biochemistry, School of Biological Sciences, University of Leicester, Leicester, UK.

出版信息

Curr Genet. 1985;9(4):305-11. doi: 10.1007/BF00419960.

Abstract

Heterologous DNA probes from the quinic acid gene cluster (QA) in Neurospora crassa (Schweizer 1981) have been used to isolate the corresponding gene cluster (QUT) from Aspergillus nidulans cloned in a phage lambda vector. N. crassa probes for each of the three enzyme structural genes in the cluster have been used to identify the corresponding genes within the A. nidulans cloned DNA. The three genes are in the same relative sequence [dehydrogenase (1), QA-3 = QUTB; dehydratase (3), QA-4 = QUTC; dehydroquinase (2), QA-2 = QUTE] though contained within a 3.4 kb DNA sequence in Aspergillus compared to a 5.4 kb sequence in Neurospora. The A. nidulans dehydroquinase (2) gene QUTE has been shown to complement an auxotrophic mutant aroD6 of Escherichia coli lacking biosynthetic dehydroquinase when tested for growth at 30 degrees C. A mutant of A. nidulans lacking catabolic dehydroquinase (2) and designated qutE208 has been isolated and shown to be tightly linked to the gene cluster, which maps between the ornB and fwA loci in linkage group VIII.

摘要

来自粗糙脉孢菌(Schweizer,1981)奎尼酸基因簇(QA)的异源DNA探针已被用于从克隆于噬菌体λ载体中的构巢曲霉中分离相应的基因簇(QUT)。该基因簇中三个酶结构基因各自对应的粗糙脉孢菌探针已被用于在构巢曲霉克隆DNA中鉴定相应的基因。这三个基因具有相同的相对序列[脱氢酶(1),QA - 3 = QUTB;脱水酶(3),QA - 4 = QUTC;脱氢奎尼酸酶(2),QA - 2 = QUTE],不过在构巢曲霉中它们包含在一个3.4 kb的DNA序列中,而在粗糙脉孢菌中为一个5.4 kb的序列。当在30℃下测试生长情况时,构巢曲霉脱氢奎尼酸酶(2)基因QUTE已被证明可互补缺乏生物合成脱氢奎尼酸酶的大肠杆菌营养缺陷型突变体aroD6。已分离出一个缺乏分解代谢脱氢奎尼酸酶(2)且命名为qutE208的构巢曲霉突变体,并证明它与基因簇紧密连锁,该基因簇定位于连锁群VIII中的ornB和fwA基因座之间。

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