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酿酒酵母中编码二腺苷5',5'''-P1,P4-四磷酸(Ap4A)磷酸化酶的基因的测序及增强表达。

Sequencing and enhanced expression of the gene encoding diadenosine 5',5'''-P1, P4-tetraphosphate (Ap4A) phosphorylase in Saccharomyces cerevisiae.

作者信息

Kaushal V, Avila D M, Hardies S C, Barnes L D

机构信息

Department of Biochemistry, University of Texas Health Science Center, San Antonio 78284-7760.

出版信息

Gene. 1990 Oct 30;95(1):79-84. doi: 10.1016/0378-1119(90)90416-o.

Abstract

The gene, DTP, coding for diadenosine 5',5'''-P1, P4-tetraphosphate (Ap4A) phosphorylase was isolated from a Saccharomyces cerevisiae genomic DNA library in lambda gt11. In yeast and Escherichia coli transformed with the multicopy vector, YEp352, containing the cloned DTP gene, the Ap4A phosphorylase was produced at levels nine- to 17-fold higher than in untransformed hosts. The nucleotide (nt) sequence was determined. The gene codes for a polypeptide chain of 321 amino acids (aa). Two-aa sequence motifs of possible significance were identified: a potential adenine nt binding site and a potential phosphorylation site. The DTP gene is located on yeast chromosome III and is present as a single copy. Although multicopy vector expression increased the Ap4A phosphorylase activity ninefold above the endogenous activity in transformed yeast, the intracellular concentration of Ap4A did not decrease and the growth rate of the yeast was unchanged.

摘要

从λgt11载体中的酿酒酵母基因组DNA文库中分离出编码二腺苷5′,5″-P1,P4-四磷酸(Ap4A)磷酸化酶的基因DTP。在用含有克隆的DTP基因的多拷贝载体YEp352转化的酵母和大肠杆菌中,Ap4A磷酸化酶的产生水平比未转化宿主高9至17倍。测定了核苷酸(nt)序列。该基因编码一条由321个氨基酸(aa)组成的多肽链。鉴定出了两个可能具有重要意义的双氨基酸序列基序:一个潜在的腺嘌呤nt结合位点和一个潜在的磷酸化位点。DTP基因位于酵母的III号染色体上,且以单拷贝形式存在。尽管多拷贝载体表达使转化酵母中的Ap4A磷酸化酶活性比内源活性提高了9倍,但Ap4A的细胞内浓度并未降低,酵母的生长速率也未改变。

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