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白色念珠菌的ARG4基因。

The ARG4 gene of Candida albicans.

作者信息

Hoyer L L, Magee B B, Rikkerink E H, Scherer S

机构信息

Human Genome Center, Lawrence Berkeley Laboratory, University of California, Berkeley 94720.

出版信息

Gene. 1994 May 16;142(2):213-8. doi: 10.1016/0378-1119(94)90263-1.

Abstract

The DNA sequence of a Candida albicans genomic fragment known to complement the arginine mutation designated arg57 in strain 1006 contains an ORF of 1404 nucleotides (nt) predicting a protein of 468 amino acids (aa). Database searches indicated that the deduced protein shares 75% identity and 85% similarity with the ARG4 protein of Saccharomyces cerevisiae. Analysis of the percent aa identity between C. albicans and S. cerevisiae sequences included in available databases suggested these values are within the range expected for biosynthetic enzymes from the two organisms which share similar function. Experiments to isolate C. albicans ARG4 by complementation in an arg4 strain of S. cerevisiae yielded a plasmid (pARG4-1) with a restriction map identical to that of the sequenced clone. From these data, we conclude that the gene previously designated ARG57 is in fact ARG4 encoding the enzyme argininosuccinate lyase (ASL). These results were unexpected, since ARG57 had been localized to chromosome 7, while a mutation causing an ASL deficiency had been linked to ade1, which is on chromosome R. Transformation of C. albicans strains with pARG4-1 indicated it complemented the arginine auxotrophy in strains TMSU221 and 1435, a derivative of 1006. Examination of commonly utilized C. albicans arginine auxotrophs by spheroplast fusion analysis indicated these strains comprise two complementation groups: one consisting of 1006 and TMSU221, which are arg4, and the other of A642, hOG318, hOG357, FC18-6 and WC-5-4, which possess an undefined defect in the arginine biosynthetic pathway which we designate arg100.

摘要

已知能互补1006菌株中精氨酸突变体(命名为arg57)的白色念珠菌基因组片段的DNA序列,包含一个1404个核苷酸(nt)的开放阅读框(ORF),预测编码一个468个氨基酸(aa)的蛋白质。数据库搜索表明,推导的蛋白质与酿酒酵母的ARG4蛋白有75%的同一性和85%的相似性。对现有数据库中白色念珠菌和酿酒酵母序列之间氨基酸同一性百分比的分析表明,这些值处于具有相似功能的两种生物体的生物合成酶预期的范围内。通过在酿酒酵母的arg4菌株中互补来分离白色念珠菌ARG4的实验,得到了一个质粒(pARG4 - 1),其限制性图谱与测序克隆的相同。根据这些数据,我们得出结论,先前命名为ARG57的基因实际上是编码精氨琥珀酸裂解酶(ASL)的ARG4。这些结果出乎意料,因为ARG57已定位到7号染色体,而导致ASL缺陷的突变已与位于R染色体上的ade1相关联。用pARG4 - 1转化白色念珠菌菌株表明,它能互补TMSU221和1435(1006的衍生物)菌株中的精氨酸营养缺陷型。通过原生质体融合分析对常用的白色念珠菌精氨酸营养缺陷型进行检测表明,这些菌株包括两个互补组:一组由1006和TMSU221组成,它们是arg4;另一组由A642、hOG318、hOG357、FC18 - 6和WC - 5 - 4组成,它们在精氨酸生物合成途径中存在未定义的缺陷,我们将其命名为arg100。

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