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白色念珠菌肽转运基因的克隆

Cloning of a Candida albicans peptide transport gene.

作者信息

Basrai Munira A, Lubkowitz Mark A, Perry Jack R, Miller David, Krainer Eduardo, Naider Fred, Becker Jeffrey M

机构信息

Department of Microbiology and Program in Cellular, Molecular, and Developmental Biology, University of Tennessee, Knoxville, TN 37996-0845, USA.

Department of Chemistry, College of Staten Island, City University of New York, Staten Island, New York 10301, USA.

出版信息

Microbiology (Reading). 1995 May;141 ( Pt 5):1147-1156. doi: 10.1099/13500872-141-5-1147.

Abstract

A Candida albicans peptide transport gene, CaPTR2, was cloned from a C. albicans genomic library by functional complementation of a peptide transport deficient mutant (strain ptr2-2) of Saccharomyces cerevisiae. CaPTR2 restored peptide transport to transformants as determined by uptake of radiolabelled dileucine, growth on dipeptides as sources of required amino acids, and restoration of growth inhibition by toxic peptides. Plasmid curing experiments demonstrated that the peptide transport phenotype was plasmid borne. CaPTR2 was localized to chromosome R of C. albicans by contour-clamped homologous electric field gel chromosome blots. Deletion subclones and frameshift mutagenesis were used to narrow the peptide transport complementing region to a 5.1 kb DNA fragment. DNA sequencing of the complementing region identified an ORF of 1869 bp containing an 84 nucleotide intron. The deduced amino acid sequence predicts a protein of 70 kDa consisting of 623 amino acids with 12 hydrophobic segments. A high level of identity was found between the predicted protein and peptide transport proteins of S. cerevisiae and Arabidopsis thaliana. This study represents the first steps in the genetic characterization of peptide transport in C. albicans and initiates a molecular approach for the study of drug delivery against this pathogen.

摘要

通过对酿酒酵母的肽转运缺陷突变体(菌株ptr2-2)进行功能互补,从白色念珠菌基因组文库中克隆出一个白色念珠菌肽转运基因CaPTR2。通过放射性标记的双亮氨酸摄取、以二肽作为必需氨基酸来源的生长情况以及有毒肽对生长抑制的恢复情况来确定,CaPTR2可恢复转化体的肽转运能力。质粒消除实验表明,肽转运表型由质粒携带。通过轮廓钳制同源电场凝胶染色体印迹法,将CaPTR2定位到白色念珠菌的R染色体上。利用缺失亚克隆和移码诱变将肽转运互补区域缩小到一个5.1 kb的DNA片段。对互补区域进行DNA测序,鉴定出一个1869 bp的开放阅读框,其中包含一个84个核苷酸的内含子。推导的氨基酸序列预测出一个70 kDa的蛋白质,由623个氨基酸组成,有12个疏水片段。在预测的蛋白质与酿酒酵母和拟南芥的肽转运蛋白之间发现了高度的同源性。这项研究代表了白色念珠菌肽转运遗传特征研究的第一步,并开启了针对这种病原体进行药物递送研究的分子方法。

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