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荚膜组织胞浆菌中酵母相特异性基因产物在细胞壁的定位。

Localization of a yeast-phase-specific gene product to the cell wall in Histoplasma capsulatum.

作者信息

Weaver C H, Sheehan K C, Keath E J

机构信息

Department of Biology, Saint Louis University, Missouri 63103, USA.

出版信息

Infect Immun. 1996 Aug;64(8):3048-54. doi: 10.1128/iai.64.8.3048-3054.1996.

Abstract

A yeast-phase-specific gene, yps-3, has been identified in the virulent Histoplasma capsulatum strain, G217B. Although DNA sequencing of the genomic yps-3 gene from G217B failed to detect homologies with known proteins, the 5' end of a yps-3 cDNA contained a consensus signal sequence. A 519-bp fragment of the cDNA containing the translational stop codon was linker modified and inserted into the bacterial expression vector, pATH 1. Escherichia coli extracts containing the pATH 1 vector alone expressed a major 34-kDa TrpE polypeptide following induction with indoleacrylic acid, while the pATH 1/yps-3 construct produced a predominant 54-kDa TrpE/yps-3 fusion protein. Polyclonal rabbit sera directed against G217B reacted exclusively with the 54-kDa fusion protein in Western blots (immunoblots); serum samples from three patients with acute pulmonary or disseminated histoplasmosis were also positive. To localize the yps-3 protein within G217B, a monoclonal antibody (MAb 7.1) which recognized the yps-3 portion of the fusion protein was generated. A 17.4-kDa protein was detected with MAb 7.1 in Western blots prepared from cell wall fractions of G217B; cytoplasmic fractions were unreactive. No yps-3 antigen was detected in either fraction of the Downs strain, which fails to express the yps-3 gene. MAb 7.1 also detected a 17.4-kDa antigen in ethanol-precipitated culture supernatants derived from G217B. These findings localize the yps-3 gene product to the cell wall and culture supernatants, where the protein may influence the phase transition or the maintenance of the yeast state.

摘要

在强毒力的荚膜组织胞浆菌菌株G217B中鉴定出一个酵母相特异性基因yps - 3。尽管对G217B基因组yps - 3基因进行DNA测序未检测到与已知蛋白质的同源性,但yps - 3 cDNA的5'端含有一个共有信号序列。将包含翻译终止密码子的519 bp cDNA片段进行接头修饰后插入细菌表达载体pATH 1。单独含有pATH 1载体的大肠杆菌提取物在用吲哚丙烯酸诱导后表达一种主要的34 kDa色氨酸合成酶E(TrpE)多肽,而pATH 1/yps - 3构建体产生一种主要的54 kDa TrpE/yps - 3融合蛋白。针对G217B的兔多克隆血清在蛋白质免疫印迹(免疫印迹)中仅与54 kDa融合蛋白发生反应;三名急性肺型或播散型组织胞浆菌病患者的血清样本也呈阳性。为了在G217B中定位yps - 3蛋白,制备了一种识别融合蛋白yps - 3部分的单克隆抗体(MAb 7.1)。在用G217B细胞壁组分制备的蛋白质免疫印迹中,MAb 7.1检测到一种17.4 kDa的蛋白;细胞质组分无反应。在不表达yps - 3基因的唐斯菌株的任何一个组分中均未检测到yps - 3抗原。MAb 7.1在源自G217B的乙醇沉淀培养上清液中也检测到一种17.4 kDa的抗原。这些发现将yps - 3基因产物定位到细胞壁和培养上清液中,该蛋白可能在其中影响相变或酵母状态的维持。

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