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ALG2,即多形汉逊酵母异柠檬酸裂解酶基因。

ALG2, the Hansenula polymorpha isocitrate lyase gene.

作者信息

Berardi Enrico, Gambini Annalisa, Bellu Anna Rita

机构信息

Laboratorio di Genetica Microbica, Dipartimento di Biotecnologie, Università Politecnica delle Marche, Via Brecce Bianche, 60131 Ancona, Italy.

出版信息

Yeast. 2003 Jul 15;20(9):803-11. doi: 10.1002/yea.1002.

Abstract

To set the basis for molecular and cellular studies of the glyoxylate cycle in methylotrophic yeasts, we isolated and characterized ALG2, the Hansenula polymorpha isocitrate lyase gene. Complementation work and sequence analysis revealed an ORF of 1458 nucleotides, encoding a 486 amino acid protein with a predicted molecular mass of 54.9 kDa. This protein is shorter than the Saccharomyces cerevisiae and Candida tropicalis ICLs, lacks a PST1 signal and possesses a PTS2-like signal. The transcriptional regulation of ALG2 mRNA levels by carbon source is mainly achieved by glucose repression-derepression, whereas ethanol induction plays only a minor role. We present evidence indicating that, in H. polymorpha, neither isocitrate lyase activity nor the ALG2 gene product are necessary for C(1)-peroxisome degradation triggered by ethanol. Therefore, the involvement of glyoxylate in degradation, as described by Kulachkovsky et al. (1997) for Pichia methanolica, does not necessarily apply to all methylotrophic yeasts. The relevant nucleotide sequence has been deposited at GenBank (Accession No. AF373067.1).

摘要

为了奠定甲基营养型酵母中乙醛酸循环的分子和细胞研究基础,我们分离并鉴定了多形汉逊酵母异柠檬酸裂解酶基因ALG2。互补实验和序列分析揭示了一个1458个核苷酸的开放阅读框,编码一个486个氨基酸的蛋白质,预测分子量为54.9 kDa。该蛋白质比酿酒酵母和热带假丝酵母的异柠檬酸裂解酶短,缺乏PST1信号并具有类似PTS2的信号。碳源对ALG2 mRNA水平的转录调控主要通过葡萄糖阻遏-去阻遏实现,而乙醇诱导作用较小。我们提供的证据表明,在多形汉逊酵母中,乙醇引发的C(1)-过氧化物酶体降解既不需要异柠檬酸裂解酶活性,也不需要ALG2基因产物。因此,如Kulachkovsky等人(1997年)对甲醇毕赤酵母所描述的,乙醛酸参与降解的情况不一定适用于所有甲基营养型酵母。相关核苷酸序列已存入GenBank(登录号AF373067.1)。

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