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Yeast peroxisomes: structure, functions and biotechnological opportunities

机译:酵母过氧化物酶体:结构,功能和生物技术机会

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Peroxisomes are ubiquitous organelles found in most eukaryotic cells. In yeasts, peroxisomes play important roles in cell metabolism, especially in different catabolic processes including fatty acid beta-oxidation, the glyoxylic shunt and methanol metabolism, as well as some biosynthetic processes. In addition, peroxisomes are the compartment in which oxidases and catalase are localized. New peroxisomes mainly arise by fission of pre-existing ones, although they can also be formed from the endoplasmic reticulum (ER). Peroxisomes consist of matrix-soluble proteins and membrane proteins known as peroxins. A total of 34 PEX peroxin genes and proteins have been identified to date. and their functions have been elucidated. Protein import into peroxisomes depends on peroxins and requires specific signals in the structure of transported proteins: PTS1, PTS2 and mPTS. The mechanisms of metabolite penetration into peroxisomes are still poorly understood. Peroxisome number and the volume occupied by these organelles are tightly regulated. Methanol, fatty acids and methylamine act as efficient peroxisome proliferators, whereas glucose and ethanol induce peroxisome autophagic degradation (pexophagy). To date, 42 Atg proteins involved in pexophagy are known. Catabolism and alcoholic fermentation of the major pentose sugar, xylose, depend on peroxisomal enzymes. Overexpression of peroxisomal transketolase and transaldolase activates xylose fermentation. Peroxisomes could be useful as target organelles for overexpression of foreign toxic proteins.
机译:过氧化物酶体是在大多数真核细胞中普遍存在的细胞器。在酵母中,过氧化物酶体在细胞代谢中起重要作用,尤其是在不同的分解代谢过程中,包括脂肪酸β-氧化,乙醛分流和甲醇代谢以及某些生物合成过程。另外,过氧化物酶体是氧化酶和过氧化氢酶位于其中的区室。新的过氧化物酶体主要是由先存的过氧化物酶体裂变产生的,尽管它们也可以由内质网(ER)形成。过氧化物酶体由可溶于基质的蛋白质和称为过氧化物酶的膜蛋白组成。迄今为止,已经鉴定出总共34种PEX过氧化物酶基因和蛋白质。其功能已阐明。蛋白质输入到过氧化物酶体中取决于过氧化物酶,并且在转运蛋白的结构中需要特定的信号:PTS1,PTS2和mPTS。代谢物渗透到过氧化物酶体中的机制仍知之甚少。这些细胞器的过氧化物酶数和占据的体积受到严格调节。甲醇,脂肪酸和甲胺可作为有效的过氧化物酶体增殖物,而葡萄糖和乙醇则诱导过氧化物酶体自噬降解(有咽)。迄今为止,已知有42种Atg蛋白参与了排毒。主要戊糖(木糖)的分解代谢和酒精发酵取决于过氧化物酶体酶。过氧化物酶体转酮酶和反式醛缩酶的过表达激活木糖发酵。过氧化物酶体可用作过量表达外源毒性蛋白的靶细胞器。

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