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UGD1, Encoding the Cryptococcus neoformans UDP-Glucose Dehydrogenase, Is Essential for Growth at 37°C and for Capsule Biosynthesis

机译:UGD1,编码新型隐球菌UDP-葡萄糖脱氢酶,对于37°C的生长和胶囊的生物合成至关重要

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We report the identification and disruption of the Cryptococcus neoformans var. grubii UGD1 gene encoding the UDP-glucose dehydrogenase, which catalyzes the conversion of UDP-glucose into UDP-glucuronic acid. Deletion of UGD1 led to modifications in the cell wall, as revealed by changes in the sensitivity of ugd1Δ cells to sodium dodecyl sulfate, NaCl, and sorbitol. Moreover, two of the yeast's major virulence factors—capsule biosynthesis and the ability to grow at 37°C—were impaired in ugd1Δ strains. These results suggest that the UDP-dehydrogenase represents the major, and maybe only, biosynthetic pathway for UDP-glucuronic acid in C. neoformans. Consequently, deletion of UGD1 blocked not only the synthesis of UDP-glucuronic acid but also that of UDP-xylose. To differentiate the phenotype(s) associated with the UDP-glucuronic acid defect alone from those linked to the UDP-xylose defect, ugd1Δ mutants were phenotypically compared to strains from which the gene encoding UDP-xylose synthase (i.e., that required for synthesis of UDP-xylose) had been deleted. Finally, studies of strains from which one of the four CAP genes (CAP10, CAP59, CAP60, or CAP64) had been deleted revealed common cell wall phenotypes associated with the acapsular state.
机译:我们报告了新隐球菌 var的鉴定和破坏。 grubii UGD1 基因编码UDP-葡萄糖脱氢酶,可催化UDP-葡萄糖转化为UDP-葡萄糖醛酸。 UGD1 的缺失导致细胞壁发生修饰,这由 ugd1 Δ细胞对十二烷基硫酸钠,NaCl和山梨醇的敏感性变化所揭示。此外, ugd1 Δ菌株损害了酵母的两个主要毒力因子,即胶囊的生物合成和在37°C下的生长能力。这些结果表明,UDP-脱氢酶代表了 C中UDP-葡萄糖醛酸的主要(也许仅是)生物合成途径。新甲虫。因此, UGD1 的缺失不仅阻止了UDP-葡萄糖醛酸的合成,而且阻止了UDP-木糖的合成。为了区分仅与UDP-葡萄糖醛酸缺陷相关的表型与与UDP-木糖缺陷相关的表型,将 ugd1 Δ突变体在表型上与菌株中编码UDP-木糖合酶的基因进行了比较。 (即合成UDP-木糖所需的)(已删除)。最后,研究了四个 CAP 基因( CAP10 CAP59 CAP60 或< em> CAP64 )已被删除,揭示了与荚膜状态相关的常见细胞壁表型。

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