首页> 外文期刊>Journal of Electron Microscopy >Scanning and negative-staining electron microscopy of protoplast regeneration of a wild-type and two chitin synthase mutants in the pathogenic yeast Candida glabrata
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Scanning and negative-staining electron microscopy of protoplast regeneration of a wild-type and two chitin synthase mutants in the pathogenic yeast Candida glabrata

机译:病原酵母光滑念珠菌中野生型和两个几丁质合酶突变体原生质体再生的扫描和负染色电子显微镜

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摘要

Protoplast regeneration of a wild-type and two mutant strains of Candida glabrata defective in CHS3 homologues encoding class IV chitin synthase in Saccharomyces cerevisiae was examined by scanning and negative-staining electron microscopy. In the wild-type strain, small particles and short filaments appeared on the protoplast surface at 10 min, filamentous materials covered the entire surface of the protoplast at 1 h, granular materials started filling interspaces of filamentous materials at 2 h and regeneration was completed at 6 h. The filamentous materials consisted of microfibrils of various widths ranging from ≤5 to 40 nm, and composed of β-glucan. Protoplasts of the two chitin synthase mutant strains of Δchs3A and Δchs3B completed regeneration essentially by the same process as wild-type strain, although it took more time. These results suggest that CHS3A and CHS3B genes may have important roles in cell wall formation during protoplast regeneration, but can be compensated by other cell wall enzymes.
机译:通过扫描和负染色电子显微镜检查了酿酒酵母中编码IV类几丁质合酶的CHS3同源物中有缺陷的野生型和两种光滑念珠菌菌株的原生质体再生。在野生型菌株中,原生质体表面在10分钟时出现小颗粒和短丝,在1 h时丝状物质覆盖了原生质体的整个表面,在2 h粒状物质开始填充丝状物质的空隙,并在2 h完成再生。 6小时丝状材料由宽度范围≤5至40 nm的微纤维组成,并由β-葡聚糖组成。 Δchs3A和Δchs3B的两个几丁质合酶突变菌株的原生质体通过与野生型菌株相同的过程完成了再生,尽管花费了更多时间。这些结果表明CHS3A和CHS3B基因可能在原生质体再生过程中在细胞壁形成中起重要作用,但可以被其他细胞壁酶所补偿。

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