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酿酒酵母和异常汉逊酵母原生质球包膜的结构与化学成分

Structure and chemical composition of prospheroplast envelopes of Saccharomyces cerevisiae and Hansenula anomala.

作者信息

Darling S, Theilade J, Birch-Andersen A

出版信息

J Bacteriol. 1972 Apr;110(1):336-45. doi: 10.1128/jb.110.1.336-345.1972.

DOI:10.1128/jb.110.1.336-345.1972
PMID:4552997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC247416/
Abstract

Cells of Saccharomyces cerevisiae and Hansenula anomala were digested with snail enzyme under conditions yielding prospheroplasts. Surrounding envelopes were isolated after lysis of prospheroplasts in distilled water. The envelope material was embedded and sectioned for electron microscopy, and thin, hollow structures still retaining the elongated form of the original cells were seen. The envelopes were of low electron density in sections stained with uranyl magnesium acetate and lead citrate, but were more electron-dense when stained with phosphotungstic acid. Shadowed preparations of prospheroplast envelopes revealed structures resembling ghosts. These "ghosts" were similar to the original cells in form and size but seemed to be very thin. Varying numbers of anular structures (bud scars) were found on them. Chemical analyses of the envelope indicated that an alkali-soluble glucan was a major constituent. The results show that the prospheroplast envelope is part of the original cell wall of the yeast and is located in close apposition to the cytoplasmic membrane.

摘要

在能产生原生质球的条件下,用蜗牛酶消化酿酒酵母和异常汉逊酵母的细胞。原生质球在蒸馏水中裂解后,分离出其周围的包膜。将包膜材料包埋并切片用于电子显微镜观察,可见仍保留原始细胞细长形态的薄而中空的结构。在用醋酸铀镁和柠檬酸铅染色的切片中,包膜的电子密度较低,但在用磷钨酸染色时,电子密度更高。原生质球包膜的投影制备显示出类似幽灵的结构。这些“幽灵”在形态和大小上与原始细胞相似,但似乎非常薄。在它们上面发现了数量不等的环状结构(芽痕)。对包膜的化学分析表明,一种碱溶性葡聚糖是主要成分。结果表明,原生质球包膜是酵母原始细胞壁的一部分,与细胞质膜紧密相邻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/e19579e96d9d/jbacter00360-0361-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/1479bf4de834/jbacter00360-0356-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/8f298883ffc7/jbacter00360-0356-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/3e20d92137b0/jbacter00360-0357-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/8175db6a0102/jbacter00360-0358-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/c2a9c55aad56/jbacter00360-0359-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/2471e91f06f2/jbacter00360-0360-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/e19579e96d9d/jbacter00360-0361-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/1479bf4de834/jbacter00360-0356-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/8f298883ffc7/jbacter00360-0356-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/3e20d92137b0/jbacter00360-0357-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/8175db6a0102/jbacter00360-0358-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/c2a9c55aad56/jbacter00360-0359-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/2471e91f06f2/jbacter00360-0360-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0598/247416/e19579e96d9d/jbacter00360-0361-a.jpg

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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A ROUTINE TECHNIQUE FOR DOUBLE-STAINING ULTRATHIN SECTIONS USING URANYL AND LEAD SALTS.一种使用铀盐和铅盐对超薄切片进行双重染色的常规技术。
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The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.在电子显微镜检查中,将高pH值的柠檬酸铅用作电子不透明染色剂。
J Cell Biol. 1963 Apr;17(1):208-12. doi: 10.1083/jcb.17.1.208.
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Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.细胞化学与电子显微镜术。醛类固定对细胞超微结构及酶活性的保存作用。
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[Electron microscopic study on plasmas containing desoxyribonucleic acid. I. Nucleoids of actively growing bacteria].[含脱氧核糖核酸血浆的电子显微镜研究。I. 活跃生长细菌的拟核]
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An alkali-soluble glucan fraction from the cell walls of the yeast Saccharomyces carlsbergensis.来自卡尔斯伯酵母细胞壁的一种碱溶性葡聚糖组分。
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Do yeasts form true protoplasts?酵母会形成真正的原生质体吗?
C R Trav Lab Carlsberg. 1966;35(15):363-8.
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