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正构烷烃培养的麦芽糖假丝酵母中主要微粒体蛋白可翻译mRNA的增加。

Increase of translatable mRNA for major microsomal proteins in n-alkane-grown Candida maltosa.

作者信息

Sunairi M, Watabe K, Takagi M, Yano K

出版信息

J Bacteriol. 1984 Dec;160(3):1037-40. doi: 10.1128/jb.160.3.1037-1040.1984.

DOI:10.1128/jb.160.3.1037-1040.1984
PMID:6501225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC215815/
Abstract

In an n-alkane-assimilating Candida sp., transfer from glucose- to n-alkane-containing medium induced changes in the microsomal proteins, and several distinctive polypeptides were demonstrated in the solubilized microsomal fraction derived from n-alkane-grown cells. Long-term-labeling and pulse-labeling experiments in vivo demonstrated the synthesis of the specific microsomal polypeptides. The polypeptides were synthesized as in vitro translation products directed by polyadenylated RNA extracted from n-alkane-grown cells. Two major polypeptides were partially purified from the microsomal fraction from n-alkane-grown cells, and antiserum was prepared in a rabbit. Immunoprecipitation of these two polypeptides was accompanied by an increase in the amount of translatable mRNA. The molecular weights of the polypeptides derived from long-term-labeling, pulse-labeling and in vitro translation experiments appeared to be identical.

摘要

在一株同化正构烷烃的假丝酵母中,从含葡萄糖的培养基转移至含正构烷烃的培养基会引起微粒体蛋白的变化,并且在源自正构烷烃培养细胞的溶解微粒体部分中证实了几种独特的多肽。体内长期标记和脉冲标记实验证明了特定微粒体多肽的合成。这些多肽是由从正构烷烃培养细胞中提取的聚腺苷酸化RNA作为体外翻译产物合成的。从正构烷烃培养细胞的微粒体部分中部分纯化了两种主要多肽,并在兔中制备了抗血清。这两种多肽的免疫沉淀伴随着可翻译mRNA量的增加。长期标记、脉冲标记和体外翻译实验得到的多肽的分子量似乎是相同的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/d90823d64dcb/jbacter00229-0217-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/9a4db1afd1c1/jbacter00229-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/3bc03a9e016d/jbacter00229-0216-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/d90823d64dcb/jbacter00229-0217-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/9a4db1afd1c1/jbacter00229-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/3bc03a9e016d/jbacter00229-0216-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aff/215815/d90823d64dcb/jbacter00229-0217-a.jpg

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本文引用的文献

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Eur J Biochem. 1982 Dec 15;129(2):251-5. doi: 10.1111/j.1432-1033.1982.tb07046.x.
2
Synthesis in vitro of precursor-type carnitine acetyltransferase with messenger RNA from Candida tropicalis.利用热带假丝酵母的信使核糖核酸体外合成前体型肉碱乙酰转移酶
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Control of intracellular protein traffic.细胞内蛋白质运输的调控
通过使用从麦芽糖假丝酵母基因组中分离出的自主复制序列(ARS)位点构建麦芽糖假丝酵母宿主-载体系统。
J Bacteriol. 1986 Aug;167(2):551-5. doi: 10.1128/jb.167.2.551-555.1986.
4
Nucleotide sequencing analysis of a LEU gene of Candida maltosa which complements leuB mutation of Escherichia coli and leu2 mutation of Saccharomyces cerevisiae.对麦芽糖假丝酵母LEU基因进行核苷酸测序分析,该基因可互补大肠杆菌的leuB突变和酿酒酵母的leu2突变。
Curr Genet. 1987;11(6-7):451-7. doi: 10.1007/BF00384606.
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An improved host-vector system for Candida maltosa using a gene isolated from its genome that complements the his5 mutation of Saccharomyces cerevisiae.一种改良的麦芽糖假丝酵母宿主-载体系统,其使用从该酵母基因组中分离出的一个基因,该基因可互补酿酒酵母的his5突变。
Curr Genet. 1989 Oct;16(4):261-6. doi: 10.1007/BF00422112.
Methods Enzymol. 1983;96:663-82. doi: 10.1016/s0076-6879(83)96056-1.
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Cloning of a LEU gene and an ARS site of Candida maltosa.麦芽糖假丝酵母亮氨酸基因和自主复制序列位点的克隆
Gene. 1983 Oct;24(2-3):157-62. doi: 10.1016/0378-1119(83)90075-6.
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Biochem Biophys Res Commun. 1971 Feb 5;42(3):413-9. doi: 10.1016/0006-291x(71)90386-x.
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