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大肠杆菌中三种输出蛋白的前体。

Precursors of three exported proteins in Escherichia coli.

作者信息

Randall L L, Hardy S J, Josefsson L G

出版信息

Proc Natl Acad Sci U S A. 1978 Mar;75(3):1209-12. doi: 10.1073/pnas.75.3.1209.

DOI:10.1073/pnas.75.3.1209
PMID:349560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC411439/
Abstract

Arabinose-binding protein, maltose-binding protein, and lambda receptor are synthesized in vitro on membrane-bound polysomes from Escherichia coli. All three proteins are exported from the cytoplasm of E. coli and all three are made in vitro in a form a few thousand daltons larger than the authentic protein. The larger form of arabinose-binding protein is also detected in vivo by pulse labeling. It is concluded that the larger forms of the exported proteins are precursors containing an extra sequence. In contrast to the above, when the intracellular protein elongation factor Tu is synthesized in vitro on free polysomes, it is not detectably larger than the authentic form.

摘要

阿拉伯糖结合蛋白、麦芽糖结合蛋白和λ受体在体外由大肠杆菌的膜结合多核糖体合成。这三种蛋白质都从大肠杆菌细胞质中输出,并且这三种蛋白质在体外合成时的形式比真实蛋白质大几千道尔顿。通过脉冲标记在体内也检测到了较大形式的阿拉伯糖结合蛋白。得出的结论是,输出蛋白的较大形式是含有额外序列的前体。与上述情况相反,当细胞内蛋白质延伸因子Tu在游离多核糖体上体外合成时,它与真实形式相比没有明显更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/4f98d2542313/pnas00015-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/ea52065dfc85/pnas00015-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/0818e73ebb0f/pnas00015-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/20beaf42cbce/pnas00015-0172-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/ae73d58e7c99/pnas00015-0172-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/4f98d2542313/pnas00015-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/ea52065dfc85/pnas00015-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/0818e73ebb0f/pnas00015-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/20beaf42cbce/pnas00015-0172-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/ae73d58e7c99/pnas00015-0172-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3161/411439/4f98d2542313/pnas00015-0173-a.jpg

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1
Precursors of three exported proteins in Escherichia coli.大肠杆菌中三种输出蛋白的前体。
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1209-12. doi: 10.1073/pnas.75.3.1209.
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Processing of exported proteins in Escherichia coli.大肠杆菌中输出蛋白的加工过程。
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Studies on the export of the maltose-binding protein and the LamB protein.麦芽糖结合蛋白和LamB蛋白的输出研究。
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Escherichia coli mutants accumulating the precursor of a secreted protein in the cytoplasm.在细胞质中积累分泌蛋白前体的大肠杆菌突变体。
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本文引用的文献

1
An L-arabinose binding protein and arabinose permeation in Escherichia coli.大肠杆菌中的一种L-阿拉伯糖结合蛋白与阿拉伯糖渗透作用
J Mol Biol. 1969 Nov 28;46(1):185-96. doi: 10.1016/0022-2836(69)90065-5.
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Localization of polyribosomes containing alkaline phosphatase nascent polypeptides on membranes of Escherichia coli.含有碱性磷酸酶新生多肽的多核糖体在大肠杆菌膜上的定位。
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Homology in amino-terminal sequence of precursors to pancreatic secretory proteins.胰腺分泌蛋白前体氨基末端序列的同源性。
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Spatial expression of the genome: the signal hypothesis at forty.基因组的空间表达:信号假说四十年。
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Effects of metabolic inhibitors on extracellular fructosyltransferase production in Actinomyces viscosus.代谢抑制剂对粘性放线菌胞外果糖基转移酶产生的影响。
Infect Immun. 1981 Dec;34(3):930-7. doi: 10.1128/iai.34.3.930-937.1981.
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Purification and partial characterization of a putative precursor to staphylococcal enterotoxin B.葡萄球菌肠毒素B假定前体的纯化及部分特性分析
Infect Immun. 1981 Dec;34(3):900-7. doi: 10.1128/iai.34.3.900-907.1981.
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Mechanisms for the incorporation of proteins in membranes and organelles.蛋白质整合到膜和细胞器中的机制。
J Cell Biol. 1982 Jan;92(1):1-22. doi: 10.1083/jcb.92.1.1.
8
ExpA: a conditional mutation affecting the expression of a group of exported proteins in Escherichia coli K-12.实验A:一种影响大肠杆菌K-12中一组输出蛋白表达的条件突变。
Mol Gen Genet. 1981;181(2):192-200. doi: 10.1007/BF00268426.
9
Synthesis and degradation of nitrate reductase in Escherichia coli.大肠杆菌中硝酸还原酶的合成与降解
J Bacteriol. 1981 Apr;146(1):352-9. doi: 10.1128/jb.146.1.352-359.1981.
10
Linkage map of Escherichia coli K-12, edition 6.大肠杆菌K-12连锁图谱,第6版。
Microbiol Rev. 1980 Mar;44(1):1-56. doi: 10.1128/mr.44.1.1-56.1980.
Proc Natl Acad Sci U S A. 1975 Dec;72(12):5016-20. doi: 10.1073/pnas.72.12.5016.
4
Alkaline phosphatase synthesis in a cell-free system using DNA and RNA templates.使用DNA和RNA模板的无细胞体系中碱性磷酸酶的合成。
J Mol Biol. 1977 Feb 15;110(1):75-87. doi: 10.1016/s0022-2836(77)80099-5.
5
The interaction of ribosomes and membranes in animal cells.动物细胞中核糖体与细胞膜的相互作用。
Biochim Biophys Acta. 1976 Oct 26;457(2):171-212. doi: 10.1016/0304-4157(76)90010-1.
6
Marked hydrophobicity of the NH2-terminal extra piece of immunoglobulin light-chain precursors: possible physiological functions of the extra piece.免疫球蛋白轻链前体氨基末端额外片段的显著疏水性:额外片段可能的生理功能。
Proc Natl Acad Sci U S A. 1976 Sep;73(9):3273-7. doi: 10.1073/pnas.73.9.3273.
7
Transfer of proteins across membranes. II. Reconstitution of functional rough microsomes from heterologous components.蛋白质跨膜转运。II. 从异源成分重建功能性糙面微粒体。
J Cell Biol. 1975 Dec;67(3):852-62. doi: 10.1083/jcb.67.3.852.
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Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma.蛋白质跨膜转运。I. 小鼠骨髓瘤膜结合核糖体上经蛋白酶加工和未经加工的新生免疫球蛋白轻链的存在情况
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Eur J Biochem. 1976 Oct 1;69(1):163-7. doi: 10.1111/j.1432-1033.1976.tb10869.x.
10
Synthesis of exported proteins by membrane-bound polysomes from Escherichia coli.大肠杆菌膜结合多核糖体对输出蛋白的合成。
Eur J Biochem. 1977 May 2;75(1):43-53. doi: 10.1111/j.1432-1033.1977.tb11502.x.