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在大肠杆菌中,作为sak基因产物输出的必要条件,合成后立即进入输出途径。

Immediate entrance to the export pathway after synthesis as a requirement for export of the sak gene product in Escherichia coli.

作者信息

Sako T

出版信息

J Bacteriol. 1986 Sep;167(3):850-4. doi: 10.1128/jb.167.3.850-854.1986.

DOI:10.1128/jb.167.3.850-854.1986
PMID:3528127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC215951/
Abstract

Export through the cytoplasmic membrane and processing of the sak product in Escherichia coli cells were investigated with E. coli strains carrying pTS301, which produce large amounts of staphylokinase at 42 degrees C. High-level synthesis of the sak product caused transient accumulation not only of the staphylokinase precursor (pSAK) but also of the maltose-binding protein and outer membrane protein A precursors. Thus it was concluded that the sak product shares the export pathway with E. coli secreted proteins at least at a certain step. During high-level synthesis of the sak product, a significant amount of the newly synthesized pSAK remained unprocessed after a chase period, possibly causing the observed accumulation of pSAK. Accumulating pSAK did not mature for a long period, whereas the newly synthesized sak product was exclusively detected in the mature form. These results suggest that it is necessary for the sak product to enter the export pathway during or immediately after synthesis to be exported and processed normally.

摘要

利用携带pTS301的大肠杆菌菌株,研究了葡萄球菌激酶(sak)产物在大肠杆菌细胞中的胞质膜输出及加工过程,该菌株在42℃时可大量产生葡萄球菌激酶。sak产物的高水平合成不仅导致葡萄球菌激酶前体(pSAK)的瞬时积累,还导致麦芽糖结合蛋白和外膜蛋白A前体的瞬时积累。因此得出结论,sak产物至少在某一步骤与大肠杆菌分泌蛋白共享输出途径。在sak产物的高水平合成过程中,经过追踪期后,大量新合成的pSAK仍未加工,这可能是观察到的pSAK积累的原因。积累的pSAK长时间未成熟,而新合成的sak产物仅以成熟形式被检测到。这些结果表明,sak产物在合成期间或合成后立即进入输出途径对于其正常输出和加工是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/58c059072d77/jbacter00208-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/5d4549864489/jbacter00208-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/55afb9463171/jbacter00208-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/d50e1e586934/jbacter00208-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/58c059072d77/jbacter00208-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/5d4549864489/jbacter00208-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/55afb9463171/jbacter00208-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/d50e1e586934/jbacter00208-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b08/215951/58c059072d77/jbacter00208-0103-a.jpg

相似文献

1
Immediate entrance to the export pathway after synthesis as a requirement for export of the sak gene product in Escherichia coli.在大肠杆菌中,作为sak基因产物输出的必要条件,合成后立即进入输出途径。
J Bacteriol. 1986 Sep;167(3):850-4. doi: 10.1128/jb.167.3.850-854.1986.
2
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Export of unprocessed precursor maltose-binding protein to the periplasm of Escherichia coli cells.未加工的前体麦芽糖结合蛋白输出到大肠杆菌细胞的周质中。
J Bacteriol. 1987 Jun;169(6):2352-9. doi: 10.1128/jb.169.6.2352-2359.1987.
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Alterations in the hydrophilic segment of the maltose-binding protein (MBP) signal peptide that affect either export or translation of MBP.麦芽糖结合蛋白(MBP)信号肽亲水片段的改变,这会影响MBP的输出或翻译。
J Bacteriol. 1992 Oct;174(20):6488-97. doi: 10.1128/jb.174.20.6488-6497.1992.
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Expression of the pspA gene stimulates efficient protein export in Escherichia coli.pspA基因的表达可刺激大肠杆菌中的高效蛋白质输出。
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Escherichia coli SecB protein associates with exported protein precursors in vivo.大肠杆菌SecB蛋白在体内与输出的蛋白质前体相结合。
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SecB-independent export of Escherichia coli ribose-binding protein (RBP): some comparisons with export of maltose-binding protein (MBP) and studies with RBP-MBP hybrid proteins.大肠杆菌核糖结合蛋白(RBP)不依赖SecB的输出:与麦芽糖结合蛋白(MBP)输出的一些比较以及对RBP-MBP杂合蛋白的研究。
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The role of the mature part of secretory proteins in translocation across the plasma membrane and in regulation of their synthesis in Escherichia coli.分泌蛋白的成熟部分在大肠杆菌中跨质膜转运及其合成调控中的作用。
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Annu Rev Microbiol. 1982;36:435-65. doi: 10.1146/annurev.mi.36.100182.002251.

引用本文的文献

1
Distinct mutation sites in prlA suppressor mutant strains of Escherichia coli respond either to suppression of signal peptide mutations or to blockage of staphylokinase processing.大肠杆菌prlA抑制突变菌株中的不同突变位点,要么对信号肽突变的抑制有反应,要么对葡萄球菌激酶加工的阻断有反应。
J Bacteriol. 1988 Nov;170(11):5389-91. doi: 10.1128/jb.170.11.5389-5391.1988.
2
Novel prlA alleles defective in supporting staphylokinase processing in Escherichia coli.在大肠杆菌中支持葡萄球菌激酶加工存在缺陷的新型prlA等位基因。
J Bacteriol. 1991 Apr;173(7):2289-96. doi: 10.1128/jb.173.7.2289-2296.1991.

本文引用的文献

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The spontaneous insertion of proteins into and across membranes: the helical hairpin hypothesis.蛋白质自发插入和穿过膜:螺旋发夹假说。
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携带出口特异性抑制突变的大肠杆菌菌株中外膜蛋白和周质蛋白的定位与加工
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Protein localization in E. coli: is there a common step in the secretion of periplasmic and outer-membrane proteins?蛋白质在大肠杆菌中的定位:周质蛋白和外膜蛋白的分泌是否存在共同步骤?
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Evidence for posttranslational translocation of beta-lactamase across the bacterial inner membrane.β-内酰胺酶经细菌内膜进行翻译后转运的证据。
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