Comparison of the extracellular proteomes of Escherichia coli B and K-12 strains during high cell density cultivation

被引:76
作者
Xia, Xiao-Xia [1 ,2 ]
Han, Mee-Jung [1 ,2 ]
Lee, Sang Yup [1 ,2 ,3 ,4 ]
Yoo, Jong-Shin [5 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Metab & Biomol Engn Natl Res Lab, BK21 Program,Bioproc Engn Res Ctr,Ctr Syst & Synt, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Inst Biocentury, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[4] Korea Adv Inst Sci & Technol, Bioinformat Res Ctr, Taejon 305701, South Korea
[5] Korea Basic Sci Inst, Taejon, South Korea
关键词
Escherichia coli; extracellular proteome; high cell density cultivation;
D O I
10.1002/pmic.200700826
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Escherichia coli BL21 (DE3) and W3110 strains, belonging to the family B and K-12, respectively, have been most widely employed for recombinant protein production. During the excretory production of recombinant proteins by high cell density cultivation (HCDC) of these strains, other native E. coli proteins were also released. Thus, we analyzed the extracellular proteomes of E. coli BL21 (DE3) and W3110 during HCDC. E. coli BL21 (DE3) released more than twice the amount of protein compared with W3110 during HCDC. A total of 204 protein spots including 83 nonredundant proteins were unambiguously identified by 2-DE and MS. Of these, 32 proteins were conserved in the two strains, while 20 and 33 strain-specific proteins were identified for E. coli BL21 (DE3) and W3110, respectively. More than 70% of identified proteins were found to be of periplasmic origin. The outer membrane proteins, OmpA and OmpF, were most abundant. Two strains showed much different patterns in their released proteins. Also, cell density-dependent variations in the released proteins were observed in both strains. These findings summarized as reference proteome maps will be useful for studying protein release in further detail, and provide new strategies for enhanced excretory production of recombinant proteins.
引用
收藏
页码:2089 / 2103
页数:15
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