Xia Xiao-Xia, Han Mee-Jung, Lee Sang Yup, Yoo Jong-Shin
Department of Chemical & Biomolecular Engineering, BioProcess Engineering Research Center, Institute for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), Yuseong-gu, Daejeon, Republic of Korea.
Proteomics. 2008 May;8(10):2089-103. doi: 10.1002/pmic.200700826.
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.
大肠杆菌BL21(DE3)和W3110菌株分别属于B族和K - 12族,是重组蛋白生产中应用最为广泛的菌株。在通过这些菌株的高密度培养(HCDC)进行重组蛋白的分泌生产过程中,其他天然大肠杆菌蛋白也会被释放出来。因此,我们分析了大肠杆菌BL21(DE3)和W3110在高密度培养过程中的细胞外蛋白质组。在高密度培养过程中,大肠杆菌BL21(DE3)释放的蛋白量是W3110的两倍多。通过二维电泳(2-DE)和质谱(MS)明确鉴定出总共204个蛋白点,包括83种非冗余蛋白。其中,32种蛋白在这两种菌株中是保守的,而分别为大肠杆菌BL21(DE3)和W3110鉴定出了20种和33种菌株特异性蛋白。发现超过70%的已鉴定蛋白来自周质。外膜蛋白OmpA和OmpF最为丰富。两种菌株释放的蛋白呈现出非常不同的模式。此外,在两种菌株中均观察到释放蛋白的细胞密度依赖性变化。这些作为参考蛋白质组图谱总结的发现将有助于更详细地研究蛋白质释放,并为提高重组蛋白的分泌生产提供新策略。