Li Weiwei, He Xiuping, Guo Xuena, Zhang Zhenying, Zhang Borun
Laboratory of Yeast Molecular Genetics and Breeding, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Sheng Wu Gong Cheng Xue Bao. 2009 Oct;25(10):1516-23.
The heterologously expressed L1 protein of human papilomavirus 16 can assembly into virus-like particles (VLPs), which has been used as prophylactic vaccine for cervical carcinoma. To express L1 protein in Hansenula polymorpha, we analyzed the codon usage of the native gene of L1 protein and redesigned the encoding sequence according to the codon bias of H. polymorpha. We used assembly PCR to synthesize the native gene HPV16L1-N and the codon optimized gene HPV16L1. The synthesized genes were cloned into pMOXZa-A vector to generate plasmids pMOXZ-HPV16N and pMOXZ-HPV16. The expression cassettes MOXp-HPV16L1(N)-AOXTT were cloned into YEp352 vector and transferred into H. polymorpha. After methanol inducement, the expression of L1 protein in H. polymorpha was detected from the codon optimized gene HPV16L1 rather than the native gene HPVI6L1-N. The parameters for induced cultivation for strain HP-U-16L with HPV16L1 were investigated in shaking flask cultures. After induced cultivation in YPM (pH 7.0) medium supplemented with methanol to a final concentration of 1.0% every 12 h at 37 degrees C for 72 h, the recombinant produced 78.6 mg/L of L1 protein. This work offers the possibility for the production of prophylactic vaccine for cervical carcinoma by H. polymorpha.
人乳头瘤病毒16型的异源表达L1蛋白可组装成病毒样颗粒(VLPs),该病毒样颗粒已被用作宫颈癌的预防性疫苗。为了在多形汉逊酵母中表达L1蛋白,我们分析了L1蛋白天然基因的密码子使用情况,并根据多形汉逊酵母的密码子偏好性重新设计了编码序列。我们使用组装PCR合成了天然基因HPV16L1-N和密码子优化基因HPV16L1。将合成的基因克隆到pMOXZa-A载体中,构建质粒pMOXZ-HPV16N和pMOXZ-HPV16。将表达盒MOXp-HPV16L1(N)-AOXTT克隆到YEp352载体中,并转入多形汉逊酵母。甲醇诱导后,在多形汉逊酵母中检测到从密码子优化基因HPV16L1而非天然基因HPVI6L1-N表达的L1蛋白。在摇瓶培养中研究了携带HPV16L1的HP-U-16L菌株的诱导培养参数。在37℃下,于YPM(pH 7.0)培养基中每12小时添加终浓度为1.0%的甲醇进行诱导培养72小时后,重组菌产生了78.6 mg/L的L1蛋白。这项工作为利用多形汉逊酵母生产宫颈癌预防性疫苗提供了可能性。