Cheng Danhui, Wang Ri, Prather Kristala Jones, Chow King Lau, Hsing I-Ming
Bioengineering Graduate Program, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong; Division of Biomedical Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.
Departmental of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Enzyme Microb Technol. 2015 May;72:25-34. doi: 10.1016/j.enzmictec.2015.02.003. Epub 2015 Feb 16.
The photosynthetic Rhodobacter species are promising alternative expression hosts in bioproduction and biorefinery due to their unique metabolic capacities. With prominent inner membrane areas and efficient endogenous translocation machineries, they are especially attractive for membrane protein expression. However, codon usage bias could be a limitation in the engineering of Rhodobacter species and has seldom been investigated. In this study, we tackled the codon bias of Rhodobacter by functionally expressing 8 rare tRNAs of Rhodobacter sphaeroides with a multi-copy vector. The impact of tRNA supplementation was evaluated through monitoring expression levels of two heterologous proteins with different phylogenetic origins, a membrane subunit of the riboflavin transporter, RibU, from Lactobacillus acidophilus La-14 and a decaheme cytochrome, MtrA, from Shewanella oneidensis. Our results showed that the performances were closely related to medium composition and rare codon percentages of raw DNA sequences. Provision of rare tRNAs has increased RibU production by 7.7-folds and 2.86-fold in minimal medium and rich medium, respectively, while MtrA levels were increased by 1-fold in minimal medium. The present study confirms the presence of codon bias in R. sphaeroides and offers a facile tool for improving heterologous expression of rare-codon containing genes. We anticipate that this tRNA supplementation system can be further extended to other species of Rhodobacter, and thus will facilitate the engineering of purple bacteria for interesting applications in microbial technology.
光合红杆菌属因其独特的代谢能力,在生物生产和生物精炼中是很有前景的替代表达宿主。由于其显著的内膜面积和高效的内源性转运机制,它们对于膜蛋白表达尤其具有吸引力。然而,密码子使用偏好可能是红杆菌属工程改造中的一个限制因素,并且很少有人对此进行研究。在本研究中,我们通过用多拷贝载体功能性表达球形红杆菌的8种稀有tRNA来解决红杆菌属的密码子偏好问题。通过监测两种具有不同系统发育起源的异源蛋白的表达水平来评估tRNA补充的影响,这两种蛋白分别是嗜酸乳杆菌La-14的核黄素转运蛋白的膜亚基RibU和希瓦氏菌的十血红素细胞色素MtrA。我们的结果表明,表达情况与培养基组成和原始DNA序列的稀有密码子百分比密切相关。提供稀有tRNA分别使RibU在基本培养基和丰富培养基中的产量提高了7.7倍和2.86倍,而MtrA在基本培养基中的水平提高了1倍。本研究证实了球形红杆菌中存在密码子偏好,并提供了一种简便的工具来改善含稀有密码子基因的异源表达。我们预计这种tRNA补充系统可以进一步扩展到其他红杆菌属物种,从而将促进紫色细菌的工程改造,以用于微生物技术中的有趣应用。