Department of Plant and Microbial Biology, University of California, 111 Koshland Hall, Berkeley, CA 94720-3102, USA.
Mol Plant. 2014 Jan;7(1):71-86. doi: 10.1093/mp/sst134. Epub 2013 Oct 24.
Heterologous expression of the isoprene synthase gene in the cyanobacterium Synechocystis PCC 6803 conferred upon these microorganisms the property of photosynthetic isoprene (C₅H₈) hydrocarbons production. Continuous production of isoprene from CO₂ and H₂O was achieved in the light, occurring via the endogenous methylerythritol-phosphate (MEP) pathway, in tandem with the growth of Synechocystis. This work addressed the issue of photosynthetic carbon partitioning between isoprene and biomass in Synechocystis. Evidence is presented to show heterologous genomic integration and cellular expression of the mevalonic acid (MVA) pathway genes in Synechocystis endowing a non-native pathway for carbon flux amplification to isopentenyl-diphosphate (IPP) and dimethylallyl-diphosphate (DMAPP) precursors of isoprene. Heterologous expression of the isoprene synthase in combination with the MVA pathway enzymes resulted in photosynthetic isoprene yield improvement by approximately 2.5-fold, compared with that measured in cyanobacteria transformed with the isoprene synthase gene only. These results suggest that the MVA pathway introduces a bypass in the flux of endogenous cellular substrate in Synechocystis to IPP and DMAPP, overcoming flux limitations of the native MEP pathway. The work employed a novel chromosomal integration and expression of synthetic gene operons in Synechocystis, comprising up to four genes under the control of a single promoter, and expressing three operons simultaneously. This is the first time an entire biosynthetic pathway with seven recombinant enzymes has been heterologously expressed in a photosynthetic microorganism. It constitutes contribution to the genetic engineering toolkit of photosynthetic microorganisms and a paradigm in the pursuit of photosynthetic approaches for the renewable generation of high-impact products.
异源表达异戊二烯合酶基因于集胞藻 PCC 6803 中,赋予这些微生物光合作用异戊二烯(C₅H₈)烃类生产的特性。在光下,通过内源性甲基赤藓醇磷酸(MEP)途径,在集胞藻生长的同时,连续从 CO₂和 H₂O 生产异戊二烯。这项工作解决了集胞藻中光合作用碳分配在异戊二烯和生物量之间的问题。有证据表明,异戊二烯合酶基因在集胞藻中的异源基因组整合和细胞表达赋予了非天然途径,以扩大碳通量到异戊烯基二磷酸(IPP)和二甲基烯丙基二磷酸(DMAPP),异戊二烯的前体。与单独表达异戊二烯合酶的蓝藻相比,异戊二烯合酶与 MVA 途径酶的异源表达使光合作用异戊二烯产量提高了约 2.5 倍。这些结果表明,MVA 途径在集胞藻中引入了一条绕过内源性细胞底物通量的旁路,以 IPP 和 DMAPP,克服了天然 MEP 途径的通量限制。这项工作采用了一种新的染色体整合和表达策略,在集胞藻中合成基因操纵子,由单个启动子控制多达四个基因,并同时表达三个操纵子。这是第一次在光合微生物中异源表达完整的生物合成途径,包含七个重组酶。这为光合微生物的遗传工程工具包做出了贡献,并为可再生生成高影响力产品的光合作用方法提供了范例。