Eudes Aymerick, Berthomieu Roland, Hao Zhangying, Zhao Nanxia, Benites Veronica Teixeira, Baidoo Edward E K, Loqué Dominique
Joint BioEnergy Institute, EmeryStation East, 5885 Hollis St, 4th Floor, Emeryville, CA 94608, USA; Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA.
Joint BioEnergy Institute, EmeryStation East, 5885 Hollis St, 4th Floor, Emeryville, CA 94608, USA; Ecole Polytechnique, Université Paris-Saclay, Palaiseau 91120, France.
Metab Eng. 2018 Mar;46:13-19. doi: 10.1016/j.ymben.2018.02.002. Epub 2018 Feb 21.
Muconic acid (MA) is a dicarboxylic acid used for the production of industrially relevant chemicals such as adipic acid, terephthalic acid, and caprolactam. Because the synthesis of these polymer precursors generates toxic intermediates by utilizing petroleum-derived chemicals and corrosive catalysts, the development of alternative strategies for the bio-based production of MA has garnered significant interest. Plants produce organic carbon skeletons by harvesting carbon dioxide and energy from the sun, and therefore represent advantageous hosts for engineered metabolic pathways towards the manufacturing of chemicals. In this work, we engineered Arabidopsis to demonstrate that plants can serve as green factories for the bio-manufacturing of MA. In particular, dual expression of plastid-targeted bacterial salicylate hydroxylase (NahG) and catechol 1,2-dioxygenase (CatA) resulted in the conversion of the endogenous salicylic acid (SA) pool into MA via catechol. Sequential increase of SA derived from the shikimate pathway was achieved by expressing plastid-targeted versions of bacterial salicylate synthase (Irp9) and feedback-resistant 3-deoxy-D-arabino-heptulosonate synthase (AroG). Introducing this SA over-producing strategy into engineered plants that co-express NahG and CatA resulted in a 50-fold increase in MA titers. Considering that MA was easily recovered from senesced plant biomass after harvest, we envision the phytoproduction of MA as a beneficial option to add value to bioenergy crops.
粘康酸(MA)是一种二羧酸,用于生产工业相关化学品,如己二酸、对苯二甲酸和己内酰胺。由于这些聚合物前体的合成通过使用石油衍生化学品和腐蚀性催化剂产生有毒中间体,因此开发基于生物的MA生产替代策略引起了广泛关注。植物通过从太阳获取二氧化碳和能量来产生有机碳骨架,因此是构建用于制造化学品的代谢途径的有利宿主。在这项工作中,我们对拟南芥进行了基因工程改造,以证明植物可以作为MA生物制造的绿色工厂。具体而言,质体靶向的细菌水杨酸羟化酶(NahG)和儿茶酚1,2-双加氧酶(CatA)的双重表达导致内源性水杨酸(SA)池通过儿茶酚转化为MA。通过表达质体靶向的细菌水杨酸合酶(Irp9)和反馈抗性3-脱氧-D-阿拉伯庚酮糖酸合酶(AroG),实现了来自莽草酸途径的SA的顺序增加。将这种SA过量生产策略引入共表达NahG和CatA的工程植物中,导致MA产量提高了50倍。考虑到收获后MA很容易从衰老的植物生物质中回收,我们设想MA的植物生产是一种增加生物能源作物价值的有益选择。