Institute of Biochemistry, University of Cologne, Zülpicher Str. 47, 50674, Cologne, Germany.
Gutachterbüro U. Borchardt, Hennef (Sieg), Germany.
Microb Cell Fact. 2018 Jun 16;17(1):94. doi: 10.1186/s12934-018-0939-2.
α-D-Glucosylglycerol (αGG) has beneficial functions as a moisturizing agent in cosmetics and potential as a health food material, and therapeutic agent. αGG serves as compatible solute in various halotolerant cyanobacteria such as Synechocystis sp. PCC 6803, which synthesizes αGG in a two-step reaction: The enzymatic condensation of ADP-glucose and glycerol 3-phosphate by GG-phosphate synthase (GGPS) is followed by the dephosphorylation of the intermediate by the GG-phosphate phosphatase (GGPP). The Gram-positive Corynebacterium glutamicum, an industrial workhorse for amino acid production, does not utilize αGG as a substrate and was therefore chosen for the development of a heterologous microbial production platform for αGG.
Plasmid-bound expression of ggpS and ggpP from Synechocystis sp. PCC 6803 enabled αGG synthesis exclusively in osmotically stressed cells of C. glutamicum (pEKEx2-ggpSP), which is probably due to the unique intrinsic control mechanism of GGPS activity in response to intracellular ion concentrations. C. glutamicum was then engineered to optimize precursor supply for αGG production: The precursor for αGG synthesis ADP-glucose gets metabolized by both the glgA encoded glycogen synthase and the otsA encoded trehalose-6-phosphate synthase. Upon deletion of both genes the αGG concentration in culture supernatants was increased from 0.5 mM in C. glutamicum (pEKEx3-ggpSP) to 2.9 mM in C. glutamicum ΔotsA IMglgA (pEKEx3-ggpSP). Upon nitrogen limitation, which inhibits synthesis of amino acids as compatible solutes, C. glutamicum ΔotsA IMglgA (pEKEx3-ggpSP) produced more than 10 mM αGG (about 2 g L).
Corynebacterium glutamicum can be engineered as efficient platform for the production of the compatible solute αGG. Redirection of carbon flux towards αGG synthesis by elimination of the competing pathways for glycogen and trehalose synthesis as well as optimization of nitrogen supply is an efficient strategy to further optimize production of αGG.
α-D-葡萄糖基甘油(αGG)作为化妆品保湿剂具有有益功能,并且具有作为保健品和治疗剂的潜力。αGG 作为各种耐盐蓝藻(如 Synechocystis sp. PCC 6803)的相容溶质,通过两步反应合成:由 GG-磷酸合酶(GGPS)催化 ADP-葡萄糖和甘油 3-磷酸的酶促缩合,然后由 GG-磷酸磷酸酶(GGPP)对中间体进行去磷酸化。革兰氏阳性谷氨酸棒杆菌是生产氨基酸的工业主力,它不以 αGG 为底物,因此被选择用于开发 αGG 的异源微生物生产平台。
来自 Synechocystis sp. PCC 6803 的 ggpS 和 ggpP 质粒结合表达使 αGG 仅在谷氨酸棒杆菌的渗透胁迫细胞中合成(pEKEx2-ggpSP),这可能是由于 GGPS 活性对细胞内离子浓度的独特内在控制机制所致。然后对谷氨酸棒杆菌进行工程改造以优化 αGG 生产的前体供应:αGG 合成的前体 ADP-葡萄糖由编码糖原合酶的 glgA 和编码海藻糖-6-磷酸合酶的 otsA 共同代谢。当同时缺失这两个基因时,培养上清液中的 αGG 浓度从谷氨酸棒杆菌(pEKEx3-ggpSP)中的 0.5mM 增加到谷氨酸棒杆菌ΔotsA IMglgA(pEKEx3-ggpSP)中的 2.9mM。在氮限制下,作为相容溶质的氨基酸合成受到抑制,谷氨酸棒杆菌ΔotsA IMglgA(pEKEx3-ggpSP)产生了超过 10mM 的αGG(约 2g/L)。
谷氨酸棒杆菌可以被工程化为生产相容溶质αGG 的有效平台。通过消除糖原和海藻糖合成的竞争途径以及优化氮源供应来将碳通量重新定向到 αGG 合成,是进一步优化 αGG 生产的有效策略。