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通过组合代谢工程在. 中高效合成藻蓝胆素。

Efficient Synthesis of Phycocyanobilin by Combinatorial Metabolic Engineering in .

机构信息

Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China.

Science Center for Future Foods, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu 214122, China.

出版信息

ACS Synth Biol. 2022 Jun 17;11(6):2089-2097. doi: 10.1021/acssynbio.2c00016. Epub 2022 May 17.

Abstract

Phycocyanobilin (PCB) is a kind of light-harvesting pigment which naturally exists in algae and plays important roles in absorbing and transferring energy. Based on its antioxidant and optical properties, PCB has been applied in food, medicine, and cosmetics. Currently, PCB is mainly extracted from through complicated steps; thus, the biosynthesis of PCB in has attracted more attention. However, due to the lower catalytic efficiency of synthetic enzymes and the deficiency of precursors and cofactors, the titer of PCB remains at a low level. Here, we report the efficient synthesis of PCB by the expression of heme oxygenase-1 from and PCB: ferredoxin oxidoreductase (PcyA) from sp. using a high-copy number plasmid with an inducible T7 promoter and the assembly of these two enzymes at a suitable ratio of 2:1 with DNA scaffolds. Additionally, the synthesis of PCB was further enhanced by direct supplementation of 5-aminolevulinic acid (ALA), moderate overexpression of key enzymes in the heme biosynthetic pathway ( and ), and accelerated cycle of cofactors (NADPH) through the expression of NAD kinase and the addition of a reducing agent. Finally, based on the optimal conditions (Modified R medium with 200 mg/L ALA, 20 mg/L FeSO·7HO, and 5 g/L vitamin C induced by 0.8 mM isopropylthio-β-galactoside at 30 °C), the highest reported titer of PCB (28.32 mg/L) was obtained at the fermenter level by feeding glucose and FeSO·7HO. The strategies applied in this study will be useful for the synthesis of other natural pigments and PCB or heme derivatives in .

摘要

藻蓝蛋白(PCB)是一种天然存在于藻类中的捕光色素,在吸收和传递能量方面发挥着重要作用。基于其抗氧化和光学特性,PCB 已被应用于食品、医药和化妆品领域。目前,PCB 主要通过复杂的步骤从蓝藻中提取;因此,蓝藻中 PCB 的生物合成引起了更多的关注。然而,由于合成酶的催化效率较低,以及前体和辅因子的缺乏,PCB 的产量仍处于较低水平。在这里,我们通过表达来自鱼腥藻 sp.的血红素加氧酶-1(HO-1)和 PCB:铁氧还蛋白氧化还原酶(PcyA),利用带有诱导型 T7 启动子的高拷贝数质粒,并以合适的 2:1 比例与 DNA 支架组装这两种酶,实现了 PCB 的高效合成。此外,通过直接补充 5-氨基乙酰丙酸(ALA)、适度过表达血红素生物合成途径中的关键酶(HO-1 和 ALA 合酶),以及通过表达 NAD 激酶和添加还原剂来加速辅因子(NADPH)循环,进一步增强了 PCB 的合成。最后,在最佳条件下(改良 R 培养基中添加 200 mg/L ALA、20 mg/L FeSO·7HO 和 5 g/L 维生素 C,在 30°C 下用 0.8 mM异丙基硫代-β-D-半乳糖苷诱导),通过补加葡萄糖和 FeSO·7HO,在发酵罐水平上获得了 PCB 的最高报道产量(28.32 mg/L)。本研究中应用的策略将有助于其他天然色素和 PCB 或血红素衍生物在蓝藻中的合成。

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