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利用全细胞生物催化剂从槲皮素和蔗糖中经济地一锅合成异槲皮苷和 D-阿洛酮糖。

Economical one-pot synthesis of isoquercetin and D-allulose from quercetin and sucrose using whole-cell biocatalyst.

机构信息

The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, JiangNan University, 1800# Lihu Road, Wuxi, Jiangsu Province 214122, China.

The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, JiangNan University, 1800# Lihu Road, Wuxi, Jiangsu Province 214122, China.

出版信息

Enzyme Microb Technol. 2024 May;176:110412. doi: 10.1016/j.enzmictec.2024.110412. Epub 2024 Feb 15.

DOI:10.1016/j.enzmictec.2024.110412
PMID:38402828
Abstract

Isoquercetin and D-allulose have diverse applications and significant value in antioxidant, antibacterial, antiviral, and lipid metabolism. Isoquercetin can be synthesized from quercetin, while D-allulose is converted from D-fructose. However, their production scale and overall quality are relatively low, leading to high production costs. In this study, we have devised a cost-effective one-pot method for biosynthesizing isoquercetin and D-allulose using a whole-cell biocatalyst derived from quercetin and sucrose. To achieve this, the optimized isoquercetin synthase and D-allulose-3-epimerase were initially identified through isofunctional gene screening. In order to reduce the cost of uridine diphosphate glucose (UDPG) during isoquercetin synthesis and ensure a continuous supply of UDPG, sucrose synthase is introduced to enable the self-circulation of UDPG. At the same time, the inclusion of sucrose permease was utilized to successfully facilitate the catalytic production of D-allulose in whole cells. Finally, the recombinant strain BL21/UGT-SUS+DAE-SUP, which overexpresses MiF3GT, GmSUS, EcSUP, and DAEase, was obtained. This strain co-produced 41±2.4 mg/L of isoquercetin and 5.7±0.8 g/L of D-allulose using 120 mg/L of quercetin and 20 g/L of sucrose as substrates for 5 h after optimization. This is the first green synthesis method that can simultaneously produce flavonoid compounds and rare sugars. These findings provide valuable insights and potential for future industrial production, as well as practical applications in factories.

摘要

异槲皮苷和 D-塔格糖在抗氧化、抗菌、抗病毒和脂质代谢等方面具有广泛的应用和重要价值。异槲皮苷可以从槲皮素合成,而 D-塔格糖则可以从 D-果糖转化而来。然而,它们的生产规模和整体质量相对较低,导致生产成本较高。在本研究中,我们设计了一种使用来源于槲皮素和蔗糖的全细胞生物催化剂来生物合成异槲皮苷和 D-塔格糖的经济高效的一锅法。为了实现这一目标,我们通过同工基因筛选,最初鉴定了优化的异槲皮苷合酶和 D-塔格糖-3-差向异构酶。为了降低异槲皮苷合成过程中尿苷二磷酸葡萄糖(UDPG)的成本并确保 UDPG 的持续供应,引入了蔗糖合酶以实现 UDPG 的自我循环。同时,利用蔗糖通透酶成功地促进了整个细胞中 D-塔格糖的催化生产。最后,获得了过表达 MiF3GT、GmSUS、EcSUP 和 DAEase 的重组菌株 BL21/UGT-SUS+DAE-SUP。该菌株使用 120mg/L 的槲皮素和 20g/L 的蔗糖作为底物,优化后 5 小时内共生产 41±2.4mg/L 的异槲皮苷和 5.7±0.8g/L 的 D-塔格糖。这是首次可以同时生产类黄酮化合物和稀有糖的绿色合成方法。这些发现为未来的工业生产提供了有价值的见解和潜力,以及在工厂中的实际应用。

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