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解析木质素增值过程中红球菌中香草醛的代谢分布。

Deciphering the metabolic distribution of vanillin in Rhodococcus opacus during lignin valorization.

机构信息

School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, PR China; Biorefinery Research Institution, Nanjing University of Science and Technology, Nanjing 210094, PR China.

School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, PR China; Biorefinery Research Institution, Nanjing University of Science and Technology, Nanjing 210094, PR China.

出版信息

Bioresour Technol. 2022 Mar;347:126348. doi: 10.1016/j.biortech.2021.126348. Epub 2021 Nov 16.

Abstract

Vanillin bioconversion is important for the biological lignin valorization. In this study, the obscure vanillin metabolic distribution in Rhodoccous opacus PD630 was deciphered by combining the strategies of intermediate detection, putative gene prediction, and target gene verification. The results suggest that approximately 10% (mol/mol) of consumed vanillin is converted to vanillic acid for further metabolism, and a large amount is converted to dead-end vanillyl alcohol in R. opacus PD630. Subsequently, five vanillin reductases were identified in R. opacus PD630, among which Pd630_LPD03722 product exhibited the greatest activity. With the detected metabolic distributions of vanillin, the conversion of vanillin to muconic acid was facilitated by deleting domestic vanillin reductase genes and introducing vanillin dehydrogenase from Sphingobium sp. SYK-6. Ultimately, the muconic acid yield from vanillin increased to 97.83% (mol/mol) from the initial 10% (mol/mol). Moreover, this study demonstrated the existence of vanillin reductases in Escherichia coli, Bacillus subtilis, and Corynebacterium glutamicum.

摘要

香草醛的生物转化对于生物木质素的增值利用非常重要。在这项研究中,我们通过结合中间产物检测、假定基因预测和目标基因验证等策略,揭示了变色栓菌 PD630 中复杂的香草醛代谢分布情况。结果表明,约 10%(摩尔比)的消耗香草醛被转化为香草酸以进一步代谢,而大量的香草醛则在 R. opacus PD630 中转化为无出路的香草基醇。随后,我们在 R. opacus PD630 中鉴定了 5 种香草醛还原酶,其中 Pd630_LPD03722 的产物表现出最大的活性。结合检测到的香草醛代谢分布情况,通过删除国内香草醛还原酶基因并引入鞘氨醇单胞菌 SYK-6 的香草醛脱氢酶,促进了香草醛向黏康酸的转化。最终,香草醛的黏康酸产率从初始的 10%(摩尔比)提高到 97.83%(摩尔比)。此外,本研究还证明了香草醛还原酶在大肠杆菌、枯草芽孢杆菌和谷氨酸棒杆菌中的存在。

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