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从降解者到生产者:逆转恶臭假单胞菌 KT2440 的没食子酸代谢。

From degrader to producer: reversing the gallic acid metabolism of Pseudomonas putida KT2440.

机构信息

Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, 05508-900, Brazil.

Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, Barcelona, 08003, Spain.

出版信息

Int Microbiol. 2023 May;26(2):243-255. doi: 10.1007/s10123-022-00282-5. Epub 2022 Nov 11.

Abstract

Gallic acid is a powerful antioxidant with multiple therapeutic applications, usually obtained from the acidic hydrolysis of tannins produced by many plants. As this process generates a considerable amount of toxic waste, the use of tannases or tannase-producing microorganisms has become a greener alternative over the last years. However, their high costs still impose some barriers for industrial scalability, requiring solutions that could be both greener and cost-effective. Since Pseudomonas putida KT2440 is a powerful degrader of gallic acid, its metabolism offers pathways that can be engineered to produce it from cheap and renewable carbon sources, such as the crude glycerol generated in biodiesel units. In this study, a synthetic operon with the heterologous genes aroG4, quiC and pobA* was developed and expressed in P. putida, based on an in silico analysis of possible metabolic routes, resulting in no production. Then, the sequences pcaHG and galTAPR were deleted from the genome of this strain to avoid the degradation of gallic acid and its main intermediate, the protocatechuic acid. This mutant was transformed with the vector containing the synthetic operon and was finally able to convert glycerol into gallic acid. Production assays in shaker showed a final concentration of 346.7 ± 0.004 mg L gallic acid after 72 h.

摘要

没食子酸是一种具有多种治疗应用的强大抗氧化剂,通常通过许多植物产生的单宁的酸性水解获得。由于该过程会产生大量有毒废物,因此近年来,使用单宁酶或产单宁酶的微生物已成为一种更环保的替代方法。然而,它们的高成本仍然对工业规模扩大构成了一些障碍,需要既能环保又具有成本效益的解决方案。由于恶臭假单胞菌 KT2440 是没食子酸的强大降解剂,因此其代谢途径可以被工程化,从而可以从廉价且可再生的碳源(例如生物柴油单元中产生的粗甘油)生产没食子酸。在这项研究中,基于可能的代谢途径的计算机分析,开发并在恶臭假单胞菌中表达了带有异源基因 aroG4、quiC 和 pobA*的合成操纵子,但没有产生产物。然后,从该菌株的基因组中删除了 pcaHG 和 galTAPR 序列,以避免没食子酸及其主要中间产物原儿茶酸的降解。该突变体被含有合成操纵子的载体转化,最终能够将甘油转化为没食子酸。在摇瓶中的生产试验中,72 小时后最终浓度达到 346.7±0.004 mg L 的没食子酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace3/10148788/358d9440a93e/10123_2022_282_Fig1_HTML.jpg

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