Engineering a vanillate-producing strain of Pseudomonas sp. NGC7 corresponding to aromatic compounds derived from the continuous catalytic alkaline oxidation of sulfite lignin.

IF 4.3 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Cell Factories Pub Date : 2024-11-19 DOI:10.1186/s12934-024-02590-z
Mami Kamada, Chieko Yasuta, Yudai Higuchi, Akihiro Yoshida, Irwan Kurnia, Chiho Sakamoto, Aya Takeuchi, Yuta Osaka, Kanami Muraki, Naofumi Kamimura, Eiji Masai, Tomonori Sonoki
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Abstract

Introduction: Lignin is a promising resource for obtaining aromatic materials, however, its heterogeneous structure poses a challenge for effective utilization. One approach to produce homogeneous aromatic materials from lignin involves the application of microbial catabolism, which is gaining attention. This current study focused on constructing a catabolic pathway in Pseudomonas sp. NGC7 to produce vanillate (VA) from aromatic compounds derived from the chemical depolymerization of sulfite lignin.

Results: Alkaline oxidation of sulfite lignin was performed using a hydroxide nanorod copper foam [Cu(OH)2/CF]-equipped flow reactor. The flow reactor operated continuously for 50 h without clogging and it yielded a sulfite lignin stream containing acetovanillone (AV), vanillin (VN), and VA as the major aromatic monomers. The catabolic pathway of Pseudomonas sp. NGC7 was optimized to maximize VA production from aromatic monomers in the sulfite lignin stream derived from this oxidation process. Pseudomonas sp. NGC7 possesses four gene sets for vanillate O-demethylase, comprising the oxygenase component (vanA) and its oxidoreductase component (vanB). Among these, the vanA4B4 gene set was identified as the key contributor to VA catabolism. To facilitate the conversion of AV to VA, AV-converting enzyme genes from Sphingobium lignivorans SYK-6 were introduced. The ΔvanA4B4 strain, harboring these AV-converting genes, produced VA from the sulfite lignin stream with 91 mol%. Further disruption of vanA1B1, vanA2B2, vanA3B3, and a vanillin reductase gene, in addition to vanA4B4, and introduction of a 5-carboxyvanillate decarboxylase gene from S. lignivorans SYK-6 to utilize 5-carboxyvanillin and 5-carboxyvanillate from the sulfite lignin stream for VA production achieved a VA yield of 103 mol%.

Conclusion: Developing methods to overcome lignin heterogeneity is essential for its use as a raw material. Consolidating continuous alkaline oxidation of lignin in a Cu(OH)2/CF-packed flow reactor and biological funneling using an engineered catabolic pathway of Pseudomonas sp. NGC7 is a promising approach to produce VA for aromatic materials synthesis. NGC7 possesses a higher adaptability to various aromatic compounds generated from the alkaline oxidation of lignin and its natural ability to grow on p-hydroxyphenyl, guaiacyl, and syringyl compounds underscores its potential as a bacterial chassis for VA production from a wide range of lignin-derived aromatic compounds.

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培养一株可产生香草醛的假单胞菌 NGC7,该菌株与亚硫酸盐木质素连续催化碱性氧化产生的芳香族化合物相对应。
简介:木质素是一种很有希望获得芳香材料的资源,但其异质结构给有效利用带来了挑战。从木质素中生产均质芳香材料的一种方法是应用微生物分解,这种方法正受到越来越多的关注。本研究的重点是构建假单胞菌 NGC7 的分解途径,从亚硫酸盐木质素化学解聚产生的芳香族化合物中生产香草酸(VA):使用配备氢氧化物纳米泡沫铜[Cu(OH)2/CF]的流动反应器对亚硫酸盐木质素进行碱性氧化。流动反应器连续运行 50 小时无堵塞,产生的亚硫酸盐木质素流中含有乙酰香草酮(AV)、香兰素(VN)和 VA 等主要芳香族单体。对 NGC7 假单胞菌的分解途径进行了优化,以最大限度地从该氧化过程产生的亚硫酸盐木质素流中的芳香族单体中产生 VA。NGC7 假单胞菌拥有四个香草酸 O-脱甲基酶基因组,包括氧合酶成分(vanA)及其氧化还原酶成分(vanB)。其中,vanA4B4 基因组被确定为 VA 分解代谢的主要贡献者。为了促进 AV 向 VA 的转化,引入了来自 Sphingobium lignivorans SYK-6 的 AV 转化酶基因。携带这些 AV 转化基因的 ΔvanA4B4 菌株从亚硫酸盐木质素流中产生的 VA 含量为 91 摩尔%。除vanA4B4外,还进一步破坏了vanA1B1、vanA2B2、vanA3B3和一个香兰素还原酶基因,并引入了S. lignivorans SYK-6的5-羧基香兰素脱羧酶基因,以利用亚硫酸盐木质素流中的5-羧基香兰素和5-羧基香兰素生产VA,VA产量达到103 mol%:开发克服木质素异质性的方法对于将其用作原料至关重要。将木质素在 Cu(OH)2/CF 填料流反应器中的连续碱性氧化和利用假单胞菌 NGC7 的工程化分解途径进行生物漏斗处理结合起来,是生产用于合成芳香材料的醋酸乙烯酯的一种很有前景的方法。NGC7 对木质素碱性氧化产生的各种芳香族化合物具有更高的适应性,它在对羟基苯基、愈创木酰基和丁香酰基化合物上的天然生长能力突出了其作为细菌底盘的潜力,可从广泛的木质素衍生芳香族化合物中生产 VA。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
期刊最新文献
Engineering an Escherichia coli strain for enhanced production of flavonoids derived from pinocembrin. Arthrospira maxima and biosynthesized zinc oxide nanoparticles as antibacterials against carbapenem-resistant Klebsiella pneumoniae and Acinetobacter baumannii: a review article. Engineering a vanillate-producing strain of Pseudomonas sp. NGC7 corresponding to aromatic compounds derived from the continuous catalytic alkaline oxidation of sulfite lignin. Engineering of Saccharomyces cerevisiae as a platform strain for microbial production of sphingosine-1-phosphate. 2-O-α-D-glucosyl glycerol production by whole-cell biocatalyst of lactobacilli encapsulating sucrose phosphorylase with improved glycerol affinity and conversion rate.
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