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DdvK,一种新型主要易化超家族转运蛋白,对鞘氨醇单胞菌 SYK-6 菌株摄取 5,5'-脱氢二香草基邻苯二甲酸至关重要。

DdvK, a Novel Major Facilitator Superfamily Transporter Essential for 5,5'-Dehydrodivanillate Uptake by Sphingobium sp. Strain SYK-6.

机构信息

Department of Bioengineering, Nagaoka University of Technology, Nagaoka, Niigata, Japan.

Department of Bioengineering, Nagaoka University of Technology, Nagaoka, Niigata, Japan

出版信息

Appl Environ Microbiol. 2018 Oct 1;84(20). doi: 10.1128/AEM.01314-18. Print 2018 Oct 15.

Abstract

The microbial conversion of lignin-derived aromatics is a promising strategy for the industrial utilization of this large biomass resource. However, efficient application requires an elucidation of the relevant transport and catabolic pathways. In sp. strain SYK-6, most of the enzyme genes involved in 5,5'-dehydrodivanillate (DDVA) catabolism have been characterized, but the transporter has not yet been identified. Here, we identified SLG_07710 () and SLG_07780 (), genes encoding a putative major facilitator superfamily (MFS) transporter and MarR-type transcriptional regulator, respectively. A mutant of SYK-6 completely lost the capacity to grow on and convert DDVA. DdvR repressed the expression of the DDVA -demethylase oxygenase component gene (), while DDVA acted as the gene inducer. A DDVA uptake assay was developed by employing this DdvR-controlled transcriptional regulatory system. A UT26S transformant expressing acquired DDVA uptake capacity, indicating that encodes the DDVA transporter. DdvK, probably requiring the proton motive force, was suggested to be a novel MFS transporter on the basis of the amino acid sequence similarity. Subsequently, we evaluated the effects of overexpression on the production of the DDVA metabolite 2-pyrone-4,6-dicarboxylate (PDC), a building block of functional polymers. A SYK-6 mutant of the PDC hydrolase gene () cultured in DDVA accumulated PDC via 5-carboxyvanillate and grew by utilizing 4-carboxy-2-hydroxypenta-2,4-dienoate. The introduction of a -expression plasmid into a mutant increased the growth rate in DDVA and the amounts of DDVA converted and PDC produced after 48 h by 1.35- and 1.34-fold, respectively. These results indicate that enhanced transporter gene expression can improve metabolite production from lignin derivatives. The bioengineering of bacteria to selectively transport and metabolize natural substrates into specific metabolites is a valuable strategy for industrial-scale chemical production. The uptake of many substrates into cells requires specific transport systems, and so the identification and characterization of transporter genes are essential for industrial applications. A number of bacterial major facilitator superfamily transporters of aromatic acids have been identified and characterized, but many transporters of lignin-derived aromatic acids remain unidentified. The efficient conversion of lignin, an abundant but unutilized aromatic biomass resource, to value-added metabolites using microbial catabolism requires the characterization of transporters for lignin-derived aromatics. In this study, we identified the transporter gene responsible for the uptake of 5,5'-dehydrodivanillate, a lignin-derived biphenyl compound, in sp. strain SYK-6. In addition to characterizing its function, we applied this transporter gene to the production of a value-added metabolite from 5,5'-dehydrodivanillate.

摘要

木质素衍生芳烃的微生物转化是利用这种大型生物质资源的有前途的策略。然而,高效应用需要阐明相关的运输和分解代谢途径。在 sp. 菌株 SYK-6 中,已经对大多数涉及 5,5'-去氢二香草醛 (DDVA) 分解代谢的酶基因进行了特征描述,但尚未鉴定出转运蛋白。在这里,我们鉴定了 SLG_07710 () 和 SLG_07780 (),它们分别编码一个假定的主要易化剂超家族 (MFS) 转运蛋白和 MarR 型转录调节剂。SYK-6 的 突变体完全丧失了在 DDVA 上生长和转化的能力。DdvR 抑制 DDVA-脱甲基酶氧合成分基因 () 的表达,而 DDVA 作为基因诱导剂。通过利用这个由 DdvR 控制的转录调控系统,我们开发了一个 DDVA 摄取测定法。表达 的 UT26S 转化体获得了 DDVA 摄取能力,表明 编码 DDVA 转运蛋白。根据氨基酸序列相似性,DdvK 可能需要质子动力,被认为是一种新型 MFS 转运蛋白。随后,我们评估了 过表达对 DDVA 代谢物 2-吡喃-4,6-二羧酸酯 (PDC) 产量的影响,PDC 是功能聚合物的构建块。在 DDVA 中培养的 PDC 水解酶基因 () 的 SYK-6 突变体通过 5-羧基香草醛积累 PDC,并利用 4-羧基-2-羟基戊-2,4-二烯酸生长。将 -表达质粒引入 突变体中,使 DDVA 中的生长速度和 48 小时后 DDVA 转化和 PDC 产生的量分别提高了 1.35-和 1.34 倍。这些结果表明,增强转运蛋白基因表达可以提高木质素衍生物的代谢产物产量。细菌的生物工程选择性地将天然底物运输和代谢为特定代谢物是工业规模化学生产的一种有价值的策略。许多底物进入细胞需要特定的运输系统,因此鉴定和表征转运蛋白对于工业应用至关重要。已经鉴定和表征了许多芳香酸的细菌主要易化剂超家族转运蛋白,但许多木质素衍生芳香酸的转运蛋白仍未被鉴定。利用微生物分解代谢将木质素这种丰富但未利用的芳香生物质资源转化为增值代谢物,需要对木质素衍生芳烃的转运蛋白进行表征。在这项研究中,我们确定了 sp. 菌株 SYK-6 中 5,5'-去氢二香草醛摄取的转运蛋白基因。除了对其功能进行表征外,我们还将该转运蛋白基因应用于从 5,5'-去氢二香草醛生产增值代谢物。

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