The Translational Coupling of Daidzein Reductase and Dihydrodaidzein Racemase Genes Improves the Production of Equol and Its Analogous Derivatives in Engineered Lactic Acid Bacteria.

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Susana Langa, José Antonio Curiel, Ángela Peirotén, José María Landete
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引用次数: 0

Abstract

Equol (EQ) and its analogous derivatives 5-hydroxy-equol (5-OH-EQ) and 5-hydroxy-dehydroequol (5-OH-D-EQ) are isoflavones which benefit human health. They are produced from daidzein and genistein, respectively, in the gut by microorganisms harboring the genes daidzein reductase (dzr), dihydrodaidzein racemase (ifcA), dihydrodaidzein reductase (ddr) and tetrahydrodaidzein reductase (tdr). Since the production of these isoflavones is of interest due to their great-health benefits for humans, the heterologous expression of dzr, ddr, tdr and ifcA from Slackia isoflavoniconvertenes DSM 22006T in lactic acid bacteria (LAB) was used as a strategy to produce EQ, 5-OH-EQ and 5-OH-D-EQ in soy beverages. However, efficient production of these compounds was only demonstrated in two engineered Limosilactobacillus fermentum strains, and it is dependent on dihydrodaidzein racemase (DDRC). In order to increase the production of EQ and its analogous derivatives in different LAB species and genera, different strategies were performed with the ifcA gene. Translational coupling of ifcA and dzr genes (pNZ:TuR.dzr.ifcA) under the influence of a constitutive promoter improved the efficiency of production of EQ, 5-OH-EQ and 5-OH-D-EQ in the engineered LAB strains. The translational coupling of ifcA and dzr genes allowed the production of high concentrations of eq (111.15 ± 9.20-410.56 ± 24.15 μM), 5-OH-eq (71.00 ± 4.25 μM-148.22 ± 9.15 μM) and 5-OH-D-eq (111.15 ± 9.20-201.09 ± 7.65 μM) in soy beverages by different engineered LAB genera, such as L. fermentum INIA 584L, Lactilactobacillus plantarum WCFS1, and Lactocaseibacillus paracasei BL23. Translational coupling has allowed engineered Laboratories strains belonging to different genera, such as L. fermentum, L. plantarum, and L. paracasei, to produce high concentrations of EQ, 5-OH-EQ and 5-OH-D-EQ. Translational coupling could be exploited as a strategy for the efficient production of bioactive compounds.

大豆苷元还原酶和二氢大豆苷元消旋酶基因的翻译偶联提高了工程乳酸菌雌马酚及其类似衍生物的产量。
雌马酚(EQ)及其类似衍生物5-羟基雌马酚(5-OH-EQ)和5-羟基脱氢雌马酚(5-OH-D-EQ)是有益人体健康的异黄酮。它们分别由肠道中含有大豆蛋白还原酶(dzr)、二氢大豆蛋白消消酶(ifcA)、二氢大豆蛋白还原酶(ddr)和四氢大豆蛋白还原酶(tdr)基因的微生物产生。由于这些异黄酮的生产因其对人类的巨大健康益处而引起人们的兴趣,因此将Slackia异黄酮DSM 22006T的dzr, ddr, tdr和ifcA在乳酸菌(LAB)中的异源表达作为在大豆饮料中生产EQ, 5-OH-EQ和5-OH-D-EQ的策略。然而,这些化合物的高效生产仅在两种工程发酵乳酸杆菌菌株中得到证实,并且依赖于二氢大豆苷元消旋酶(DDRC)。为了在不同的LAB种和属中增加EQ及其类似衍生物的产量,对ifcA基因采取了不同的策略。在本构启动子的影响下,ifcA和dzr基因(pNZ: turr .dzr.ifcA)的翻译偶联提高了工程LAB菌株中EQ、5-OH-EQ和5-OH-D-EQ的生产效率。ifcA和dzr基因的翻译偶联使得不同的工程LAB属(如发酵乳杆菌INIA 584L、植物乳杆菌WCFS1和副干酪乳杆菌BL23)在大豆饮料中产生高浓度的eq(111.15±9.20-410.56±24.15 μM)、5-OH-eq(71.00±4.25 μM-148.22±9.15 μM)和5-OH-D-eq(111.15±9.20-201.09±7.65 μM)。翻译耦合使得不同属的工程实验室菌株,如发酵乳杆菌、植物乳杆菌和副乳杆菌,能够产生高浓度的EQ、5-OH-EQ和5-OH-D-EQ。翻译偶联可以作为一种有效生产生物活性化合物的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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