Juan Bai, Beibei Pan, Wei Luo, Zihan Yang, Lin Zhu, Zhangchen Cheng, Yansheng Zhao, Jiayan Zhang, Ying Zhu, Xiang Xiao
{"title":"植物乳杆菌dy-1硫酸酯酶LPMS在释放大麦麸皮膳食纤维中结合的酚酸中的作用","authors":"Juan Bai, Beibei Pan, Wei Luo, Zihan Yang, Lin Zhu, Zhangchen Cheng, Yansheng Zhao, Jiayan Zhang, Ying Zhu, Xiang Xiao","doi":"10.1111/1750-3841.70062","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n \n <p>Latic acid fermentation is an effective way to release the bound phenolic acids from grains dietary fiber to improve the biological effects in vivo. Previous analysis of whole genome sequencing and comparative proteomics has revealed that a sulfatase named LPMS in <i>Lactiplantibacillus plantarum</i> dy-1 (<i>L. plantarum</i> dy-1) was the potential key enzyme in promoting the release of bound phenol from barley bran dietary fiber. In this present study, we utilized gene editing technology to modify dy-1 to verify the key role of LPMS in releasing the bond phenolic acids during dy-1 fermentation. Results showed that <i>lpms</i> knockout and overexpression strains (dy-1-∆LPMS and dy-1-OELPMS) were successfully constructed, evidenced by the <i>lpms</i> gene level and sequencing. <i>lpms</i> editing delayed the exponential period of dy-1 growth but had little effect on the stable period. Fermented barley bran dietary fiber (FBDF) by dy-1, dy-1-∆LPMS, and dy-1-OELPMS demonstrated lower molecular weight, rougher surface morphology, looser microstructure, and decreased crystallinity, among which dy-1-∆LPMS showed the least influence. Confocal laser scanning microscope results illustrated that the colocalization between bound phenolic acids and dietary fibers was more apparent under dy-1-ΔLPMS fermentation. Furthermore, knockout of <i>lpms</i> significantly declined the release of bond phenolic acids, especially for the hydroxybenzoic acid derivatives, resulting in the lower antioxidant capacities (<i>p</i> < 0.05). In all, we confirmed that the sulfatase LPMS in <i>L. plantarum</i> dy-1 played great part in releasing the bond phenolic acids from barley bran dietary fiber, therefore improving the bioactivity of released phenolic acids.</p>\n </section>\n \n <section>\n \n <h3> Practical Application</h3>\n \n <p>This study confirmed the sulfatase LPMS in <i>L. plantarum</i> dy-1 played key role in releasing the bond phenolic acids during fermentation of barley bran dietary fiber. In the future, heterologously expressed LPMSs have great potential applications in the brewing and feed industries, among others, which could increase the nutritional and commercial value of byproducts.</p>\n </section>\n </div>","PeriodicalId":193,"journal":{"name":"Journal of Food Science","volume":"90 2","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Role of sulfatase LPMS from Lactiplantibacillus plantarum dy-1 in releasing bound phenolic acids of barley bran dietary fiber\",\"authors\":\"Juan Bai, Beibei Pan, Wei Luo, Zihan Yang, Lin Zhu, Zhangchen Cheng, Yansheng Zhao, Jiayan Zhang, Ying Zhu, Xiang Xiao\",\"doi\":\"10.1111/1750-3841.70062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <section>\\n \\n \\n <p>Latic acid fermentation is an effective way to release the bound phenolic acids from grains dietary fiber to improve the biological effects in vivo. Previous analysis of whole genome sequencing and comparative proteomics has revealed that a sulfatase named LPMS in <i>Lactiplantibacillus plantarum</i> dy-1 (<i>L. plantarum</i> dy-1) was the potential key enzyme in promoting the release of bound phenol from barley bran dietary fiber. In this present study, we utilized gene editing technology to modify dy-1 to verify the key role of LPMS in releasing the bond phenolic acids during dy-1 fermentation. Results showed that <i>lpms</i> knockout and overexpression strains (dy-1-∆LPMS and dy-1-OELPMS) were successfully constructed, evidenced by the <i>lpms</i> gene level and sequencing. <i>lpms</i> editing delayed the exponential period of dy-1 growth but had little effect on the stable period. Fermented barley bran dietary fiber (FBDF) by dy-1, dy-1-∆LPMS, and dy-1-OELPMS demonstrated lower molecular weight, rougher surface morphology, looser microstructure, and decreased crystallinity, among which dy-1-∆LPMS showed the least influence. Confocal laser scanning microscope results illustrated that the colocalization between bound phenolic acids and dietary fibers was more apparent under dy-1-ΔLPMS fermentation. Furthermore, knockout of <i>lpms</i> significantly declined the release of bond phenolic acids, especially for the hydroxybenzoic acid derivatives, resulting in the lower antioxidant capacities (<i>p</i> < 0.05). In all, we confirmed that the sulfatase LPMS in <i>L. plantarum</i> dy-1 played great part in releasing the bond phenolic acids from barley bran dietary fiber, therefore improving the bioactivity of released phenolic acids.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Practical Application</h3>\\n \\n <p>This study confirmed the sulfatase LPMS in <i>L. plantarum</i> dy-1 played key role in releasing the bond phenolic acids during fermentation of barley bran dietary fiber. 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引用次数: 0
摘要
乳酸发酵是释放谷物膳食纤维中结合的酚酸以提高体内生物效应的有效途径。先前的全基因组测序和比较蛋白质组学分析表明,植物乳杆菌dy-1 (L. plantarum dy-1)中一种名为LPMS的磺化酶可能是促进大麦麸皮膳食纤维中结合苯酚释放的关键酶。在本研究中,我们利用基因编辑技术对dy-1进行修饰,验证了LPMS在dy-1发酵过程中释放键酚酸的关键作用。结果显示,成功构建了lpms敲除株和过表达株(dy-1-∆lpms和dy-1- oelpms),证实了lpms基因水平和测序结果。LPMS编辑延迟了dy-1生长的指数期,但对稳定期影响不大。经dy-1、dy-1-∆LPMS和dy-1- oelpms发酵的大麦麸皮膳食纤维分子量降低,表面形貌粗糙,微观结构疏松,结晶度降低,其中对dy-1-∆LPMS影响最小。共聚焦激光扫描显微镜结果表明,在dy-1-ΔLPMS发酵过程中,结合的酚酸与膳食纤维的共定位更为明显。此外,敲除lpms显著降低了键型酚酸的释放,特别是对羟基苯甲酸衍生物的释放,导致抗氧化能力降低(p <;0.05)。综上所述,我们证实了L. plantarum day -1中的硫酸酯酶LPMS在释放大麦麸皮膳食纤维中的键性酚酸中发挥了重要作用,从而提高了所释放的酚酸的生物活性。本研究证实了L. plantarum day -1中的硫酸酯酶LPMS在大麦麸膳食纤维发酵过程中释放结合酚酸中起关键作用。在未来,异源表达的lpms在酿造和饲料等行业具有很大的应用潜力,可以提高副产品的营养价值和商业价值。
Role of sulfatase LPMS from Lactiplantibacillus plantarum dy-1 in releasing bound phenolic acids of barley bran dietary fiber
Latic acid fermentation is an effective way to release the bound phenolic acids from grains dietary fiber to improve the biological effects in vivo. Previous analysis of whole genome sequencing and comparative proteomics has revealed that a sulfatase named LPMS in Lactiplantibacillus plantarum dy-1 (L. plantarum dy-1) was the potential key enzyme in promoting the release of bound phenol from barley bran dietary fiber. In this present study, we utilized gene editing technology to modify dy-1 to verify the key role of LPMS in releasing the bond phenolic acids during dy-1 fermentation. Results showed that lpms knockout and overexpression strains (dy-1-∆LPMS and dy-1-OELPMS) were successfully constructed, evidenced by the lpms gene level and sequencing. lpms editing delayed the exponential period of dy-1 growth but had little effect on the stable period. Fermented barley bran dietary fiber (FBDF) by dy-1, dy-1-∆LPMS, and dy-1-OELPMS demonstrated lower molecular weight, rougher surface morphology, looser microstructure, and decreased crystallinity, among which dy-1-∆LPMS showed the least influence. Confocal laser scanning microscope results illustrated that the colocalization between bound phenolic acids and dietary fibers was more apparent under dy-1-ΔLPMS fermentation. Furthermore, knockout of lpms significantly declined the release of bond phenolic acids, especially for the hydroxybenzoic acid derivatives, resulting in the lower antioxidant capacities (p < 0.05). In all, we confirmed that the sulfatase LPMS in L. plantarum dy-1 played great part in releasing the bond phenolic acids from barley bran dietary fiber, therefore improving the bioactivity of released phenolic acids.
Practical Application
This study confirmed the sulfatase LPMS in L. plantarum dy-1 played key role in releasing the bond phenolic acids during fermentation of barley bran dietary fiber. In the future, heterologously expressed LPMSs have great potential applications in the brewing and feed industries, among others, which could increase the nutritional and commercial value of byproducts.
期刊介绍:
The goal of the Journal of Food Science is to offer scientists, researchers, and other food professionals the opportunity to share knowledge of scientific advancements in the myriad disciplines affecting their work, through a respected peer-reviewed publication. The Journal of Food Science serves as an international forum for vital research and developments in food science.
The range of topics covered in the journal include:
-Concise Reviews and Hypotheses in Food Science
-New Horizons in Food Research
-Integrated Food Science
-Food Chemistry
-Food Engineering, Materials Science, and Nanotechnology
-Food Microbiology and Safety
-Sensory and Consumer Sciences
-Health, Nutrition, and Food
-Toxicology and Chemical Food Safety
The Journal of Food Science publishes peer-reviewed articles that cover all aspects of food science, including safety and nutrition. Reviews should be 15 to 50 typewritten pages (including tables, figures, and references), should provide in-depth coverage of a narrowly defined topic, and should embody careful evaluation (weaknesses, strengths, explanation of discrepancies in results among similar studies) of all pertinent studies, so that insightful interpretations and conclusions can be presented. Hypothesis papers are especially appropriate in pioneering areas of research or important areas that are afflicted by scientific controversy.