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      Glycolate is a Novel Marker of Vitamin B 2 Deficiency Involved in Gut Microbe Metabolism in Mice

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          Abstract

          Microbes in the human gut play a role in the production of bioactive compounds, including some vitamins. Although several studies attempted to identify definitive markers for certain vitamin deficiencies, the role of gut microbiota in these deficiencies is unclear. To investigate the role of gut microbiota in deficiencies of four vitamins, B 2, B 6, folate, and B 12, we conducted a comprehensive analysis of metabolites in mice treated and untreated with antibiotics. We identified glycolate (GA) as a novel marker of vitamin B 2 (VB2) deficiency, and show that gut microbiota sense dietary VB2 deficiency and accumulate GA in response. The plasma GA concentration responded to reduced VB2 supply from both the gut microbiota and the diet. These results suggest that GA is a novel marker that can be used to assess whether or not the net supply of VB2 from dietary sources and gut microbiota is sufficient. We also found that gut microbiota can provide short-term compensation for host VB2 deficiency when dietary VB2 is withheld.

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          The Role of the Microbiome in the Developmental Origins of Health and Disease

          Early-life transient dysbiosis has long-lasting effects on human health, suggesting a role of the microbiome in the DOHaD. Although the prominent role of the microbiome in human health has been established, the early-life microbiome is now being recognized as a major influence on long-term human health and development. Variations in the composition and functional potential of the early-life microbiome are the result of lifestyle factors, such as mode of birth, breastfeeding, diet, and antibiotic usage. In addition, variations in the composition of the early-life microbiome have been associated with specific disease outcomes, such as asthma, obesity, and neurodevelopmental disorders. This points toward this bacterial consortium as a mediator between early lifestyle factors and health and disease. In addition, variations in the microbial intrauterine environment may predispose neonates to specific health outcomes later in life. A role of the microbiome in the Developmental Origins of Health and Disease is supported in this collective research. Highlighting the early-life critical window of susceptibility associated with microbiome development, we discuss infant microbial colonization, beginning with the maternal-to-fetal exchange of microbes in utero and up through the influence of breastfeeding in the first year of life. In addition, we review the available disease-specific evidence pointing toward the microbiome as a mechanistic mediator in the Developmental Origins of Health and Disease.
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            Depiction of metabolome changes in histidine-starved Escherichia coli by CE-TOFMS.

            Metabolic changes in response to histidine starvation were observed in histidine-auxotrophic Escherichia coli using a capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS)-based metabolomics technique. Prior to the analysis, we prepared an E. coli metabolome list of 727 metabolites reported in the literature. An improved method for metabolite extraction was developed, which resulted in higher extraction efficiency in phosphate-rich metabolites, e.g., ATP and GTP. Based on the results, 375 charged, hydrophilic intermediates in primary metabolisms were analysed simultaneously, providing quantitative data of 198 metabolites. We confirmed that the intracellular levels of intermediates in histidine biosynthesis are rapidly accumulated in response to a drop in histidine level under histidine-starved conditions. Simultaneously, disciplined responses were observed in the glycolysis, tricarboxylic acid cycle, and amino acid and nucleotide biosynthesis pathways as regulated by amino acid starvation.
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              Lactic acid bacteria as a cell factory for riboflavin production

              Summary Consumers are increasingly becoming aware of their health and nutritional requirements, and in this context, vitamins produced in situ by microbes may suit their needs and expectations. B groups vitamins are essential components of cellular metabolism and among them riboflavin is one of the vital vitamins required by bacteria, plants, animals and humans. Here, we focus on the importance of microbial production of riboflavin over chemical synthesis. In addition, genetic abilities for riboflavin biosynthesis by lactic acid bacteria are discussed. Genetically modified strains by employing genetic engineering and chemical analogues have been developed to enhance riboflavin production. The present review attempts to collect the currently available information on riboflavin production by microbes in general, while placing greater emphasis on food grade lactic acid bacteria and human gut commensals. For designing riboflavin‐enriched functional foods, proper selection and exploitation of riboflavin‐producing lactic acid bacteria is essential. Moreover, eliminating the in situ vitamin fortification step will decrease the cost of food production.
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                Author and article information

                Journal
                Nutrients
                Nutrients
                nutrients
                Nutrients
                MDPI
                2072-6643
                11 March 2020
                March 2020
                : 12
                : 3
                : 736
                Affiliations
                [1 ]Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University Graduate School, 3-18-15, Kuramoto, Tokushima 770-8503, Japan; sea.by15.koko@ 123456gmail.com (A.Y.); c201831026@ 123456tokushima-u.ac.jp (S.A.); ztyet396@ 123456yahoo.co.jp (M.N.); masuda.rumiko@ 123456tokushima-u.ac.jp (R.M.); shimohata@ 123456tokushima-u.ac.jp (T.S.); mawatari@ 123456tokushima-u.ac.jp (K.M.); akiratak@ 123456tokushima-u.ac.jp (A.T.)
                [2 ]Department of Nutrition, Faculty of Health Science, Hyogo University, 2301, Hiraokacho, Shinzaike, Kakogawa 675-0195, Japan
                Author notes
                [* ]Correspondence: uebanso@ 123456tokushima-u.ac.jp ; Tel.: +81-88-633-9598; Fax: +81-88-633-7092
                [†]

                Authors contributed equally this work and the author order is interchangeable.

                Author information
                https://orcid.org/0000-0003-2880-3801
                Article
                nutrients-12-00736
                10.3390/nu12030736
                7146322
                32168816
                addd35a3-7097-43cc-a69e-ce8c6d88de71
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 February 2020
                : 08 March 2020
                Categories
                Article

                Nutrition & Dietetics
                glycolate,vitamin b2,gut microbe,metabolome
                Nutrition & Dietetics
                glycolate, vitamin b2, gut microbe, metabolome

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