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Carbohydrates and Gut Microbiota

Carbohydrates and Gut Microbiota

Accept All Anti-inflammatory sleep tips All Show Purposes. Nat Rev Micrboiota Hepatol — Carboyhdrates J, Abu-Ali G, Huttenhower Carbohydrates and Gut Microbiota. Food Security Ans Center, Microibota of Abd Nutrition, Isfahan University Carbohydrates and Gut Microbiota Medical Sciences, Isfahan, Iran. A breach in the epithelial layer as a result of inflammation could subsequently lead to the transfer of LPS across the epithelial layer into the blood circulation, resulting in endotoxemia. Sauerkraut, kimchi, pickles, olives and tempeh "have the fiber and polyphenols to support a healthy gut microbiome, and also deliver living microbes [probiotics] that provide added benefits. Glucose, mannose and glucosamine were preferentially consumed by Bacteroidales compared with the other orders, whereas lactulose was mainly produced by Eubacteriales Extended Data Fig.

Carbohydrates and Gut Microbiota -

Xu H, Li X, Adams H, Kubena K, Guo S. Etiology of metabolic syndrome and dietary intervention. Int J Mol Sci. Ju S-Y, Lee J-Y, Kim D-H. Association of metabolic syndrome and its components with all-cause and cardiovascular mortality in the elderly: a meta-analysis of prospective cohort studies.

Article PubMed PubMed Central Google Scholar. Ward ZJ, Bleich SN, Cradock AL, Barrett JL, Giles CM, Flax C, et al. Projected US state-level prevalence of adult obesity and severe obesity.

N Engl J Med. Article PubMed Google Scholar. Finkelstein EA, Khavjou OA, Thompson H, Trogdon JG, Pan L, Sherry B, et al. Obesity and severe obesity forecasts through Am J Prev Med. Ervin RB. Prevalence of metabolic syndrome among adults 20 years of age and over, by sex, age, race and ethnicity, and body mass index; United States, ; Google Scholar.

Aguilar M, Bhuket T, Torres S, Liu B, Wong RJ. Prevalence of the metabolic syndrome in the United States, Article CAS PubMed Google Scholar. Farmanfarma KK, Kaykhaei MA, Adineh HA, Mohammadi M, Dabiri S, Ansari-Moghaddam A. Prevalence of metabolic syndrome in Iran: a meta-analysis of 69 studies.

Diabetes Metab Syndr Clin Res Rev. Article Google Scholar. Dalvand S, Niksima SH, Meshkani R, Gheshlagh RG, Sadegh-Nejadi S, Kooti W, et al.

Prevalence of metabolic syndrome among Iranian population: a systematic review and meta-analysis. Iran J Public Health. PubMed PubMed Central Google Scholar. Lozupone CA, Stombaugh JI, Gordon JI, Jansson JK, Knight R. Diversity, stability and resilience of the human gut microbiota.

Article CAS PubMed PubMed Central Google Scholar. Ursell LK, Haiser HJ, Van Treuren W, Garg N, Reddivari L, Vanamala J, et al. The intestinal metabolome: an intersection between microbiota and host. The gut flora as a forgotten organ. EMBO Rep.

Brunkwall L, Orho-Melander M. The gut microbiome as a target for prevention and treatment of hyperglycaemia in type 2 diabetes: from current human evidence to future possibilities. Alkahtani S, Elkilany A, Alhariri M.

Association between sedentary and physical activity patterns and risk factors of metabolic syndrome in Saudi men: a cross-sectional study. BMC Public Health. Song M, Chan AT. Environmental factors, gut microbiota, and colorectal cancer prevention. Clin Gastroenterol Hepatol. Nielsen DS, Krych Ł, Buschard K, Hansen CH, Hansen AK.

Beyond genetics. Influence of dietary factors and gut microbiota on type 1 diabetes. FEBS Lett. Dabke K, Hendrick G, Devkota S. The gut microbiome and metabolic syndrome. J Clin Investig. Wang P-X, Deng X-R, Zhang C-H, Yuan H-J. Gut microbiota and metabolic syndrome. Chin Med J. Dietary strategies for management of metabolic syndrome: role of gut microbiota metabolites.

Carding S, Verbeke K, Vipond DT, Corfe BM, Owen LJ. Dysbiosis of the gut microbiota in disease. Microb Ecol Health Dis. PubMed Google Scholar. Petersen C, Round JL.

Defining dysbiosis and its influence on host immunity and disease. Cell Microbiol. Parekh PJ, Balart LA, Johnson DA. The influence of the gut microbiome on obesity, metabolic syndrome and gastrointestinal disease.

Clin Transl Gastroenterol. Diet-microbiota interactions and their implications for healthy living. Dong TS, Luu K, Lagishetty V, Sedighian F, Woo S-L, Dreskin BW, et al. A high protein calorie restriction diet alters the gut microbiome in obesity. Bhute SS, Mefferd CC, Phan JR, Ahmed M, Fox-King AE, Alarcia S, Villarama JV, Abel-Santos E, Hedlund BP.

A high-carbohydrate diet prolongs dysbiosis and clostridioides difficile carriage and increases delayed mortality in a hamster model of infection. Microbiol Spectr. Esposito K, Giugliano D. Mediterranean diet and the metabolic syndrome: the end of the beginning. Metab Syndr Relat Disord.

Azadbakht L, Mirmiran P, Esmaillzadeh A, Azizi T, Azizi F. Beneficial effects of a dietary approaches to stop hypertension eating plan on features of the metabolic syndrome.

Diabetes Care. Johnson RJ, Segal MS, Sautin Y, Nakagawa T, Feig DI, Kang D-H, et al. Potential role of sugar fructose in the epidemic of hypertension, obesity and the metabolic syndrome, diabetes, kidney disease, and cardiovascular disease.

Am J Clin Nutr. CAS PubMed Google Scholar. Volek JS, Feinman RD. Carbohydrate restriction improves the features of metabolic syndrome. metabolic syndrome may be defined by the response to carbohydrate restriction.

Nutr Metab Lond. Mandayam S, Mitch WE. Dietary protein restriction benefits patients with chronic kidney disease. Muzio F, Mondazzi L, Harris WS, Sommariva D, Branchi A. Effects of moderate variations in the macronutrient content of the diet on cardiovascular disease risk factors in obese patients with the metabolic syndrome.

Feinman RD, Volek JS, Westman EC. Dietary carbohydrate restriction in the treatment of diabetes and metabolic syndrome. Clin Nutr Insight. Hyde PN, Sapper TN, Crabtree CD, LaFountain RA, Bowling ML, Buga A, et al.

Dietary carbohydrate restriction improves metabolic syndrome independent of weight loss. JCI Insight. Kimiagar SM, Ghaffarpour M, Houshiar Rad A, Hormozdyari H, Zellipour L.

Food consumption pattern in the Islamic Republic of Iran and its relation to coronary heart disease; Book Google Scholar. Esmaillzadeh A, Mirmiran P, Azizi F. Whole-grain intake and the prevalence of hypertriglyceridemic waist phenotype in Tehranian adults.

Rajaie S, Azadbakht L, Khazaei M, Sherbafchi M, Esmaillzadeh A. Moderate replacement of carbohydrates by dietary fats affects features of metabolic syndrome: a randomized crossover clinical trial. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, et al.

Radakovich K, Heilbrun LK, Venkatranamamoorthy R, Lababidi S, Klurfeld DM, Djuric ZJN, et al. Women participating in a dietary intervention trial maintain dietary changes without much effect on household members. Nutr Cancer. Bradley R, Kozura E, Buckle H, Kaltunas J, Tais S, Standish LJ.

Description of clinical risk factor changes during naturopathic care for type 2 diabetes. J Altern Complement Med New York, NY. Lim MY, You HJ, Yoon HS, Kwon B, Lee JY, Lee S, et al. The effect of heritability and host genetics on the gut microbiota and metabolic syndrome.

Festi D, Schiumerini R, Eusebi LH, Marasco G, Taddia M, Colecchia A. World J Gastroenterol. Hollis S, Campbell F. What is meant by intention to treat analysis? Survey of published randomised controlled trials. Shao J, Zhong B. Last observation carry-forward and last observation analysis.

Stat Med. Saklayen MG. The global epidemic of the metabolic syndrome. Curr Hypertens Rep. Mazidi M, Pennathur S, Afshinnia F. Link of dietary patterns with metabolic syndrome: analysis of the National Health and Nutrition Examination Survey.

Nutr Diabetes. Hu T, Yao L, Reynolds K, Niu T, Li S, Whelton P, et al. The effects of a low-carbohydrate diet on appetite: a randomized controlled trial. Nutr Metab Cardiovasc Dis. Gildner TE. Links between metabolic syndrome and the microbiome. Evol Med Public Health.

Flandroy L, Poutahidis T, Berg G, Clarke G, Dao M-C, Decaestecker E, et al. The impact of human activities and lifestyles on the interlinked microbiota and health of humans and of ecosystems.

Sci Total Environ. Leeming ER, Johnson AJ, Spector TD, Le Roy CI. Effect of diet on the gut microbiota: rethinking intervention duration. Download references. Patients and members of the general public were not involved in formulating the research question, study, recruitment, conduct, or report.

After the study, we will distribute the results via social media to the participants. This study will be funded by grants from Tehran University of Medical Sciences TUMS No.

Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. Obesity and Eating Habits Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Ld, lipid droplets; Ml, Muscle layer; Gc, Goblet cell; Gv, Gut villus. In addition, we examined pH and lysozyme activity of hindgut content in three groups Table 5.

Table 5. The evaluation of gut structure and physiological environment in intestinal samples of this study. We assessed gut permeability using the paracellular tracer FITC-dextran just prior to the end of the experiment.

We also examined the relative mRNA levels of genes related to gut permeability Figure 7F. Figure 8. The evaluation of gut inflammation in three treatments.

A Histological results of hindgut by hematoxylin and eosin staining, Original magnification is ×; B Relative mRNA levels of pNF- κ B and PAI ; C Relative mRNA levels of Tumor Necrosis Factor α TNF- α and IL-I β.

C0 group and C10 group demonstrate the normal physiological features of the gut villus, whereas C20 group shows severe pathological changes.

Ic, Inflammatory cell; Ml, Muscle layer; Gc, Goblet cell; Gv, Gut villus. Up to now, many nutritional factors have been reported to affect gut microbial community structure, including resistant starch Warren et al.

The novelty of the present work lies in the comprehensive characterization of gut microbial communities in Chinese perch after being fed with different contents of gelatinized starch diets and their correlation with gut health.

In the present study, gut microbial community diversity of Chinese perch was significantly decreased after feeding with high-starch diet, suggesting that supplementation of gelatinized starch to diet can also reshape gut microbiota, just like high-fructose, and high-glucose and high-fat diets Li et al.

However, the change trend of gut microbiota composition in Chinese perch was significantly different from that in mammals after feeding with high carbohydrate diet. In mice, Firmicutes -to- Bacteroidetes ratios and proportions of Proteobacteria are significantly were increased Do et al.

Our results indicated that the proportion of Tenericutes was increased gradually with the increase in dietary gelatinized starch content, and that Tenericutes became the absolute dominant bacteria in gut micro-organisms after long-term feeding with high dietary gelatinized starch in Chinese perch, thus the growth space of other bacteria was compressed to a certain extent, result in no significant increase in the proportion of Firmicutes -to- Bacteroidetes ratios or proportions of Proteobacteria.

As a representative species of Tenericutes , Mycoplasma is a kind of bacteria using carbohydrate as main energy substance Gupta et al. Mycoplasma is rare in gut microbial community of mammalian when animals are under normal feeding or high carbohydrates feeding.

However, Mycoplasma is common species in gut microbial community of aquatic animals Dong et al. We speculated that this might be due to the fact that carbohydrate is the first energy substance for mammals and can be rapidly absorbed and utilized, while it is not the first energy substance for fish Wilson, Since most fishes are extremely intolerant to carbohydrate and cannot quickly absorb and use it, mycoplasma make full use of sufficient carbohydrate as the main source of energy to propagate rapidly and influence the abundance of other bacteria.

High carbohydrate diet-induced damage in gut might be associated with the changes in gut microbiota and permeability in mammals. However, the key role of gut microbiota and related metabolites in the process of high carbohydrate diet-induced inflammation has not been well-elucidated.

Our study indicated that the relative abundances of Gram-negative bacteria and butyric acid-producing bacteria were also significantly decreased due to the proliferation of Tenericutes , which had a great impact on gut health in the high gelatinized starch diet group. Gram-negative bacteria are the main source of LPS Cani et al.

In mammals, the change in gut microbiota composition can increase LPS production level by Gram-negative bacteria Szabo, However, our study showed the opposite result that the change in gut microbiota composition significantly decreased LPS content in chyme in high gelatinized starch diet group, compared with control group, which was beneficial to the gut health to a certain extent.

Butyrate is an important energy source for gut enterocytes Chen et al. Lack of butyric acid can result in gut permeability increase Wu et al. In this experiment, the gut permeability was significantly increased, and butyrate content was sharply decreased due to the reduction in the relative abundance of butyric acid producing bacteria.

In addition, high gelatinized starch diets caused gut lipid metabolism disorders in Chinese perch, further resulting in the deposition of a large amount of lipid droplets in gut, which might have a direct effect on gut structure and gut function. Based on these results, it could be concluded that butyric acid deficiency and gut lipid droplet excessive accumulation cause an increase in gut permeability, thus causing more LPS to penetrate into the plasma, finally causing inflammation infiltration in the gut tract Figure 9B.

Our finding is consistent with the results of LPS-induced inflammatory infiltration in mammals Kim et al. Further, this study provides more details about the relationship between gut microbiota and gut health. Mycoplasma and butyric acid-producing bacteria play a key role in the whole process in non-mammals.

The mechanism underlying destroying gut health by high-starch diet was elaborated in non-mammals for first time. This study may provide data basis for the effective application of butyric acid-producing bacteria or butyric acid in high-starch diet.

Figure 9. Mechanism by which different contents of gelatinized starch diet influence the gut health. High gelatinized starch diets cause gut microbial changes and lipid metabolism disorders, which further leads to inflammation. However, the moderate amount of gelatinized starch in diets is beneficial to the health of gut Figure 9A.

The health of gut is largely determined by the acidity and alkalinity of gut environment Kohl et al. Previous study has reported that in an alkaline environment, the abundance of beneficial bacteria, such as lactic acid bacteria, was decreased, that of harmful bacteria was increased, resulting in gut immune function decline Jeurissen et al.

In this experiment, moderate gelatinized starch diets caused an increase in gut microbiota diversity relative to control group, and the relative abundance of many beneficial bacteria was significantly improved relative to control group at genera level, including Lactococcus , Lactobacillus , Geobacillus , Clostridium , Bifidobacterium , and so on.

We also found that the pH of gut chyme was decreased significantly and lactic acid content was increased significantly in C10 group, with the increase in relative abundance of Lactobacilli and Bifidobacteria.

Thus, a weakly acidic environment occurred in gut, which in turn promoted the growth of beneficial bacteria and the formation of a virtuous circle Sissons, In such a good environment, gut wall thickness and villus length was increased, and the gut absorption surface area was expanded, which was beneficial to the nutrient absorption in gut Sissons, According to the predictive functional profiles of microbial communities determined by PICRUSt analysis, the top ten most abundant functions were shown in Figure 5 , and the obvious differences in level 3 KEGG pathways were observed among the three groups Table 4.

Membrane transport pathways, such as transporters and ABC transporters, are essential for cell survival and growth and crucial for the survival of microbiota in gut ecosystem Lyons et al. The research demonstrated that such predicted transporter functions were connected with nutrient-associated changes in gut microbiota composition Odamaki et al.

In this experiment, the proportion of transporters was significantly increased in moderate gelatinized starch diet group, while this change was reversed in the high gelatinized starch diet group.

This indicated that the addition of gelatinized starch to diet was important for the changes in the microbiota of gut, and that the addition of an appropriate amount of gelatinized starch was beneficial to gut microbiota, enabling the microbial community to utilize the nutrients better in gut by enhancing membrane transport pathways.

The level of energy metabolism and metabolism of cofactors and vitamins in gut microbiota are related to the growth of gut microbiota and the state of body.

One previous study has shown that high-grain diets lead to gut inflammation and dramatical increase in energy metabolism pathway levels of gut microbiota in goats Zhang et al. Another study has reported that energy metabolic pathways in gut microbiota were significantly increased in spring samples, which could facilitate a Tibetan Macaques Macaca thibetana recovery from acute energy loss experienced during winter Sun et al.

In addition, the metabolism level of cofactors and vitamins in late-instar Spodoptera littoralis in gut microbiota was significantly higher than that in the early instar larva Chen et al.

These studies suggested that gut microbiota might respond to stimuli from the inside or outside of the body by significantly increasing energy metabolism and the metabolism of coenzyme factors and vitamins. Our results further demonstrate that microbiota play a key role in the gut damage caused by the high-carbohydrate diet.

Our findings make the targeted regulation of gut microbiota possible to mitigate the damage caused by the increase in starch content in feed of fish. In summary, we demonstrate that ordinary dietary gelatinized starch significantly alters gut microbiota composition in Chinese perch. Furthermore, this study makes the first comprehensive illustration of the action mechanisms and the specific regulatory effects of high carbohydrate diet-modulated microbiota on gut health of non-mammals.

Our results reveal that Mycoplasma and butyric acid-producing bacteria play a key role in the above process. The datasets presented in this study can be found in online repositories. The animal study was reviewed and approved by the Ethics Committee of the Institute of Laboratory Animal Centre, Huazhong Agriculture University.

YZ, X-FL, and SH designed the experiments and helped to draft the manuscript. YZ, XC, JW, JL, QZ, ZZ, LL, and MA performed the experiments.

All authors read and approved the final manuscript. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Asaduzzaman, M. Effects of carbohydrate source for maintaining a high C: N ratio and fish driven re-suspension on pond ecology and production in periphyton-based freshwater prawn culture systems.

Aquaculture , 37— doi: CrossRef Full Text Google Scholar. Baumgartner, S. The effects of amoxicillin and vancomycin on parameters reflecting cholesterol metabolism. Lipids , — PubMed Abstract CrossRef Full Text Google Scholar. Boulangé, C. Impact of the gut microbiota on inflammation, obesity, and metabolic disease.

Genome Med. Google Scholar. Boursier, J. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology 63, — Cani, P. Metabolic endotoxemia initiates obesity and insulin resistance.

Diabetes 56, — Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet—induced obesity and diabetes in mice.

Diabetes 57, — Caporaso, J. QIIME allows analysis of high-throughput community sequencing data. Methods 7, — Chen, B. Biodiversity and activity of the gut microbiota across the life history of the insect herbivore Spodoptera littoralis.

Chen, X. Effects of intravenous infusion with sodium butyrate on colonic microbiota, intestinal development-and mucosal immune-related gene expression in normal growing pigs.

Cummings, J. Role of intestinal bacteria in nutrient metabolism. De Baere, S. Development of a HPLC—UV method for the quantitative determination of four short-chain fatty acids and lactic acid produced by intestinal bacteria during in vitro fermentation.

De Lartigue, G. Vagal afferent neurons in high fat diet-induced obesity; intestinal microflora, gut inflammation and cholecystokinin. Do, M. High-glucose or-fructose diet cause changes of the gut microbiota and metabolic disorders in mice without body weight change.

Nutrients Dong, J. Comparative analysis of the intestinal bacterial community and expression of gut immunity genes in the Chinese Mitten Crab Eriocheir sinensis.

AMB Express Enes, P. Effect of normal and waxy maize starch on growth, food utilization and hepatic glucose metabolism in European sea bass Dicentrarchus labrax juveniles. A , 89— Galfi, P. Feeding trial in pigs with a diet containing sodium n-butyrate.

Acta Vet. Garling, D. Effects of dietary carbohydrate to lipid ratios on growth and body composition of fingerling channel catfish. Fish Cult. Gupta, R. Phylogenetic framework for the phylum Tenericutes based on genome sequence data: proposal for the creation of a new order Mycoplasmoidales ord. and Metamycoplasmataceae fam.

harbouring Eperythrozoon , Ureaplasma and five novel genera. Antonie Van Leeuwenhoek , — Hamer, H. The role of butyrate on colonic function. Hemre, G. Carbohydrates in fish nutrition: effects on growth, glucose metabolism and hepatic enzymes.

Hibberd, A. Probiotic or synbiotic alters the gut microbiota and metabolism in a randomised controlled trial of weight management in overweight adults. Microbes 10, — Hutchins, C. Lairson, L. Glycosyltransferases: structures, functions, and mechanisms.

Boraston, A. Carbohydrate-binding modules: fine-tuning polysaccharide recognition. Davies, G. Recent structural insights into the expanding world of carbohydrate-active enzymes.

Koshland, D. Stereochemistry and the mechanism of enzymatic reactions. Article CAS Google Scholar. Berlemont, R. Glycoside hydrolases across environmental microbial communities. PLoS Comput. Danby, P. Advances in enzymatic glycoside synthesis. ACS Chem. Nishimoto, M.

Practical preparation of lacto- N -biose I, a candidate for the Bifidus factor in human milk. Liu, Q. Bacterial glycosidases for the production of universal red blood cells. Rahfeld, P. An enzymatic pathway in the human gut microbiome that converts A to universal O type blood.

This paper highlights how functional metagenomics can be applied for discovery of enzymes with therapeutic potential from within the gut microbiome. Muegge, B. Diet drives convergence in gut microbiome functions across mammalian phylogeny and within humans.

Science , — Sonnenburg, E. The ancestral and industrialized gut microbiota and implications for human health. Groussin, M. Unraveling the processes shaping mammalian gut microbiomes over evolutionary time. Freter, R. Mechanisms that control bacterial populations in continuous-flow culture models of mouse large intestinal flora.

Wu, G. Linking long-term dietary patterns with gut microbial enterotypes. Tap, J. Gut microbiota richness promotes its stability upon increased dietary fibre intake in healthy adults.

Makki, K. The impact of dietary fiber on gut microbiota in host health and disease. Cell Host Microbe 23 , — Vangay, P. US immigration westernizes the human gut microbiome. Cell , — e10 Smits, S. Seasonal cycling in the gut microbiome of the Hadza hunter-gatherers of Tanzania.

David, L. Diet rapidly and reproducibly alters the human gut microbiome. De Filippis, F. Unusual sub-genus associations of faecal Prevotella and Bacteroides with specific dietary patterns. Microbiome 4 , 57 Article PubMed PubMed Central Google Scholar.

Zaramela, L. Gut bacteria responding to dietary change encode sialidases that exhibit preference for red meat-associated carbohydrates.

Leeming, E. Effect of diet on the gut microbiota: rethinking intervention duration. Nutrients 11 , Article PubMed Central Google Scholar.

Diet-induced extinctions in the gut microbiota compound over generations. Hehemann, J. Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes. Natl Acad. USA , — This paper provides key insights into how new capabilities for carbohydrate degradation can be obtained by gut bacteria via horizontal gene transfer.

Pluvinage, B. Molecular basis of an agarose metabolic pathway acquired by a human intestinal symbiont. Transfer of carbohydrate-active enzymes from marine bacteria to Japanese gut microbiota. Cerqueira, F. Starch digestion by gut bacteria: crowdsourcing for carbs.

Trends Microbiol. Anderson, K. Biochemical evidence that starch breakdown by Bacteroides thetaiotaomicron involves outer membrane starch-binding sites and periplasmic starch-degrading enzymes. This seminal work describes the first characterization of Sus from B.

Genetic evidence that outer membrane binding of starch is required for starch utilization by Bacteroides thetaiotaomicron. Brown, H. Host glycan utilization within the Bacteroidetes Sus-like paradigm.

Glycobiology 31 , — Cuskin, F. Human gut Bacteroidetes can utilize yeast mannan through a selfish mechanism. Luis, A. Dietary pectic glycans are degraded by coordinated enzyme pathways in human colonic Bacteroides.

Rakoff-Nahoum, S. The evolution of cooperation within the gut microbiota. An ecological network of polysaccharide utilization among human intestinal symbionts. Cartmell, A. A surface endogalactanase in Bacteroides thetaiotaomicron confers keystone status for arabinogalactan degradation.

Sobala, L. An epoxide intermediate in glycosidase catalysis. ACS Cent. This study provides key experimental evidence for a substrate-assisted mechanism proceeding through a 1,2-epoxide intermediate by GH99 family members, one of the most recently elucidated glycoside hydrolase mechanisms.

Valguarnera, E. Surface exposure and packing of lipoproteins into outer membrane vesicles are coupled processes in Bacteroides. mSphere 3 , e Briggs, J. Communal living: glycan utilization by the human gut microbiota. Article PubMed Google Scholar.

Ndeh, D. Complex pectin metabolism by gut bacteria reveals novel catalytic functions. Nature , 65—70 This tour de force offers insights into the coordination of carbohydrate degradation by gut bacteria, identifies several new CAZy families and revises the structure of RG-II one of the most complex dietary glycans known.

Tamura, K. Molecular mechanism by which prominent human gut bacteroidetes utilize mixed-linkage β-glucans, major health-promoting cereal polysaccharides.

Cell Rep. Rogowski, A. Glycan complexity dictates microbial resource allocation in the large intestine. Lozupone, C. Diversity, stability and resilience of the human gut microbiota. Lapébie, P. Bacteroidetes use thousands of enzyme combinations to break down glycans.

Laine, R. Invited commentary: A calculation of all possible oligosaccharide isomers both branched and linear yields 1. Glycobiology 4 , — Terrapon, N. PULDB: the expanded database of polysaccharide utilization loci.

Despres, J. Xylan degradation by the human gut Bacteroides xylanisolvens XB1AT involves two distinct gene clusters that are linked at the transcriptional level.

BMC Genomics 17 , Corfield, A. The interaction of the gut microbiota with the mucus barrier in health and disease in human. Microorganisms 6 , 78 Article CAS PubMed Central Google Scholar.

Interactions of commensal and pathogenic microorganisms with the intestinal mucosal barrier. Ficko-Blean, E. Insights into the recognition of the human glycome by microbial carbohydrate-binding modules.

Sonnenburg, J. Getting a grip on things: how do communities of bacterial symbionts become established in our intestine? Tailford, L. Mucin glycan foraging in the human gut microbiome.

Briliūtė, J. Complex N-glycan breakdown by gut Bacteroides involves an extensive enzymatic apparatus encoded by multiple co-regulated genetic loci. This paper provides insights into how B. thetaiotaomicron utilizes extensive enzymatic machinery to carry out the degradation of structural variants of complex N-glycans.

Article PubMed CAS Google Scholar. Prospecting for microbial α- N -acetylgalactosaminidases yields a new class of GH31 O-glycanase. Mucosal glycan foraging enhances fitness and transmission of a saccharolytic human gut bacterial symbiont.

Cell Host Microbe 4 , — Pudlo, N. Symbiotic human gut bacteria with variable metabolic priorities for host mucosal glycans. MBio 6 , e—15 Derrien, M. Akkermansia muciniphila and its role in regulating host functions. Hooper, L. A molecular sensor that allows a gut commensal to control its nutrient foundation in a competitive ecosystem.

USA 96 , — Bry, L. A model of host—microbial interactions in an open mammalian ecosystem. Benjdia, A. Sulfatases and radical SAM enzymes: emerging themes in glycosaminoglycan metabolism and the human microbiota. Varki, A. Nothing in glycobiology makes sense, except in the light of evolution.

A single sulfatase is required to access colonic mucin by a gut bacterium. Crouch, L. Prominent members of the human gut microbiota express endo-acting O-glycanases to initiate mucin breakdown.

This work first identifies surface-localized endolytic glycoside hydrolases acting on O-glycans in Bacteroides as had been observed in other PULs but not against O-glycans and as such provided insights into degradation of mucosal glycans by gut bacteria.

Noach, I. Recognition of protein-linked glycans as a determinant of peptidase activity. USA , E—E This insightful work first illustrated the molecular basis of glycoprotease activity. Shon, D. An enzymatic toolkit for selective proteolysis, detection, and visualization of mucin-domain glycoproteins.

Haurat, M. The glycoprotease CpaA secreted by medically relevant Acinetobacter species targets multiple O-linked host glycoproteins. mBio 11 , e—20 Malaker, S. The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins. Architecturally complex O-glycopeptidases are customized for mucin recognition and hydrolysis.

USA , e Hughes, G. The MUC5B mucin polymer is dominated by repeating structural motifs and its topology is regulated by calcium and pH. Renzi, F. Glycan-foraging systems reveal the adaptation of Capnocytophaga canimorsus to the dog mouth. mBio 6 , e—e Reily, C.

Glycosylation in health and disease. Fairbanks, A. The ENGases: versatile biocatalysts for the production of homogeneous N-linked glycopeptides and glycoproteins. Knapp, S. NAG-Thiazoline, an N -acetyl-β-hexosaminidase inhibitor that implicates acetamido participation.

Vocadlo, D. Detailed comparative analysis of the catalytic mechanisms of β- N -acetylglucosaminidases from families 3 and 20 of glycoside hydrolases. Biochemistry 44 , — Trastoy, B.

Structural basis of mammalian high-mannose N-glycan processing by human gut Bacteroides. Nihira, T. Discovery of β-1,4- d -mannosyl- N -acetyl- d -glucosamine phosphorylase involved in the metabolism of N-glycans.

Higgins, M. N-Glycan degradation pathways in gut- and soil-dwelling Actinobacteria share common core genes. Cordeiro, R. N-Glycan utilization by Bifidobacterium gut symbionts involves a specialist β-mannosidase.

How members of the human gut microbiota overcome the sulfation problem posed by glycosaminoglycans. This work illustrates how B. thetaiotaomicron tackles the degradation of host glycosaminoglycans with highly variable sulfation patterns, specifically heparin and heparan sulfate.

A hierarchical classification of polysaccharide lyases for glycogenomics. Nakamichi, Y. Crystal structure of a bacterial unsaturated glucuronyl hydrolase with specificity for heparin. Recognition and degradation of plant cell wall polysaccharides by two human gut symbionts.

Raghavan, V. Tuning transcription of nutrient utilization genes to catabolic rate promotes growth in a gut bacterium. Metabolism of multiple glycosaminoglycans by Bacteroides thetaiotaomicron is orchestrated by a versatile core genetic locus.

Pellock, S. Glucuronides in the gut: sugar-driven symbioses between microbe and host. Bolleddula, J. Carbon—carbon bond cleavage and formation reactions in drug metabolism and the role of metabolic enzymes.

Drug Metab. Wallace, B. Alleviating cancer drug toxicity by inhibiting a bacterial enzyme. Kong, R. Old drug new use — amoxapine and its metabolites as potent bacterial β-glucuronidase inhibitors for alleviating cancer drug toxicity.

Cancer Res. Pollet, R. An atlas of β-glucuronidases in the human intestinal microbiome. Structure 25 , — e5 Ervin, S.

Targeting regorafenib-induced toxicity through inhibition of gut microbial β-glucuronidases. Creekmore, B. Mouse gut microbiome-encoded β-glucuronidases identified using metagenome analysis guided by protein structure.

To circumvent this potential Mivrobiota problem, we aimed at providing an overview about whether Carbohydrates and Gut Microbiota how dietary supplementation of Carbohyddrates complex Carbohydrates and Gut Microbiota Microboita the gut microbiome in healthy non-obese Micribiota. We then reviewed whether the Carbohhydrates changes in Carbohydrztes bacterial members found to be established by complex Gut health and healthy lifestyle would benefit or Mucrobiota the cardiometabolic Carbohydrates and Gut Microbiota immunological health of the host taking into account the alterations in the microbiome composition and abundance known to be associated with obesity and its associated disorders. By combining these research areas, we aimed to give a better insight into the potential of foods containing complex carbohydrates in the treatment and prevention of above-mentioned diseases. We conclude that supplemental complex carbohydrates that increase Bifidobacteria and Lactobacilli, without increasing the deleterious Bacteroidesare most likely promoting cardiometabolic and immunological health in obese subjects. Overall, this review article shows that whereas it is relatively clear in which direction supplemental fermentable carbohydrates can alter the gut microbiome, the relevance of these changes regarding health remains controversial. Carbohydrates and Gut Microbiota

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