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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
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We are analyzing https://link.springer.com/article/10.1186/s40168-021-01101-1.

Title:
Review: microbial transformations of human bile acids | Microbiome
Description:
Bile acids play key roles in gut metabolism, cell signaling, and microbiome composition. While the liver is responsible for the production of primary bile acids, microbes in the gut modify these compounds into myriad forms that greatly increase their diversity and biological function. Since the early 1960s, microbes have been known to transform human bile acids in four distinct ways: deconjugation of the amino acids glycine or taurine, and dehydroxylation, dehydrogenation, and epimerization of the cholesterol core. Alterations in the chemistry of these secondary bile acids have been linked to several diseases, such as cirrhosis, inflammatory bowel disease, and cancer. In addition to the previously known transformations, a recent study has shown that members of our gut microbiota are also able to conjugate amino acids to bile acids, representing a new set of “microbially conjugated bile acids.” This new finding greatly influences the diversity of bile acids in the mammalian gut, but the effects on host physiology and microbial dynamics are mostly unknown. This review focuses on recent discoveries investigating microbial mechanisms of human bile acids and explores the chemical diversity that may exist in bile acid structures in light of the new discovery of microbial conjugations. Video Abstract
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Health & Fitness
  • Environment

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't tell how the site generates income.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

bile, acid, bas, pubmed, article, acids, google, scholar, gut, cas, human, conjugated, microbial, cdca, amino, host, activity, salt, microbiota, hydrolase, microbiome, primary, clostridium, diversity, central, metabolism, microbes, glycine, capable, epimerization, disease, pool, conjugation, bsh, udca, accessed, taurine, dca, fig, bacteria, secondary, intestinal, oxidation, characterization, liver, deconjugation, fxr, potential, microbiol, research,

Topics {✒️}

12α-dihydroxy-5β-cholan-24-oic acid 12α-trihydroxy-5β-cholan-24-oic acid 7α-dihydroxy-5β-cholan-24-oic acid 7α-trihydroxy-5β-cholan-24-oic acid 7β-trihydroxy-5β-cholan-24-oic acid 3α-hydroxy-5β-cholan-24-oic acid 12β-trihydroxy-5β-cholan-24-oic acid /jfp/article-pdf/67/12/2772/1676188/0362-028x-67_12_2772 /science/article/abs/pii/s1388198107002156 /science/article/abs/pii/s0039128x05002308 /science/article/abs/pii/s0168165614008050 /science/article/abs/pii/s1383574204000560 /science/article/abs/pii/s0163725819301391 uplc-mrm-ms-validated method bacterium enterocloster bolteae nadph-dependent 7β-hydroxysteroid dehydrogenase yield 3-oxo-δ4-cholyl-coa bile acid profiles /science/article/pii/s0039128x97000433 /science/article/abs/pii/0263785596000185 /science/article/abs/pii/0005274476900681 /science/article/pii/s0039128x08002031 /science/article/abs/pii/0005276088902664 nadp-dependent 12β-hydroxysteroid dehydrogenase yielding 3-oxo-δ4-ca amino acid n-acyltransferase full size image 7-alpha-dehydroxylating bile acids 3-oxo-δ4-cholyl-coa /nar/article/47/d1/d614/5146204 12α-hydroxysteroid dehydrogenase activities amino acid-specific mechanisms position-specific hydroxysteroid dehydrogenase human conjugated ba pool increases /femsle/article-lookup/doi/10 encode 12α-hsdhs [35 bile-acid 7-alpha dehydratase tauro-beta-muricholic acid article download pdf org/cgi-bin/paper org/jem/article-pdf/123/2/413/1082316/413 integrated chemo-enzymatic route putative 12β-hsdh genes genome-based taxonomic classification human bile acid-coa /science/article/pii/0005276077901679 g-protein coupled receptors ba-amino acid conjugates health-related ba research lc-esi-ms/ms

Questions {❓}

  • Bile Acids: A pH Dependent Antibacterial System in the Gut?
  • One may wonder then, why do gut microbiota conjugate our bile acids?
  • Com/action/showPdf?
  • Com/science/article/abs/pii/0005274476900681?
  • Com/science/article/abs/pii/0005276088902664?
  • Com/science/article/abs/pii/0263785596000185?
  • Com/science/article/abs/pii/S0039128X05002308?
  • Com/science/article/abs/pii/S0163725819301391?
  • Com/science/article/abs/pii/S0168165614008050?
  • Com/science/article/abs/pii/S1383574204000560?
  • Com/science/article/abs/pii/S1388198107002156?
  • Com/science/article/pii/S0039128X97000433?
  • Org/cgi-bin/paper?

Schema {🗺️}

WebPage:
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         headline:Review: microbial transformations of human bile acids
         description:Bile acids play key roles in gut metabolism, cell signaling, and microbiome composition. While the liver is responsible for the production of primary bile acids, microbes in the gut modify these compounds into myriad forms that greatly increase their diversity and biological function. Since the early 1960s, microbes have been known to transform human bile acids in four distinct ways: deconjugation of the amino acids glycine or taurine, and dehydroxylation, dehydrogenation, and epimerization of the cholesterol core. Alterations in the chemistry of these secondary bile acids have been linked to several diseases, such as cirrhosis, inflammatory bowel disease, and cancer. In addition to the previously known transformations, a recent study has shown that members of our gut microbiota are also able to conjugate amino acids to bile acids, representing a new set of “microbially conjugated bile acids.” This new finding greatly influences the diversity of bile acids in the mammalian gut, but the effects on host physiology and microbial dynamics are mostly unknown. This review focuses on recent discoveries investigating microbial mechanisms of human bile acids and explores the chemical diversity that may exist in bile acid structures in light of the new discovery of microbial conjugations.
         datePublished:2021-06-14T00:00:00Z
         dateModified:2021-06-14T00:00:00Z
         pageStart:1
         pageEnd:13
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            Cholic acid
            Conjugation
            Microbiome
            Metabolism
            Microbiology
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             Clostridium scindens
             Enterocloster bolteae
            Medical Microbiology
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            Microbial Ecology
            Microbial Genetics and Genomics
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      headline:Review: microbial transformations of human bile acids
      description:Bile acids play key roles in gut metabolism, cell signaling, and microbiome composition. While the liver is responsible for the production of primary bile acids, microbes in the gut modify these compounds into myriad forms that greatly increase their diversity and biological function. Since the early 1960s, microbes have been known to transform human bile acids in four distinct ways: deconjugation of the amino acids glycine or taurine, and dehydroxylation, dehydrogenation, and epimerization of the cholesterol core. Alterations in the chemistry of these secondary bile acids have been linked to several diseases, such as cirrhosis, inflammatory bowel disease, and cancer. In addition to the previously known transformations, a recent study has shown that members of our gut microbiota are also able to conjugate amino acids to bile acids, representing a new set of “microbially conjugated bile acids.” This new finding greatly influences the diversity of bile acids in the mammalian gut, but the effects on host physiology and microbial dynamics are mostly unknown. This review focuses on recent discoveries investigating microbial mechanisms of human bile acids and explores the chemical diversity that may exist in bile acid structures in light of the new discovery of microbial conjugations.
      datePublished:2021-06-14T00:00:00Z
      dateModified:2021-06-14T00:00:00Z
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         Bile acid
         Cholic acid
         Conjugation
         Microbiome
         Metabolism
         Microbiology
         Gut health
          Clostridium scindens
          Enterocloster bolteae
         Medical Microbiology
         Bioinformatics
         Microbial Ecology
         Microbial Genetics and Genomics
         Virology
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            address:
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               type:PostalAddress
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            name:Michigan State University
            address:
               name:Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, USA
               type:PostalAddress
            type:Organization
      name:Robert A. Quinn
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      affiliation:
            name:Michigan State University
            address:
               name:Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, USA
               type:PostalAddress
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      email:[email protected]
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      name:Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, USA
      name:Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, USA
      name:Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, USA

External Links {🔗}(303)

Analytics and Tracking {📊}

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CDN Services {📦}

  • Crossref
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