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Two new gene clusters involved in the degradation of plant cell wall from the fecal microbiota of Tunisian dromedary

Identifieur interne : 000451 ( Main/Exploration ); précédent : 000450; suivant : 000452

Two new gene clusters involved in the degradation of plant cell wall from the fecal microbiota of Tunisian dromedary

Auteurs : Rihab Ameri [Tunisie] ; Elisabeth Laville [France] ; Gabrielle Potocki-Véronèse [France] ; Sahar Trabelsi [Tunisie] ; Monia Mezghani [Tunisie] ; Fatma Elgharbi [Tunisie] ; Samir Bejar [Tunisie]

Source :

RBID : PMC:5877837

Descripteurs français

English descriptors

Abstract

Dromedaries are capable of digesting plant cell wall with high content of lignocellulose of poor digestibility. Consequently, their intestinal microbiota can be a source of novel carbohydrate-active enzymes (CAZymes). To the best of our knowledge, no data are available describing the biochemical analysis of enzymes in dromedary intestinal microbiota. To investigate new hydrolytic enzymes from the dromedary gut, a fosmid library was constructed using metagenomic DNA from feces of non-domestic adult dromedary camels living in the Tunisian desert. High-throughput functional screening of 13756 clones resulted in 47 hit clones active on a panel of various chromogenic and non-chromogenic glycan substrates. Two of them, harboring multiple activities, were retained for further analysis. Clone 26H3 displayed activity on AZO-CM-cellulose, AZCL Carob galactomannan and Tween 20, while clone 36A23 was active on AZCL carob galactomannan and AZCL barley β-glucan. The functional annotation of their sequences highlighted original metagenomic loci originating from bacteria of the Bacteroidetes/Chlorobi group, involved in the metabolization of mannosides and β-glucans thanks to a complete battery of endo- and exo-acting glycoside hydrolases, esterases, phosphorylases and transporters.


Url:
DOI: 10.1371/journal.pone.0194621
PubMed: 29601586
PubMed Central: 5877837


Affiliations:


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<term>Animals (MeSH)</term>
<term>Camelus (microbiology)</term>
<term>Cell Wall (metabolism)</term>
<term>Cell Wall (microbiology)</term>
<term>Cellulose (metabolism)</term>
<term>Feces (microbiology)</term>
<term>Microbiota (genetics)</term>
<term>Molecular Sequence Annotation (MeSH)</term>
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<term>Analyse de séquence (MeSH)</term>
<term>Animaux (MeSH)</term>
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<term>Cellulose (métabolisme)</term>
<term>Chameaux (microbiologie)</term>
<term>Famille multigénique (génétique)</term>
<term>Fèces (microbiologie)</term>
<term>Microbiote (génétique)</term>
<term>Paroi cellulaire (microbiologie)</term>
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<p>Dromedaries are capable of digesting plant cell wall with high content of lignocellulose of poor digestibility. Consequently, their intestinal microbiota can be a source of novel carbohydrate-active enzymes (CAZymes). To the best of our knowledge, no data are available describing the biochemical analysis of enzymes in dromedary intestinal microbiota. To investigate new hydrolytic enzymes from the dromedary gut, a fosmid library was constructed using metagenomic DNA from feces of non-domestic adult dromedary camels living in the Tunisian desert. High-throughput functional screening of 13756 clones resulted in 47 hit clones active on a panel of various chromogenic and non-chromogenic glycan substrates. Two of them, harboring multiple activities, were retained for further analysis. Clone 26H3 displayed activity on AZO-CM-cellulose, AZCL Carob galactomannan and Tween 20, while clone 36A23 was active on AZCL carob galactomannan and AZCL barley β-glucan. The functional annotation of their sequences highlighted original metagenomic loci originating from bacteria of the Bacteroidetes/Chlorobi group, involved in the metabolization of mannosides and β-glucans thanks to a complete battery of endo- and exo-acting glycoside hydrolases, esterases, phosphorylases and transporters.</p>
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