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The xyl-doc gene cluster of Ruminiclostridium cellulolyticum encodes GH43- and GH62-?-l-arabinofuranosidases with complementary modes of action.


ABSTRACT: Background:The ?-l-arabinofuranosidases (?-l-ABFs) are exoenzymes involved in the hydrolysis of ?-l-arabinosyl linkages in plant cell wall polysaccharides. They play a crucial role in the degradation of arabinoxylan and arabinan and they are used in many biotechnological applications. Analysis of the genome of R. cellulolyticum showed that putative cellulosomal ?-l-ABFs are exclusively encoded by the xyl-doc gene cluster, a large 32-kb gene cluster. Indeed, among the 14 Xyl-Doc enzymes encoded by this gene cluster, 6 are predicted to be ?-l-ABFs belonging to the CAZyme families GH43 and GH62. Results:The biochemical characterization of these six Xyl-Doc enzymes revealed that four of them are ?-l-ABFs. GH4316-1229 (RcAbf43A) which belongs to the subfamily 16 of the GH43, encoded by the gene at locus Ccel_1229, has a low specific activity on natural substrates and can cleave off arabinose decorations located at arabinoxylan chain extremities. GH4310-1233 (RcAbf43Ad2,3), the product of the gene at locus Ccel_1233, belonging to subfamily 10 of the GH43, can convert the double arabinose decorations present on arabinoxylan into single O2- or O3-linked decorations with high velocity (k cat?=?16.6?±?0.6 s-1). This enzyme acts in synergy with GH62-1234 (RcAbf62Am2,3), the product of the gene at locus Ccel_1234, a GH62 ?-l-ABF which hydrolyzes ?-(1???3) or ?-(1???2)-arabinosyl linkages present on polysaccharides and arabinoxylooligosaccharides monodecorated. Finally, a bifunctional enzyme, GH62-CE6-1240 (RcAbf62Bm2,3Axe6), encoded by the gene at locus Ccel_1240, which contains a GH62-?-l-ABF module and a carbohydrate esterase (CE6) module, catalyzes deacylation of plant cell wall polymers and cleavage of arabinosyl mono-substitutions. These enzymes are also active on arabinan, a component of the type I rhamnogalacturonan, showing their involvement in pectin degradation. Conclusion:Arabinofuranosyl decorations on arabinoxylan and pectin strongly inhibit the action of xylan-degrading enzymes and pectinases. ?-l-ABFs encoded by the xyl-doc gene cluster of R. cellulolyticum can remove all the decorations present in the backbone of arabinoxylan and arabinan, act synergistically, and, thus, play a crucial role in the degradation of plant cell wall polysaccharides.

SUBMITTER: Mroueh M 

PROVIDER: S-EPMC6556953 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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The <i>xyl</i>-<i>doc</i> gene cluster of <i>Ruminiclostridium cellulolyticum</i> encodes GH43- and GH62-α-l-arabinofuranosidases with complementary modes of action.

Mroueh Mohamed M   Aruanno Marion M   Borne Romain R   de Philip Pascale P   Fierobe Henri-Pierre HP   Tardif Chantal C   Pagès Sandrine S  

Biotechnology for biofuels 20190610


<h4>Background</h4>The α-l-arabinofuranosidases (α-l-ABFs) are exoenzymes involved in the hydrolysis of α-l-arabinosyl linkages in plant cell wall polysaccharides. They play a crucial role in the degradation of arabinoxylan and arabinan and they are used in many biotechnological applications. Analysis of the genome of <i>R. cellulolyticum</i> showed that putative cellulosomal α-l-ABFs are exclusively encoded by the <i>xyl</i>-<i>doc</i> gene cluster, a large 32-kb gene cluster. Indeed, among the  ...[more]

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