Degradation of Wheat Straw by Fibrobacter succinogenes S85: a Liquid- and Solid-State Nuclear Magnetic Resonance Study

Wheat straw degradation by Fibrobacter succinogenes was monitored by nuclear magnetic resonance (NMR) spectroscopy and chemolytic methods to investigate the activity of an entire fibrolytic system on an intact complex substrate. In situ solid-state NMR with ¹³C cross-polarization magic angle spinnin...

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Published inApplied and Environmental Microbiology Vol. 71; no. 3; pp. 1247 - 1253
Main Authors Matulova, M, Nouaille, R, Capek, P, Péan, M, Forano, E, Delort, A.-M
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.03.2005
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Summary:Wheat straw degradation by Fibrobacter succinogenes was monitored by nuclear magnetic resonance (NMR) spectroscopy and chemolytic methods to investigate the activity of an entire fibrolytic system on an intact complex substrate. In situ solid-state NMR with ¹³C cross-polarization magic angle spinning was used to monitor the modification of the composition and structure of lignocellulosic fibers (of ¹³C-enriched wheat straw) during the growth of bacteria on this substrate. There was no preferential degradation either of amorphous regions of cellulose versus crystalline regions or of cellulose versus hemicelluloses in wheat straw. This suggests either a simultaneous degradation of the amorphous and crystalline parts of cellulose and of cellulose and hemicelluloses by the enzymes or degradation at the surface at a molecular scale that cannot be detected by NMR. Liquid-state two-dimensional NMR experiments and chemolytic methods were used to analyze in detail the various sugars released into the culture medium. An integration of NMR signals enabled the quantification of oligosaccharides produced from wheat straw at various times of culture and showed the sequential activities of some of the fibrolytic enzymes of F. succinogenes S85 on wheat straw. In particular, acetylxylan esterase appeared to be more active than arabinofuranosidase, which was more active than [alpha]-glucuronidase. Finally, cellodextrins did not accumulate to a great extent in the culture medium.
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Corresponding author. Mailing address for A.-M. Delort: Laboratoire de Synthèse et Etude de Systèmes à Intérêt Biologique, UMR 6504 Université Blaise Pascal-CNRS, 63177 Aubière, France. Phone: 33 473 40 77 14. Fax: 33 473 40 77 17. E-mail: amdelort@chimtp.univ-bpclermont.fr. Mailing address for E. Forano: Unité de Microbiologie, INRA, Centre de Recherches de Clermont-Ferrand-Theix, 63122 Saint-Genès-Champanelle, France. Phone: 33 473 62 42 48. Fax: 33 473 62 45 81. E-mail: forano@clermont.inra.fr.
ISSN:0099-2240
1098-5336
DOI:10.1128/AEM.71.3.1247-1253.2005