Caldicellulosiruptor Core and Pangenomes Reveal Determinants for Noncellulosomal Thermophilic Deconstruction of Plant Biomass

Author:

Blumer-Schuette Sara E.12,Giannone Richard J.32,Zurawski Jeffrey V.12,Ozdemir Inci12,Ma Qin42,Yin Yanbin42,Xu Ying42,Kataeva Irina42,Poole Farris L.42,Adams Michael W. W.42,Hamilton-Brehm Scott D.32,Elkins James G.32,Larimer Frank W.3,Land Miriam L.32,Hauser Loren J.32,Cottingham Robert W.32,Hettich Robert L.32,Kelly Robert M.12

Affiliation:

1. Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA

2. BioEnergy Science Center, Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA

3. Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA

4. Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, USA

Abstract

ABSTRACT Extremely thermophilic bacteria of the genus Caldicellulosiruptor utilize carbohydrate components of plant cell walls, including cellulose and hemicellulose, facilitated by a diverse set of glycoside hydrolases (GHs). From a biofuel perspective, this capability is crucial for deconstruction of plant biomass into fermentable sugars. While all species from the genus grow on xylan and acid-pretreated switchgrass, growth on crystalline cellulose is variable. The basis for this variability was examined using microbiological, genomic, and proteomic analyses of eight globally diverse Caldicellulosiruptor species. The open Caldicellulosiruptor pangenome (4,009 open reading frames [ORFs]) encodes 106 GHs, representing 43 GH families, but only 26 GHs from 17 families are included in the core (noncellulosic) genome (1,543 ORFs). Differentiating the strongly cellulolytic Caldicellulosiruptor species from the others is a specific genomic locus that encodes multidomain cellulases from GH families 9 and 48, which are associated with cellulose-binding modules. This locus also encodes a novel adhesin associated with type IV pili, which was identified in the exoproteome bound to crystalline cellulose. Taking into account the core genomes, pangenomes, and individual genomes, the ancestral Caldicellulosiruptor was likely cellulolytic and evolved, in some cases, into species that lost the ability to degrade crystalline cellulose while maintaining the capacity to hydrolyze amorphous cellulose and hemicellulose.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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