0 program (Bendtsen et al., 2004) (http://www.cbs.dtu.dk/services/SignalP). Potential transmembrane domains were determined using either the tmhmm 2.0 (Krogh et al., 2001) (http://www.cbs.dtu.dk/services/TMHMM/) or the tmpred (Hofmann & Stoffel, 1993) (http://www.ch.embnet.org/software/TMPRED_form.html) program. The parameters for molecular mass, theoretical pI, amino acid composition and extinction coefficient were computed using the ProtParam Tool (Gasteiger et al., 2005) on the ExPASy server (http://www.expasy.org/tools/protparam.html).

Pairwise and multiple sequence alignments were performed with the clustalw program (Higgins et al., 1996) using the Network Protein Sequence check details Analysis server (http://npsa-pbil.ibcp.fr/cgi-bin/npsa_automat.pl?page=/NPSA/npsa_clustalw.html). Clostridium thermocellum ATCC 27405 (DSM 1237) is referred to as the type and genome-sequenced strain. Escherichia coli strain XL1-Blue (Stratagene, La Jolla, CA) was used for plasmid constructions, and strain BL21(DE3) (Novagen, Madison, WI) was used for protein overexpression via the T7 RNA polymerase

system. All chemicals were purchased from Sigma Chemical Co. (St Louis, MO) unless otherwise noted. DNA manipulations including genomic DNA preparation, PCR, cloning, ligation and transformation were carried out using standard procedures (Sambrook & Russell, 2001). DNA fragments encoding either CBM3s or PA14 tandem domains were amplified by PCR from C. thermocellum ATCC 27405 genomic DNA, using appropriate

primers HER2 inhibitor as listed in Supporting Information, Table S1. The desired DNA was initially cloned in E. coli XL1-Blue. pET28(+) vector containing the T7 promoter (Novagen) has been used for recombinant protein overexpression procedures. The recombinant CBM3 or PA14 domains fused either to a C- or to an N-terminal hexahistidyl tag (His-tag) were overexpressed in E. coli BL21(DE3). The expression and purification procedure was performed according to a recently published protocol (Jindou et al., 2007). Protein purity was evaluated by sodium dodecyl Fluorouracil cell line sulfate-polyacrylamide gel electrophoresis (12.5%). Qualitative assessment of binding to the insoluble polysaccharides was determined as reported earlier (Xu et al., 2004; Jindou et al., 2006), using Avicel, xylan (from oat), pectin and polygalacturonic acid, all purchased from Sigma Chemical Co., and neutral detergent fibers of alfalfa cell walls, wheat straw and banana fruit stem were prepared as described previously (Van Soest et al., 1991). A small modification of the procedure was made for pectin and polygalacturonic acid that were immersed in buffer containing 7 mM CaCl2 in order to precipitate the polysaccharides (both are soluble in the absence of calcium). Our previous studies on the C.