MOESM7 of Unraveling essential cellulosomal components of the (Pseudo)Bacteroides cellulosolvens reveals an extensive reservoir of novel catalytic enzymes

Additional file 7: Table S4. Mass spectrometry analysis of normalized GH-containing proteins. The intensities of all the proteins in four cellulosomal fractions (CB I, CB II, MCC I and MCC II) were estimated by iBAQ and LFQ methods, in order to evaluate their quantity and abundance. The iBAQ intensities were normalized by dividing each value by that of the major primary scaffoldin ScaA1 in each sample, in order to facilitate interpretation of the results and relate the cellulosomal proteins to the major primary scaffoldin within the samples. The LFQ intensities were normalized by dividing the values by the ScaA1 intensity of CB I in order to simplify the fold-change analysis between the different samples. The table shows 102 identified GH-containing proteins. CB, cellobiose; MCC, microcrystalline cellulose; Doc, dockerin; GH, glycoside hydrolase; CBM, carbohydrate-binding module; CE, carbohydrate esterase; PL, polysaccharide lyases; SLH, S-layer homology module. Significant iBAQ values (≥0.10) are shown in bold