Stoichiometric Assembly of the Cellulosome Generates Maximum Synergy for the Degradation of Crystalline Cellulose, as Revealed by In Vitro Reconstitution of the Clostridium thermocellum Cellulosome

• Published in: Applied and Environmental Microbiology Vol. 81; no. 14; pp. 4756 - 4766
• Main Authors: Hirano, Katsuaki, Nihei, Satoshi, Hasegawa, Hiroki, Haruki, Mitsuru, Hirano, Nobutaka
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.07.2015
• Subjects: Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Cellulases - genetics; Cellulases - metabolism; Cellulose; Cellulose - chemistry; Cellulose - metabolism; Cellulosomes - enzymology; Cellulosomes - genetics; Cellulosomes - metabolism; Chromatography; Clostridium thermocellum; Clostridium thermocellum - enzymology; Clostridium thermocellum - genetics; Clostridium thermocellum - metabolism; Crystallization; Enzymes; Enzymology and Protein Engineering; Gram-positive bacteria; Molecular chemistry; Protein expression; Protein synthesis; Spotlight; Triticum aestivum
• DOI: 10.1128/AEM.00772-15
• ISSN: 0099-2240

The cellulosome is a supramolecular multienzyme complex formed by species-specific interactions between the cohesin modules of scaffoldin proteins and the dockerin modules of a wide variety of polysaccharide-degrading enzymes. Cellulosomal enzymes bound to the scaffoldin protein act synergistically to degrade crystalline cellulose. However, there have been few attempts to reconstitute intact cellulosomes due to the difficulty of heterologously expressing full-length scaffoldin proteins. We describe the synthesis of a full-length scaffoldin protein containing nine cohesin modules, CipA; its deletion derivative containing two cohesin modules, ΔCipA; and three major cellulosomal cellulases, Cel48S, Cel8A, and Cel9K, of the Clostridium thermocellum cellulosome. The proteins were synthesized using a wheat germ cell-free protein synthesis system, and the purified proteins were used to reconstitute cellulosomes. Analysis of the cellulosome assembly using size exclusion chromatography suggested that the dockerin module of the enzymes stoichiometrically bound to the cohesin modules of the scaffoldin protein. The activity profile of the reconstituted cellulosomes indicated that cellulosomes assembled at a CipA/enzyme molar ratio of 1/9 (cohesin/dockerin = 1/1) and showed maximum synergy (4-fold synergy) for the degradation of crystalline substrate and ∼2.4-fold-higher synergy for its degradation than minicellulosomes assembled at a ΔCipA/enzyme molar ratio of 1/2 (cohesin/dockerin = 1/1). These results suggest that the binding of more enzyme molecules on a single scaffoldin protein results in higher synergy for the degradation of crystalline cellulose and that the stoichiometric assembly of the cellulosome, without excess or insufficient enzyme, is crucial for generating maximum synergy for the degradation of crystalline cellulose.