Toggle Main Menu Toggle Search

Open Access padlockePrints

A family 26 mannanase produced by Clostridium thermocellum as a component of the cellulosome contains a domain which is conserved in mannanases from anaerobic fungi

Lookup NU author(s): Emeritus Professor Harry Gilbert

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

Cellulosomes prepared by the cellulose affinity digestion method from clostridium thermocellum culture supernatant hydrolysed carob galactomannan during incubation at 60°C and pH 6.5. A recombinant phage expressing mannanase activity was isolated from a library of C. thermocellum genomic DNA constructed in λZAPII. The cloned fragment of DNA containing a putative mannanase gene (manA) was sequenced, revealing an ORF of 1767 nt, encoding a protein (mannanase A; Man26A) of 589 aa with a molecular mass of 66816 Da. The putative catalytic domain (CD) of Man26A, identified by gene sectioning and sequence comparisons, displayed up to 32% identity with other mannanases belonging to family 26. Immediately downstream of the CD and separated from it by a short proline/threonine linker was a duplicated 24-residue dockerin motif, which is conserved in all C. thermocellum cellulosomal enzymes described thus far and mediates their attachment to the cellulosome-integrating protein (CipA). Man26A consisting of the CD alone (Man26A') was hyperexpressed in Escherichia coli BL21(DE3) and purified. The truncated enzyme hydrolysed soluble and insoluble mannan, displaying a temperature optimum of 65°C and a pH optimum of 6.5, but exhibited no activity against other plant cell wall polysaccharides. Antiserum raised against Man26A' cross-reacted with a polypeptide with a molecular mass of 70,000 Da that is part of the C. thermocellum cellulosome. A second variant of Man26A containing the N-terminal segment of 130 residues and the CD (Man26A') bound to ivory-nut mannan and weakly to soluble Carob galactomannan and insoluble cellulose. Man26A' consisting of the CD alone did not bind to these polysaccharides. These results indicate that the N-terminal 130 residues of mature Man26A may constitute a weak mannan-binding domain. Sequence comparisons revealed a lack of identity between this region of Man26A and other polysaccharide-binding domains, but significant identity with a region conserved in the three family 26 mannanases from the anaerobic fungus Piromyces equi.


Publication metadata

Author(s): Halstead JR, Vercoe PE, Gilbert HJ, Davidson K, Hazlewood GP

Publication type: Article

Publication status: Published

Journal: Microbiology

Year: 1999

Volume: 145

Issue: 11

Pages: 3101-3108

Print publication date: 01/11/1999

ISSN (print): 13500872

ISSN (electronic): 1465-2080

Publisher: Society for General Microbiology

URL: http://mic.sgmjournals.org/content/145/11/3101.long

PubMed id: 10589717


Share