Novel clostridial cell-surface hemicellulose-binding CBM3 proteins

Almog Hershko Rimon, Oded Livnah, Inna Rozman Grinberg, Lizett Ortiz De Ora, Oren Yaniv, Raphael Lamed, Edward A. Bayer, Felix Frolow, Milana Voronov-Goldman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations


A novel member of the family 3 carbohydrate-binding modules (CBM3s) is encoded by a gene (Cthe_0271) in Clostridium thermocellum which is the most highly expressed gene in the bacterium during its growth on several types of biomass substrates. Surprisingly, CtCBM3-0271 binds to at least two different types of xylan, instead of the common binding of CBM3s to cellulosic substrates. CtCBM3-0271 was crystallized and its three-dimensional structure was solved and refined to a resolution of 1.8 Å. In order to learn more about the role of this type of CBM3, a comparative study with its orthologue from Clostridium clariflavum (encoded by the Clocl_1192 gene) was performed, and the three-dimensional structure of CcCBM3-1192 was determined to 1.6 Å resolution. Carbohydrate binding by CcCBM3-1192 was found to be similar to that by CtCBM3-0271; both exhibited binding to xylan rather than to cellulose. Comparative structural analysis of the two CBM3s provided a clear functional correlation of structure and binding, in which the two CBM3s lack the required number of binding residues in their cellulose-binding strips and thus lack cellulose-binding capabilities. This is an enigma, as CtCBM3-0271 was reported to be a highly expressed protein when the bacterium was grown on cellulose. An additional unexpected finding was that CcCBM3-1192 does not contain the calcium ion that was considered to play a structural stabilizing role in the CBM3 family. Despite the lack of calcium, the five residues that form the calcium-binding site are conserved. The absence of calcium results in conformational changes in two loops of the CcCBM3-1192 structure. In this context, superposition of the non-calcium-binding CcCBM3-1192 with CtCBM3-0271 and other calcium-binding CBM3s reveals a much broader two-loop region in the former compared with CtCBM3-0271.

Original languageAmerican English
Pages (from-to)95-104
Number of pages10
JournalActa Crystallographica Section F:Structural Biology Communications
StatePublished - 1 Apr 2021

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  • CBM
  • Clostridium clariflavum
  • Clostridium thermocellum
  • calcium binding
  • cellulosome
  • crystal structure


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