Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker

Non-cellulosomal processive endoglucanase 9I (Cel9I) from Clostridium thermocellum is a modular protein, consisting of a family-9 glycoside hydrolase (GH9) catalytic module and two family-3 carbohydrate-binding modules (CBM3c and CBM3b), separated by linker regions. GH9 does not show cellulase activ...

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Main Authors: Svetlana Petkun, Inna Rozman Grinberg, Raphael Lamed, Sadanari Jindou, Tal Burstein, Oren Yaniv, Yuval Shoham, Linda J.W. Shimon, Edward A. Bayer, Felix Frolow
Format: Article
Language:English
Published: PeerJ Inc. 2015-09-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/1126.pdf
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spelling doaj-26351109aec3429e8564b6eb536ca6982020-11-24T22:33:44ZengPeerJ Inc.PeerJ2167-83592015-09-013e112610.7717/peerj.1126Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linkerSvetlana Petkun0Inna Rozman Grinberg1Raphael Lamed2Sadanari Jindou3Tal Burstein4Oren Yaniv5Yuval Shoham6Linda J.W. Shimon7Edward A. Bayer8Felix Frolow9Department of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelDepartment of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelDepartment of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelDepartment of Life Sciences, Meijo University, Nagoya, JapanDepartment of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelDepartment of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelDepartment of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa, IsraelDepartment of Chemical Research Support, The Weizmann Institute of Science, Rehovot, IsraelDepartment of Biological Chemistry, The Weizmann Institute of Science, Rehovot, IsraelDepartment of Molecular Microbiology and Biotechnology, The Daniella Rich Institute for Structural Biology, Tel Aviv University, Ramat Aviv, IsraelNon-cellulosomal processive endoglucanase 9I (Cel9I) from Clostridium thermocellum is a modular protein, consisting of a family-9 glycoside hydrolase (GH9) catalytic module and two family-3 carbohydrate-binding modules (CBM3c and CBM3b), separated by linker regions. GH9 does not show cellulase activity when expressed without CBM3c and CBM3b and the presence of the CBM3c was previously shown to be essential for endoglucanase activity. Physical reassociation of independently expressed GH9 and CBM3c modules (containing linker sequences) restored 60–70% of the intact Cel9I endocellulase activity. However, the mechanism responsible for recovery of activity remained unclear. In this work we independently expressed recombinant GH9 and CBM3c with and without their interconnecting linker in Escherichia coli. We crystallized and determined the molecular structure of the GH9/linker-CBM3c heterodimer at a resolution of 1.68 Å to understand the functional and structural importance of the mutual spatial orientation of the modules and the role of the interconnecting linker during their re-association. Enzyme activity assays and isothermal titration calorimetry were performed to study and compare the effect of the linker on the re-association. The results indicated that reassembly of the modules could also occur without the linker, albeit with only very low recovery of endoglucanase activity. We propose that the linker regions in the GH9/CBM3c endoglucanases are important for spatial organization and fixation of the modules into functional enzymes.https://peerj.com/articles/1126.pdfFamily-9 glycoside hydrolaseClostridium thermocellumProtein–protein interactionX-ray structureCarbohydrate-binding module (CBM)
collection DOAJ
language English
format Article
sources DOAJ
author Svetlana Petkun
Inna Rozman Grinberg
Raphael Lamed
Sadanari Jindou
Tal Burstein
Oren Yaniv
Yuval Shoham
Linda J.W. Shimon
Edward A. Bayer
Felix Frolow
spellingShingle Svetlana Petkun
Inna Rozman Grinberg
Raphael Lamed
Sadanari Jindou
Tal Burstein
Oren Yaniv
Yuval Shoham
Linda J.W. Shimon
Edward A. Bayer
Felix Frolow
Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
PeerJ
Family-9 glycoside hydrolase
Clostridium thermocellum
Protein–protein interaction
X-ray structure
Carbohydrate-binding module (CBM)
author_facet Svetlana Petkun
Inna Rozman Grinberg
Raphael Lamed
Sadanari Jindou
Tal Burstein
Oren Yaniv
Yuval Shoham
Linda J.W. Shimon
Edward A. Bayer
Felix Frolow
author_sort Svetlana Petkun
title Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
title_short Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
title_full Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
title_fullStr Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
title_full_unstemmed Reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
title_sort reassembly and co-crystallization of a family 9 processive endoglucanase from its component parts: structural and functional significance of the intermodular linker
publisher PeerJ Inc.
series PeerJ
issn 2167-8359
publishDate 2015-09-01
description Non-cellulosomal processive endoglucanase 9I (Cel9I) from Clostridium thermocellum is a modular protein, consisting of a family-9 glycoside hydrolase (GH9) catalytic module and two family-3 carbohydrate-binding modules (CBM3c and CBM3b), separated by linker regions. GH9 does not show cellulase activity when expressed without CBM3c and CBM3b and the presence of the CBM3c was previously shown to be essential for endoglucanase activity. Physical reassociation of independently expressed GH9 and CBM3c modules (containing linker sequences) restored 60–70% of the intact Cel9I endocellulase activity. However, the mechanism responsible for recovery of activity remained unclear. In this work we independently expressed recombinant GH9 and CBM3c with and without their interconnecting linker in Escherichia coli. We crystallized and determined the molecular structure of the GH9/linker-CBM3c heterodimer at a resolution of 1.68 Å to understand the functional and structural importance of the mutual spatial orientation of the modules and the role of the interconnecting linker during their re-association. Enzyme activity assays and isothermal titration calorimetry were performed to study and compare the effect of the linker on the re-association. The results indicated that reassembly of the modules could also occur without the linker, albeit with only very low recovery of endoglucanase activity. We propose that the linker regions in the GH9/CBM3c endoglucanases are important for spatial organization and fixation of the modules into functional enzymes.
topic Family-9 glycoside hydrolase
Clostridium thermocellum
Protein–protein interaction
X-ray structure
Carbohydrate-binding module (CBM)
url https://peerj.com/articles/1126.pdf
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