Mannan endo-1,4-β-mannosidase from Kitasatospora sp. isolated in Indonesia and its potential for production of mannooligosaccharides from mannan polymers
Nanik Rahmani,
Norimasa Kashiwagi,
JaeMin Lee,
Satoko Niimi-Nakamura,
Hana Matsumoto,
Prihardi Kahar,
Puspita Lisdiyanti,
Yopi,
Bambang Prasetya,
Chiaki Ogino,
Akihiko Kondo
Affiliations
Nanik Rahmani
Research Center for Biotechnology, Indonesian Institute of Sciences, Komplek CSC-LIPI
Norimasa Kashiwagi
Graduate School of Science, Technology and Innovation, Kobe University
JaeMin Lee
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
Satoko Niimi-Nakamura
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
Hana Matsumoto
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
Prihardi Kahar
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
Puspita Lisdiyanti
Research Center for Biotechnology, Indonesian Institute of Sciences, Komplek CSC-LIPI
Yopi
Research Center for Biotechnology, Indonesian Institute of Sciences, Komplek CSC-LIPI
Bambang Prasetya
Research Center for Biotechnology, Indonesian Institute of Sciences, Komplek CSC-LIPI
Chiaki Ogino
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
Akihiko Kondo
Graduate School of Science, Technology and Innovation, Kobe University
Abstract Mannan endo-1,4-β-mannosidase (commonly known as β-mannanase) catalyzes a random cleavage of the β-d-1,4-mannopyranosyl linkage in mannan polymers. The enzyme has been utilized in biofuel production from lignocellulose biomass, as well as in production of mannooligosaccharides (MOS) for applications in feed and food industries. We aimed to obtain a β-mannanase, for such mannan polymer utilization, from actinomycetes strains isolated in Indonesia. Strains exhibiting high mannanase activity were screened, and one strain belonging to the genus Kitasatospora was selected. We obtained a β-mannanase from this strain, and an amino acid sequence of this Kitasatospora β-mannanase showed a 58–71% similarity with the amino acid sequences of Streptomyces β-mannanases. The Kitasatospora β-mannanase showed a significant level of activity (944 U/mg) against locust bean gum (0.5% w/v) and a potential for oligosaccharide production from various mannan polymers. The β-mannanase might be beneficial particularly in the enzymatic production of MOS for applications of mannan utilization.