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      Bioprospecting thermophilic glycosyl hydrolases, from hot springs of Himachal Pradesh, for biomass valorization

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          Abstract

          The harnessing of biocatalysts from extreme environment hot spring niche for biomass conversion is significant and promising owing to the special characteristics of extremozymes attributed by intriguing biogeochemistry and extreme conditions of these environments. Hence, in the present study 38 bacterial isolates obtained from hot springs of Manikaran (~ 95 °C), Kalath (~ 50 °C) and Vasist (~ 65 °C) of Himachal Pradesh were screened for glycosyl hydrolases by in situ enrichment technique using lignocellulosic biomass (LCB). Based on their hydrolytic potential 5 isolates were selected and they were Bacillus tequilensis (VCB1, VCB2 and VSDB4), and B. licheniformis (KBFB2 and KBFB3). Cellulolytic activity assayed by growth under submerged fermentation showed that B. tequilensis VCB1 had maximum FPA activity (3.38 IU ml −1) in 48 h, while B. licheniformis KBFB3 excelled for endoglucanase (EGA of 4.81 IU ml −1 in 24 h) and cellobiase (0.71 IU ml −1 in 48 h) activities. Among all the thermophilic biocatalysts evaluated, highest exoglucanase (0.06 IU ml −1) activity was observed in B. tequilensis VSDB4 while endoglucanase of B. licheniformis KBFB3 showed optimum specific activity at pH 7 and 70 °C. Further, the presence of celS, celB and xlnB genes in the isolates suggest their possible role in biomass conversion. Protein profiling by SDS-PAGE analysis revealed that cellulase isoforms migrated with molecular masses of 75 kDa. The endoglucanase activity of promising strain B. licheniformis KBFB3 was enhanced in the presence of Ca 2+, mercaptoethanol and sodium hypochlorite whereas moderately inhibited by Cu 2+, Zn 2+, urea, SDS and H 2O 2. The results of this study indicate scope for the possible development of novel biocatalysts with multifunctional thermostable glycosyl hydrolases from hot springs for efficient hydrolysis of the complex lignocellulosic biomass into simple sugars and other derived bioproducts leading to biomass valorization.

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          The online version of this article (10.1186/s13568-018-0690-4) contains supplementary material, which is available to authorized users.

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          Most cited references35

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          Toward an aggregated understanding of enzymatic hydrolysis of cellulose: noncomplexed cellulase systems.

          Information pertaining to enzymatic hydrolysis of cellulose by noncomplexed cellulase enzyme systems is reviewed with a particular emphasis on development of aggregated understanding incorporating substrate features in addition to concentration and multiple cellulase components. Topics considered include properties of cellulose, adsorption, cellulose hydrolysis, and quantitative models. A classification scheme is proposed for quantitative models for enzymatic hydrolysis of cellulose based on the number of solubilizing activities and substrate state variables included. We suggest that it is timely to revisit and reinvigorate functional modeling of cellulose hydrolysis, and that this would be highly beneficial if not necessary in order to bring to bear the large volume of information available on cellulase components on the primary applications that motivate interest in the subject. 2004 Wiley Periodicals, Inc.
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            • Article: not found

            Lignocellulosic biomass for bioethanol production: Current perspectives, potential issues and future prospects

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              • Article: not found

              Purification and characterization of cellulase produced by Bacillus amyoliquefaciens DL-3 utilizing rice hull.

              A microorganism hydrolyzing rice hull was isolated from soil and identified as Bacillus amyloliquefaciens by analysis of 16S rDNA and partial sequences of the gyrA gene, and named as B. amyloliquefaciens DL-3. With the analysis of SDS-PAGE, the molecular weight of the purified cellulase was estimated to be 54kDa. The purified cellulase hydrolyzed avicel, caboxymethylcellulose (CMC), cellobiose, beta-glucan and xylan, but not p-Nitrophenyl-beta-D-glucopyranoside (PNPG). Optimum temperature and pH for the CMCase activity of the purified cellulase were found to be 50 degrees C and pH 7.0, respectively. The CMCase activity was inhibited by some metal ions, N-bromosuccinimide and EDTA in the order of Hg(2+)>EDTA>Mn(2+)>N-bromosuccinimide>Ni(2+)>Pb(2+)>Sr(2+)>Co(2+)>K(+). The open reading frame of the cellulase from B. amyloliquefaciens DL-3 was found to encode a protein of 499 amino acids. The deduced amino acid sequence of the cellulase from B. amyloliquefaciens DL-3 showed high identity to cellulases from other Bacillus species, a modular structure containing a catalytic domain of the glycoside hydrolase family 5 (GH5), and a cellulose-binding module type 3 (CBM3).
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                Author and article information

                Contributors
                sugithat@yahoo.com
                sujimicro@gmail.com
                beslinjoshi@gmail.com
                sorokina@catalysis.ru
                oxanap@catalysis.ru
                + 91-8903611294 , usivakumartnau@gmail.com
                Journal
                AMB Express
                AMB Express
                AMB Express
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2191-0855
                15 October 2018
                15 October 2018
                2018
                : 8
                : 168
                Affiliations
                [1 ]ISNI 0000 0001 2155 9899, GRID grid.412906.8, Department of Agricultural Microbiology, , Tamil Nadu Agricultural University, ; Coimbatore, 641003 India
                [2 ]ISNI 0000 0001 2254 1834, GRID grid.415877.8, Boreskov Institute of Catalysis (BIC), Siberian Branch of the Russian Academy of Sciences, ; Novosibirsk, Russia
                Author information
                http://orcid.org/0000-0002-7116-1317
                Article
                690
                10.1186/s13568-018-0690-4
                6188974
                30324223
                b72b57d6-04a5-4187-aea6-1f9f00fe3ff4
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 6 June 2018
                : 26 September 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001407, Department of Biotechnology, Ministry of Science and Technology;
                Award ID: DBT/IC-2/Indo-Russia/2014-16/04
                Award Recipient :
                Categories
                Original Article
                Custom metadata
                © The Author(s) 2018

                Biotechnology
                glycosyl hydrolases,thermophilic,biomass,hot springs
                Biotechnology
                glycosyl hydrolases, thermophilic, biomass, hot springs

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