Please use this identifier to cite or link to this item:
https://hdl.handle.net/10321/1649
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhang, Meng | en_US |
dc.contributor.author | Puri, Adarsh Kumar | en_US |
dc.contributor.author | Govender, Algasan | en_US |
dc.contributor.author | Wang, Zheng-Xiang | en_US |
dc.contributor.author | Singh, Suren | en_US |
dc.contributor.author | Perumal, Kugenthiren | en_US |
dc.date.accessioned | 2016-10-13T06:01:41Z | - |
dc.date.available | 2016-10-13T06:01:41Z | - |
dc.date.issued | 2014-12-03 | - |
dc.identifier.citation | Zhang, M. et al. 2014. The multi-chitinolytic enzyme system of the compost-dwelling thermophilic fungus Thermomyces lanuginosus. Process Biochemistry. Vol 50 : 237-244 | en_US |
dc.identifier.issn | 1359-5113 | - |
dc.identifier.uri | http://hdl.handle.net/10321/1649 | - |
dc.description.abstract | The recent sequencing of the Thermomyces lanuginosus SSBP genome by our group has revealed four putative family 18 chitinases. In this study, three novel chitinase genes (chit2, chit3 and chit4) and the previously-reported chit1 gene were cloned from T. lanuginosus SSBP. chit1, encoding a 44.1 kDa protein, and chit2, encoding a 36.6 kDa protein, were successfully expressed in Pichia pastoris. The recombinant Chit1 and Chit2 enzymes exhibited optimum activity at pH 5.0 and pH 4.0, respectively. Chit1 had optimal activity at 50 ◦C and retained 56% of its activity at 60 ◦C after 30 min, while Chit2 was optimally active at 40 ◦C and retained 71% of its activity at 50 ◦C after 60 min. Both enzymes produced chitobiose as the major product using different substrates. Chit2 displayed antifungal activity against Penicillium verrucosum and Aspergillus niger. These activities could be useful in the environmental degradation of chitinous wastes as well as for biotechnological applications. | en_US |
dc.format.extent | 8 p | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Process biochemistry (1991) | - |
dc.subject | Chitin | en_US |
dc.subject | Chitro-oligosaccarides | en_US |
dc.subject | Thermomyces lanuginosus SSBP | en_US |
dc.subject | Exo/endochitinases | en_US |
dc.subject | Crude shrimp shell powder | en_US |
dc.title | The multi-chitinolytic enzyme system of the compost-dwelling thermophilic fungus Thermomyces lanuginosus | en_US |
dc.type | Article | en_US |
dc.publisher.uri | http://ac.els-cdn.com/S1359511314005868/1-s2.0-S1359511314005868-main.pdf?_tid=20ce4c62-9053-11e6-8989-00000aab0f26&acdnat=1476259918_dcd6133593501863e1f748d665cf29aa | en_US |
dc.dut-rims.pubnum | DUT-005188 | en_US |
dc.description.availability | Copyright: 2014.Elsevier. Due to copyright restrictions, only the abstract is available. For access to the full text item, please consult the publisher's website. The definitive version of the work is published in African Journal for Process Biochemistry, Process Biochemistry Vol 50, No 1, pp 234-244 | en_US |
dc.identifier.doi | 10.1016/j.procbio.2014.11.008 | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
Appears in Collections: | Research Publications (Applied Sciences) |
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