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dc.contributor.authorKim, Eun Sook-
dc.contributor.authorKim, Byeong-Soo-
dc.contributor.authorKim, Ki-Yeon-
dc.contributor.authorWoo, Han-Min-
dc.contributor.authorLee, Sun-Mi-
dc.contributor.authorUm, Youngsoon-
dc.date.accessioned2024-01-19T23:32:04Z-
dc.date.available2024-01-19T23:32:04Z-
dc.date.created2021-09-03-
dc.date.issued2018-02-
dc.identifier.issn0168-1656-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121750-
dc.description.abstractFor cost-effective lignocellulosic biofuel/chemical production, consolidated bioprocessing (CBP)-enabling microorganisms utilizing cellulose as well as producing biofuel/chemical are required. A novel strain Paenibacillus sp. CAA11 isolated from sediment was found to be not only as a cellulose degrader under both aerobic and strict anaerobic conditions but also as a producer of cellulosic biofuel/chemicals. Paenibacillus sp. CAA11 secreted cellulolytic enzymes by its own secretion system and produced ethanol as well as short-chain organic acids (formic acid, acetic acid, lactic acid) from cellulose. Cellulolytic activity of the strain was significantly enhanced by expressing a heterologous endoglucanase 168Cel5 from Bacillus subtilis under both aerobic and anaerobic conditions. The strain harboring the 168cel5 gene revealed 2-fold bigger halo zone on Congo-red plate and 1.75-fold more aerobic cellulose utilization in liquid medium compared with the negative control. Notably, under anaerobic conditions, the recombinant strain expressing 168Cel5 consumed 1.83-fold more cellulose (5.10 g/L) and produced 5-fold more ethanol (0.65 g/L) along with 5-fold more total acids (1.6 g/L) compared with the control, resulting 2.73-fold higher yields. This result demonstrates the potential of Paenibacillus sp. CAA11 as a suitable aerobic and anaerobic CBP-enabling microbe with cellulolytic production of ethanol and short-chain organic acids.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleAerobic and anaerobic cellulose utilization by Paenibacillus sp CAA11 and enhancement of its cellulolytic ability by expressing a heterologous endoglucanase-
dc.typeArticle-
dc.identifier.doi10.1016/j.jbiotec.2018.01.007-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of Biotechnology, v.268, pp.21 - 27-
dc.citation.titleJournal of Biotechnology-
dc.citation.volume268-
dc.citation.startPage21-
dc.citation.endPage27-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000425715100004-
dc.identifier.scopusid2-s2.0-85041317542-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusCURDLANOLYTICUS STRAIN B-6-
dc.subject.keywordPlusCLOSTRIDIUM-CELLULOLYTICUM-
dc.subject.keywordPlusETHANOL-PRODUCTION-
dc.subject.keywordPlusZYMOMONAS-MOBILIS-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusSACCHARIFICATION-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordPlusFERMENTATION-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordAuthorCellulose-
dc.subject.keywordAuthorPaenibacillus-
dc.subject.keywordAuthorConsolidated bioprocessing-
dc.subject.keywordAuthorEndoglucanase-
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KIST Article > 2018
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