1993
DOI: 10.1016/0378-1119(93)90372-a
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Cloning and structural organization of a xylanase-encoding gene from Penicillium chrysogenum

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Cited by 39 publications
(28 citation statements)
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“…Initially, only 510 bp of the 5Ј noncoding region of xylP was analyzed (18). In order to characterize the complete 1,676-bp promoter fragment employed for overexpression of nreB (21), the region between an SalI site and the xylP translation start codon was sequenced in its entirety and was analyzed to determine the presence of putative transcription factor binding sites.…”
Section: Resultsmentioning
confidence: 99%
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“…Initially, only 510 bp of the 5Ј noncoding region of xylP was analyzed (18). In order to characterize the complete 1,676-bp promoter fragment employed for overexpression of nreB (21), the region between an SalI site and the xylP translation start codon was sequenced in its entirety and was analyzed to determine the presence of putative transcription factor binding sites.…”
Section: Resultsmentioning
confidence: 99%
“…cesses like paper pulp bleaching or bioconversion of biomass into fuels and chemicals (31 (12,18,25,28,35,45,48,53,54).…”
Section: Discussionmentioning
confidence: 99%
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“… îñòàíí³ äåê³ëüêà ðîê³â çíà÷íèé ïðîгðåñ áóâ äîñÿгíóòèé â êëîíóâàíí³ ðÿäó êñèëàíîë³òè÷íèõ гåí³â ó òàêèõ гðèá³â ÿê Aspergillus swamori [29], A. nidulans [31,43], A. oryzae [32], A. niger [33], Chaetomium gracile [60], Penicillium chrysogenum [27], Trichoderma viride [56]. Êð³ì êñèëàíîë³òè÷íèõ гåí³â, ç àñïåðг³ëë³â òà T. reesi áóëî ³çîëüîâàíî áàгàòî гåí³â, ÿê³ êîäóþòü äîïîì³жí³ фåðìåíòè, òàê³ ÿê àöåòèëêñèëàí åñòåðàçà [24], [37], α L àðàá³íîфóðàíîç³äàçà [21], àðàá³íîêñèëàí àðàá³íîфóðàíîçèäàçà [22], α гëþêóðîí³äàçà [58], фåðóî³ë åñòåðàçà [57].…”
Section: продукція ксиланазиunclassified