Abstract:
:The cyclomaltodextrinase gene from Bacillus subtilis high-temperature growth transformant H-17 was cloned on separate PstI, BamHI, and EcoRI fragments into the plasmid vector pUC18, but was expressed in an inactive form in the host, Escherichia coli DH5 alpha. High level constitutive expression of the gene product was also detrimental to the E. coli host, which led to structural instability of the recombinant plasmid. The cyclomaltodextrinase gene was cloned on a 3-kb EcoRI fragment into the plasmid vector pPL708, and the fragment was structurally maintained in the host B. subtilis YB886. The cloned gene product was synthesized in an enzymatically active form in the B. subtilis host; however, expression was at a low level. Subcloning of the 3-kb EcoRI fragment into pUC18 and transformation into E. coli XL1-Blue (F' lacIq) indicated that the cyclomaltodextrinase gene was cloned with its own promoter, since expression of the gene occurred in the absence of IPTG. Subcloning of the cyclomaltodextrinase gene downstream from the Bacillus temperature phage SPO2 promoter of pPL708 may increase expression of this gene.
journal_name
Curr Microbioljournal_title
Current microbiologyauthors
Krohn BM,Lindsay JAdoi
10.1007/BF01577379subject
Has Abstractpub_date
1993-04-01 00:00:00pages
217-22issue
4eissn
0343-8651issn
1432-0991journal_volume
26pub_type
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journal_title:Current microbiology
pub_type: 杂志文章
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journal_title:Current microbiology
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pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Current microbiology
pub_type: 杂志文章
doi:10.1007/BF00298381
更新日期:1995-10-01 00:00:00
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journal_title:Current microbiology
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journal_title:Current microbiology
pub_type: 杂志文章
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journal_title:Current microbiology
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