Cloning, sequencing and expression of the xylanase gene from a Bacillus subtilis strain B10 in Escherichia coli [An article from: Bioresource Technology] Buy on Amazon

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Cloning, sequencing and expression of the xylanase gene from a Bacillus subtilis strain B10 in Escherichia coli [An article from: Bioresource Technology]

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PublisherElsevier
ISBN / ASINB000RR9PRA
ISBN-13978B000RR9PR5
AvailabilityAvailable for download now
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Bioresource Technology, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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Bacillus subtilis strain B10 was isolated for degumming of ramie blast fibers, and a fragment of 642-bp was amplified from chromosomal DNA by using primers directed against the sequence of Bacillus subtilis xylanase gene given in GenBank. The positive clones were screened on the selected LB agar plates supplemented with xylan by Congo-red staining method. The recombinant plasmid from one positive clone was used for further analysis and DNA sequencing. The gene sequence is different from the reported xylanase gene sequence in sites of two base pairs. The recombinant plasmid was expressed in Escherichia coli, and xylanase activity was measured. The xylanase distribution in extracellular, intracellular and periplasmic fractions were about 22.4%, 28.0% and 49.6%, respectively. The xylanase had optimal activity at pH 6.0 and 50^oC.
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