Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/69789
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dc.contributor.authorLee, Y.C.en_US
dc.contributor.authorChien, H.C.R.en_US
dc.contributor.authorHsu, W.H.en_US
dc.date2007zh_TW
dc.date.accessioned2014-06-11T05:58:54Z-
dc.date.available2014-06-11T05:58:54Z-
dc.identifier.issn0168-1656zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/69789-
dc.description.abstractN-acetyl-D-neuraminic acid (NeuAc; sialic acid) is a precursor for the manufacture of many pharmaceutical drugs, such as anti-influenza virus agents. To develop a whole cell process for NeuAc production, genes of Anabaena sp. CH1 N-acetyl-D-glucosamine 2-epimerase (bage) and Escherichia coli N-acetyl-D-neuraminic acid lyase (nanA) were cloned and expressed in E. coli BL21 (DE3). The expressed bGlcNAc 2-epimerase was purified from the crude cell extract of IPTG-induced E. coli BL21 (DE3) (pET-bage) to homogeneity by nickel-chelate chromatography. The molecular mass of the purified bGlcNAc 2-epimerase was determined to be 42 kDa by SIDS-PAGE. The pH and temperature optima of the recombinant bGlcNAc 2-epimerase were pH 7.0 and 50 degrees C, respectively, and only needs 20 mu m ATP for maximal activity. The specific activity of bGlcNAc 2-epimerase (124U mg(-1) protein) for the conversion of N-acetyl-D-glucosamine to N-acetyl-D-manosamine was about four-fold higher than that of porcine N-acetyl-D-glucosamine 2-epimerase. A stirred glass vessel containing transformed E. coli cells expressing age gene from Anabaena sp. CH1 and NeuAc lyase gene from E. coli NovaBlue separately was used for the conversion of GlcNAc and pyruvate to NeuAc. A maximal productivity of 10.2 g NeuAc l(-1) h(-1) with 33.3% conversion yield from GlcNAc could be obtained in a 12-h reaction. The recombinant E. coli cells can be reused for more than eight cycles with a productivity of > 8.0 g NeuAc L-1 h(-1). In this process, the expensive activator, ATP, necessary for maximal activity of GlcNAc 2-epimerase in free enzyme system can be omitted. (c) 2007 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USzh_TW
dc.relationJournal of Biotechnologyen_US
dc.relation.ispartofseriesJournal of Biotechnology, Volume 129, Issue 3, Page(s) 453-460.en_US
dc.relation.urihttp://dx.doi.org/10.1016/j.jbiotec.2007.01.027en_US
dc.subjectN-acetyl-D-glucosamine 2-epimeraseen_US
dc.subjectN-acetyl-D-neuraminic acid lyaseen_US
dc.subjectsialic acid productionen_US
dc.subjectepimerizationen_US
dc.subjectAnabaena sp.en_US
dc.subjectd-glucosamine 2-epimeraseen_US
dc.subjectrenin-binding-proteinen_US
dc.subjectsialic-aciden_US
dc.subjectacetylneuraminic aciden_US
dc.subjectporcine kidneyen_US
dc.subjectglcnac 2-epimeraseen_US
dc.subjectmolecular-cloningen_US
dc.subjectidentificationen_US
dc.subjectpurificationen_US
dc.subjectmotifen_US
dc.titleProduction of N-acetyl-D-neuraminic acid by recombinant whole cells expressing Anabaena sp CH1N-acetyl-D-glucosamine 2-epimerase and Escherichia coli N-acetyl-D-neuraminic acid lyaseen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1016/j.jbiotec.2007.01.027zh_TW
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