http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011021767-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a3a5fcca917003260c614f5baacc148
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-88
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filingDate 2010-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ac0057292e8045a74387e0e50eae4c8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af6d4b586a50da1827a4d69ecb26d760
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publicationDate 2011-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2011021767-A1
titleOfInvention B12-Dependent Dehydratases With Improved Reaction Kinetics
abstract Sequences of B 12 -dependent dehydratases with improved reaction kinetics are presented. Use of these B 12 -dependent dehydratases reduce the rate of the enzyme's suicide inactivation in the presence of glycerol and 1,3-propanediol. The enzymes were created using error-prone PCR and oligonucleotide-directed mutagenesis to target the DhaB1 gene, which encodes the α-subunit of glycerol dehydratase. Mutants with improved reaction kinetics were rapidly identified using high throughput assays.
priorityDate 2002-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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