Michel Chartrain - Westfield NJ, US Laura Kizer Bentley - Monmouth NJ, US Barbara Ann Krulewicz - Bloomfield NJ, US Kristin M. Listner - East Windsor NJ, US Wen-jun Sun - Edison NJ, US Chanyong Brian Lee - Thousand Oaks CA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C12N 15/63 C12N 1/21 C12N 15/70
US Classification:
4353201, 4352523, 435471
Abstract:
The present invention relates generally to a method for increasing the yield of plasmid DNA production. The method includes the steps of selecting a highly productive clonal subtype of a strain of , including but not limited to the DH5 strain, harboring a DNA plasmid and cultivating said clonal subtype with fed-batch fermentation in a chemically-defined medium. The plasmid DNA production process described herein can generate record quantities of plasmid DNA when said highly productive clonal subtypes are cultivated on an industrial scale. The disclosed method can be used for the production of pharmaceutical grade DNA for use in polynucleotide vaccination and gene therapy treatment regimens.
Process For Large Scale Production Of Plasmid Dna By Fermentation
Michel Chartrain - Westfield NJ, US Laura Kizer Bentley - Monmouth NJ, US Barbara Ann Krulewicz - Bloomfield NJ, US Kristin M. Listner - East Windsor NJ, US Wen-jun Sun - Edison NJ, US Chanyong Brian Lee - Thousand Oaks CA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C12N 1/20 C12N 15/63
US Classification:
43525233, 4353201
Abstract:
The present invention relates generally to a method for increasing the yield of plasmid DNA production. The method includes the steps of selecting a highly productive clonal subtype of a strain of , including but not limited to the DH5 strain, harboring a DNA plasmid and cultivating said clonal subtype with fed-batch fermentation in a chemically-defined medium. The plasmid DNA production process described herein can generate record quantities of plasmid DNA when said highly productive clonal subtypes are cultivated on an industrial scale. The disclosed method can be used for the production of pharmaceutical grade DNA for use in polynucleotide vaccination and gene therapy treatment regimens.
Asymmetric Bioreduction Of 6-Bromo-2-Tetralone To (S)-6-Bromo-2 Tetraol By Trichosporon Capitatum
Michel M. Chartrain - Westfield NJ Jayanthi Reddy - Scotch Plains NJ David M. Tschaen - Holmdel NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C12P 722 C12P 4100
US Classification:
435156
Abstract:
Stereospecific (S)-6-bromo-2-tetraol is a key intermediate in the chemical synthesis of the chiral drug candidate, MK499, a ventricular arrythmias suppressant. The yeast strain Trichosporon capitatum (MY 1890) was employed for the bioconversion of 6-bromo-2-tetralone to the corresponding alcohol.
Michel M. Chartrain - Westfield NJ George M. Garrity - Westfield NJ Brian Heimbuch - North Brunswick NJ Christopher Roberge - Clark NJ Ali Shafiee - Westfield NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C12P 1716 C12P 1712
US Classification:
435118
Abstract:
The present invention provides a process for the stereoselective reduction of phenylalkyl ketones to their corresponding (S)-hydroxy compounds. The process utilizes the novel microorganism Microbacterium MB 5614 to effectuate the chiral reduction. The present invention also provides said novel Microbacterium, which has been deposited with the ATCC and assigned the accession number ATCC 55557.
Quantitative Conversion Of Indene To (1S,2R) Indene Oxide And (1S,2R)-Indandiol By Combination Of Haloperoxidase Bioconversion And Chemical Steps
Michel M. Chartrain - Westfield NJ Neal C. Connors - Fanwood NJ George M. Garrity - Westfield NJ Roger C. Olewinski - Milltown NJ Thomas R. Verhoeven - Cranford NJ Jinyou Zhang - Edison NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C12P 1702 C12P 722 C12P 102 C12P 500
US Classification:
435123
Abstract:
A process is disclosed that quantitatively bioconverts indene to (1S,2R)-indene oxide and (1S,2R)-indandiol, by the action of fungal haloperoxidase followed by various chemical step(s), e. g. , adjusting the pH.
Stereospecific Bioconversion Of Benzyl Acetoacetate To Benzyl-(S)-(+)-Hydroxybutyrate
Michel M. Chartrain - Westfield NJ Barbara A. Krulewicz - Bloomfield NJ Paul N. Devine - Lincroft NJ David M. Tschaen - Holmdel NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C12P 700 C07D31744
US Classification:
435132
Abstract:
The invention relates to a class of enantiomerically pure intermediates represented by Formula I, where X is F, Cl, Br, or I, and a novel enantioselective bioreductive process using yeast to form these intermediates, which are useful in the synthesis of endothelin antagonists, and the like. ##STR1##.
Resolution Of Racemic Indene Oxide To Yield (1S,2R)-Indene Oxide Using Diplodia Gossipina
Michel M. Chartrain - Westfield NJ Chris H. Senanayake - North Brunswick NJ Jinyou Zhang - Edison NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C12P 1702 C12P 4100
US Classification:
435280
Abstract:
A process is disclosed that hydrolyzes, by the action of an epoxide hydrolase of Diplodia gossipina (alternatively named Diplodia gossypina) ATCC 16391 or ATCC 10936, the undesired enantiomer of racemic indene oxide, an epoxide of indan.
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