Patents by Inventor Doerte ROTHER

Doerte ROTHER has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 10465211
    Abstract: A lyase has an amino acid sequence selected from SEQ ID NOs: 1, 2 and 3, wherein the amino acid isoleucine in position no. 468 in the protein ApPDC-E469G, which is modified with respect to the wild type from Acetobacter pasteurianus, is replaced by an amino acid which occupies less space than isoleucine.
    Type: Grant
    Filed: August 27, 2015
    Date of Patent: November 5, 2019
    Assignee: FORSCHUNGSZENTRUM JUELICH GMBH
    Inventors: Doerte Rother, Martina Pohl, Torsten Sehl, Lisa Marx, Robert Westphal
  • Patent number: 10006061
    Abstract: The invention relates to a lyase and a lyase-encoding DNA, to vectors containing the DNA and to a method for the asymmetric synthesis of (S)-phenylacetylcarbinol. According to the invention, a lyase is provided, in which tryptophan is replaced with an amino acid at position 543 in protein ApPDC-E469G, said protein being modified with respect to the wild type of Aceobacter pasteurianus, or in which it is less space-filling than tryptophan. According to the invention, deoxyribonucleic acids are furthermore provided, which encode the lyase. (S)-phenylacetylcarbinol can be produced with the lyase according to the invention from the educts benzaldehyde and pyruvate or acetaldehyde with an enantiomeric excess of at least 94%.
    Type: Grant
    Filed: August 14, 2015
    Date of Patent: June 26, 2018
    Assignee: FORSCHUNGSZENTRUM JUELICH GMBH
    Inventors: Doerte Rother, Martina Pohl, Torsten Sehl, Lisa Marx, Robert Westphal
  • Patent number: 9890406
    Abstract: A method for producing cathine ((1S,2S)-norpseudoephedrine), in which, in a first reaction step, benzaldehyde is reacted with an acetyl donor according to formula (1), where R?H or COOH, by way of an (S)-selective lease to yield an enantiomer mixture according to formulas (2) and (3) and, in a second step, the compound according to formula (3) is reacted with an amine donor by way of an (S)-selective transaminase to yield (1S,2S)-norpseudoephedrine.
    Type: Grant
    Filed: May 17, 2014
    Date of Patent: February 13, 2018
    Assignee: Forschungszentrum Juelich GmbH
    Inventors: Doerte Rother, Martina Pohl, Torsten Sehl, Alvaro Gomez Baraibar
  • Publication number: 20170260550
    Abstract: A lyase has an amino acid sequence selected from SEQ ID NOs: 1, 2 and 3, wherein the amino acid isoleucine in position no. 468 in the protein ApPDC-E469G, which is modified with respect to the wild type from Acetobacter pasteurianus, is replaced by an amino acid which occupies less space than isoleucine.
    Type: Application
    Filed: August 27, 2015
    Publication date: September 14, 2017
    Applicant: Forschungszentrum Juelich GmbH
    Inventors: Doerte Rother, Martina Pohl, Torsten Sehl, Lisa Marx, Robert Westphal
  • Publication number: 20170253894
    Abstract: The invention relates to a lyase and a lyase-encoding DNA, to vectors containing the DNA and to a method for the asymmetric synthesis of (S)-phenylacetylcarbinol. According to the invention, a lyase is provided, in which tryptophan is replaced with an amino acid at position 543 in protein ApPDC-E469G, said protein being modified with respect to the wild type of Aceobacter pasteurianus, or in which it is less space-filling than tryptophan. According to the invention, deoxyribonucleic acids are furthermore provided, which encode the lyase. (S)-phenylacetylcarbinol can be produced with the lyase according to the invention from the educts benzaldehyde and pyruvate or acetaldehyde with an enantiomeric excess of at least 94%.
    Type: Application
    Filed: August 14, 2015
    Publication date: September 7, 2017
    Inventors: Doerte Rother, Martina Pohl, Torsten Sehl, Lisa Marx, Robert Westphal
  • Publication number: 20160138062
    Abstract: A method for producing cathine ((1S,2S)-norpseudoephedrine), in which, in a first reaction step, benzaldehyde is reacted with an acetyl donor according to formula (1), where R?H or COOH, by way of an (S)-selective lease to yield an enantiomer mixture according to formulas (2) and (3) and, in a second step, the compound according to formula (3) is reacted with an amine donor by way of an (S)-selective transaminase to yield (1S,2S)-norpseudoephedrine.
    Type: Application
    Filed: May 17, 2014
    Publication date: May 19, 2016
    Inventors: Doerte ROTHER, Martina POHL, Torsten SEHL, Alvaro Gomez BARAIBAR