Abstract: The present invention relates to an improved biocatalytic process for producing vanillin from ferulic acid based on a genetically engineered Pseudomonas strains, as well as to said Pseudemonas strains.

Abstract: The present invention relates to the production of heterologous polypeptides in a recombinant bacterial host cell, wherein the bacterial host cell is rendered unable to deactivate the promoter controlling the expression of the heterologous polypeptide in the absence of an inducer.

Abstract: The present invention relates to the production of heterologous polypeptides in a recombinant bacterial host cell, wherein the bacterial host cell is rendered unable to deactivate the promoter controlling the expression of the heterologous polypeptide in the absence of an inducer.

Abstract: The present invention relates to the identification, production and use of thermostable alginate lyase enzymes that can be used to partially degrade alginate to yield oligosaccharides or to give complete degradation of alginate to yield (unsaturated) mono-uronates.

Abstract: The present invention relates to the production of heterologous polypeptides in a recombinant bacterial host cell, wherein the bacterial host cell is rendered inable to deactivate the promoter controlling the expression of the heterologous polypeptide in the absence of an inducer.

Abstract: The present invention relates to an improved biocatalytic process for producing vanillin from ferulic acid based on a genetically engineered Pseudomonas strains, as well as to said Pseudemonas strains.

Abstract: The present invention relates to a vector expressible in a prokaryotic host and a nucleic acid sequence comprising a mannose-inducible promoter of the mannose operon of Bacillus subfiles wherein the vector and nucleic acid sequence, respectively, can be suitably used for transforming a host cell for expression of a heterologous nucleic acid sequence coding a polypeptide in, in particular, high cell density fermentation.

Abstract: The present invention relates to the production of heterologous polypeptides in a recombinant bacterial host cell, wherein the bacterial host cell is rendered inable to deactivate the promoter controlling the expression of the heterologous polypeptide in the absence of an inducer.

Abstract: The present invention relates to a vector expressible in a prokaryotic host and a nucleic acid sequence comprising a mannose-inducible promoter of the mannose operon of Bacillus subfiles wherein the vector and nucleic acid sequence, respectively, can be suitably used for transforming a host cell for expression of a heterologous nucleic acid sequence coding a polypeptide in, in particular, high cell density fermentation.

Abstract: The present invention relates to a fermentation process for culturing a host cell comprising a vector which comprises an inducible promoter of the mannose operon wherein the inducible promoter of the mannose operon controls expression of a nucleic acid sequence encoding for a polypeptide, in particular the present invention relates to the high cell density fermentation of a prokaryotic host cell comprising the inducible promoter of the mannose operon in the production of a polypeptide.

Abstract: The present invention relates to a process for preparing, in particular, enantiomerically enriched L-?-amino acids, in particular those of the general formula (I). In this connection, the process according to the invention uses 2-ketocarboxylic acids which are converted into the desired products using a whole-cell catalyst which comprises an amino acid dehydrogenase and a cofactor-regenerating enzyme.

Abstract: The present invention relates to a process for preparing, in particular, enantiomerically enriched L-?-amino acids, in particular those of the general formula (I). In this connection, the process according to the invention uses 2-ketocarboxylic acids which are converted into the desired products using a whole-cell catalyst which comprises an amino acid dehydrogenase and a cofactor-regenerating enzyme.

Abstract: A movable stuffing machine for producing silage is disclosed wherein the silage is stored on the bottom and is used for filling a tubular film. The stuffing machine comprises a stuffing wall (1) which is disposed perpendicular to the longitudinal direction of the stuffing machine and the direction of stuffing. A driven worm-type compactor is mounted on the stuffing wall (1), is aligned at a right angle from a longitudinal direction of the stuffing machine, is disposed in a horizontal direction, and is embodied as a pronged rotor (3) encompassing conveying prongs (9) which are offset in a helical manner. A feeding device (4) encompassing a metering mechanism (6) is placed upstream of said worm type compactor. The stuffing machine also comprises a roll (7) of silo film, which is mounted thereabove and from which the silo film (30) is directed to the guiding wall through at least one deflection roller (8).

Abstract: A movable stuffing machine for producing silage is disclosed wherein the silage is stored on the bottom and is used for filling a tubular film. The stuffing machine comprises a stuffing wall (1) which is disposed perpendicular to the longitudinal direction of the stuffing machine and the direction of stuffing. The inventive stuffing machine further comprises a driven worm-type compactor that is mounted on the stuffing wall (1), is aligned at a right angle from longitudinal direction of the stuffing machine, is disposed in a horizontal direction, and is embodied as a pronged rotor (3) encompassing conveying prongs (9) which are offset in a helical manner. A feeding device (4) encompassing a metering mechanism (6) is placed upstream of said worm type compactor. The stuffing machine also comprises a roll (7) of silo film, which is mounted there above and from which the silo film (30) is directed to the guiding wall through at least one deflection roller (8).

Abstract: The instant invention is directed to a rec-hydantoin-racemase from Arthrobacter aurescens DSM 3747. Furthermore, the gene encoding for the racemase and plasmids, vectors and microorganisms comprising this gene are to be protected. Use in a process for the production of amino carboxylic acids or derivatives thereof.

Abstract: A novel rec-L-N-carbamoylase from Arthrobacter aurescens and its method of use for producing L-amino acids. The recombinantly produced L-carbamoylase is unexpectedly stable, so that an industrial method of producing L-amino acids can be established with it, in contrast to previously known L-carbamoylases.

Abstract: The present invention relates to a new D-carbamoylase and the gene sequences which code for this from the organism Arthrobacter crystallopoietes DSM 20117. Plasmids, vectors, microorganisms, particular primers and specific possible uses of the enzymes according to the invention are also mentioned. The invention moreover describes a new process for the discovery of enzymes which can be employed in a process for the preparation of D-amino acids starting from 5′-substituted hydantoins.

Abstract: A novel rec-L-N-carbamoylase from Arthrobacter aurescens and its method of use for producing L-amino acids. The recombinantly produced L-carbamoylase is unexpectedly stable, so that an industrial method of producing L-amino acids can be established with it, in contrast to previously known L-carbamoylases.

Abstract: A microorganism is described which is transformed with DNAs which encode a hydantoinnase, a racemase, and a carbamoylase. As a result, the microorganism is able to degrade hydantoins directly to amino acids. A process for the production of the microorganism and a process for producing amino acids with the microorganism is also described.

Abstract: A whole cell catalyst is described comprising a hydantoinase, a racemase and a carbamoylase. Thus this catalyst is able to degrade hydantoins directly into the amino acids.