The present invention provides a D-glucaric acid-producing bacterium and a method for producing D-glucaric acid. The present invention is characterized in that D-glucaric acid or a salt thereof is produced from one or more saccharides selected from the group consisting of D-glucose, D-gluconic acid and D-glucuronic acid with catalytic action of a specific alcohol dehydrogenase PQQ-ADH (1) and a specific aldehyde dehydrogenase PQQ-ALDH (2), and that D-glucaric acid or a salt thereof is produced by using a microorganism having the PQQ-ADH (1) and the PQQ-ALDH (2) or a processed product thereof in the presence of the one or more saccharides. The present invention can provide a microorganism having improved productivity of D-glucaric acid to be used for production of D-glucaric acid and a method for efficiently producing D-glucaric acid.

The present invention provides a D-glucaric acid-producing bacterium and a method for producing D-glucaric acid. The present invention is characterized in that D-glucaric acid or a salt thereof is produced from one or more saccharides selected from the group consisting of D-glucose, D-gluconic acid and D-glucuronic acid with catalytic action of a specific alcohol dehydrogenase PQQ-ADH (1) and a specific aldehyde dehydrogenase PQQ-ALDH (2), and that D-glucaric acid or a salt thereof is produced by using a microorganism having the PQQ-ADH (1) and the PQQ-ALDH (2) or a processed product thereof in the presence of the one or more saccharides. The present invention can provide a microorganism having improved productivity of D-glucaric acid to be used for production of D-glucaric acid and a method for efficiently producing D-glucaric acid.

The present invention relates to a field of genetically modified fungal cells and converting galacturonic acid to meso-galactaric acid, more precisely to a method of producing meso-galactaric acid. The invention further relates to recombinant fungal cells having a specific combination of modifications including but not limited to expression of uronate dehydrogenase enzyme, reduced D-galacturonic acid reductase activity, and furthermore reduced meso-galactaric acid catabolism, as well as uses and methods related thereto.

The present invention relates to a field of genetically modified fungal cells and converting galacturonic acid to meso-galactaric acid, more precisely to a method of producing meso-galactaric acid. The invention further relates to recombinant fungal cells having a specific combination of modifications including but not limited to expression of uronate dehydrogenase enzyme, reduced D-galacturonic acid reductase activity, and furthermore reduced meso-galactaric acid catabolism, as well as uses and methods related thereto.

Process for the production of an organic acid from a lignocellulosic feedstock. The process is integrated with a pulp mill and comprises: a) pre-treating a lignocellulosic feedstock with an alkaline liquor from the pulp, thereby obtaining a pretreated cellulosic feed and a black liquor; b) subjecting the pretreated cellulosic feed from step a) to enzymatic hydrolysis, thereby obtaining a saccharide feed; c) subjecting the saccharide feed from step b) to microbial fermentation using calcium oxide from the pulp mill as a neutralising agent, thereby obtaining an organic acid calcium salt; d) treating the organic acid calcium salt with sulfuric acid, thereby obtaining the organic acid; e) optionally isolating lignin from the black liquor obtained in step a), thereby obtaining lignin and weak black liquor; and f) returning the black liquor from step a) and/or the weak black liquor from step e) to the pulp mill chemical recovery process.

Process for the production of an organic acid from a lignocellulosic feedstock. The process is integrated with a pulp mill and comprises: a) pre-treating a lignocellulosic feedstock with an alkaline liquor from the pulp, thereby obtaining a pretreated cellulosic feed and a black liquor; b) subjecting the pretreated cellulosic feed from step a) to enzymatic hydrolysis, thereby obtaining a saccharide feed; c) subjecting the saccharide feed from step b) to microbial fermentation using calcium oxide from the pulp mill as a neutralising agent, thereby obtaining an organic acid calcium salt; d) treating the organic acid calcium salt with sulfuric acid, thereby obtaining the organic acid; e) optionally isolating lignin from the black liquor obtained in step a), thereby obtaining lignin and weak black liquor; and f) returning the black liquor from step a) and/or the weak black liquor from step e) to the pulp mill chemical recovery process.

The present invention relates to a process for the conversion of D-glucose. The process according to the invention comprises a step a) in which part of the D-glucose is enzymatically oxidized to D-gluconic acid (lactone) and a portion of the D-glucose which is essentially equimolar thereto is reduced to D-sorbitol. In addition to D-glucose, D-fructose is also present in the reaction mixture of step a). The process comprises a further step b) in which D-sorbitol formed from the D-glucose in step a) is enzymatically oxidized to D-fructose.

The present invention relates to a process for the conversion of D-glucose. The process according to the invention comprises a step a) in which part of the D-glucose is enzymatically oxidized to D-gluconic acid (lactone) and a portion of the D-glucose which is essentially equimolar thereto is reduced to D-sorbitol. In addition to D-glucose, D-fructose is also present in the reaction mixture of step a). The process comprises a further step b) in which D-sorbitol formed from the D-glucose in step a) is enzymatically oxidized to D-fructose.

The invention relates to a method of producing D-xylonate from D-xylose, which includes converting D-xylose to D-xylonate from a coryneform bacterium in which the activity of the iolR gene is reduced or completely switched off compared with the wild type or a mutation of the wild type, or the iolR gene is completed or partially deleted, as well as to a bacterium for carrying out the method.

The invention relates to a method of producing D-xylonate from D-xylose, which includes converting D-xylose to D-xylonate from a coryneform bacterium in which the activity of the iolR gene is reduced or completely switched off compared with the wild type or a mutation of the wild type, or the iolR gene is completed or partially deleted, as well as to a bacterium for carrying out the method.