Yeast cells having a reductive TCA pathway from pyruvate or phosphoenolpyruvate to succinate, and which include at least one exogenous gene overexpressing an enzyme in that pathway, further contain an exogenous transhydrogenase gene.

Yeast cells having a reductive TCA pathway from pyruvate or phosphoenolpyruvate to succinate, and which include at least one exogenous gene overexpressing an enzyme in that pathway, further contain an exogenous transhydrogenase gene.

Provided is a feed ingredient comprising propionate and a byproduct of fermentation of a feedstock by propionic acid-producing bacteria, wherein said feedstock comprises a carbon source and wherein said bacteria are of a class selected from the group consisting of Actinobacteria, Bacteroidia, Clostridia, Negativicutes and combinations thereof. Also provided are methods for manufacturing the feed ingredient and uses thereof.

Provided is a feed ingredient comprising propionate and a byproduct of fermentation of a feedstock by propionic acid-producing bacteria, wherein said feedstock comprises a carbon source and wherein said bacteria are of a class selected from the group consisting of Actinobacteria, Bacteroidia, Clostridia, Negativicutes and combinations thereof. Also provided are methods for manufacturing the feed ingredient and uses thereof.

The present disclosure provides thiolases and polypeptide variants of 3-hydroxybutyryl-CoA dehydrogenase, nucleic acids encoding the same, vectors comprising the nucleic acids, and cells comprising the polypeptide variants and/or thiolase, the nucleic acids, and/or the vectors. The present disclosure also provides methods of making and using the same, including methods for culturing cells, and for the production of various products, including 3-hydroxybutyryl-CoA (3-HB-CoA), 3-hydroxybutyraldehyde (3-HBal), 3-hydroxybutyrate (3-HB), 1,3-butanediol (1,3-BDO), and esters and amides thereof, and products made from any of these.

The present disclosure provides thiolases and polypeptide variants of 3-hydroxybutyryl-CoA dehydrogenase, nucleic acids encoding the same, vectors comprising the nucleic acids, and cells comprising the polypeptide variants and/or thiolase, the nucleic acids, and/or the vectors. The present disclosure also provides methods of making and using the same, including methods for culturing cells, and for the production of various products, including 3-hydroxybutyryl-CoA (3-HB-CoA), 3-hydroxybutyraldehyde (3-HBal), 3-hydroxybutyrate (3-HB), 1,3-butanediol (1,3-BDO), and esters and amides thereof, and products made from any of these.

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

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

Genetically engineered bacteria, pharmaceutical compositions thereof, and methods of modulating and treating disorders associated with hyperammonemia are disclosed.

Protein-rich nutrient supplements and animal feed supplements derived from an anaerobic bacterial process are generated through a myriad of cell rupturing and protein fractionation/purification processes. Bacterial fermentation systems and methods of obtaining one or more protein-containing portions from a fermentation process using carbon monoxide-containing gaseous substrates are provided. The invention further provides compositions of protein-rich nutrient supplements with useful applications for intake by a variety of different animals and humans.