Recombinant Lactococcus lactis for efficient conversion of cellodextrins into L‐lactic acid

Lactic acid bacteria (LAB) are among the most interesting organisms for industrial processes with a long history of application as food starters and biocontrol agents, and an underexploited potential for biorefineries converting biomass into high‐value compounds. Lactic acid (LA), their main fermentation product, is among the most requested chemicals owing to its broad range of applications. Notably, LA polymers, that is, polylactides, have high potential as biodegradable substitutes of fossil‐derived plastics. However, LA production by LAB fermentation is currently too expensive for polylactide to be cost‐competitive with traditional plastics. LAB have complex nutritional requirements and cannot ferment inexpensive substrates such as cellulose. Metabolic engineering could help reduce such nutritional requirements and enable LAB to directly ferment low‐cost polysaccharides. Here, we engineered a Lactococcus lactis strain which constitutively secretes a β‐glucosidase and an endoglucanase. The recombinant strain can grow on cellooligosaccharides up to at least cellooctaose and efficiently metabolizes them to L‐LA in single‐step fermentation. This is the first report of a LAB able to directly metabolize cellooligosaccharides longer that cellohexaose and a significant step toward cost‐sustainable consolidated bioprocessing of cellulose into optically pure LA. In this study, we have engineered a Lactococcus lactis which constitutively secretes a (β‐glucosidase and an endoglucanase). The recombinant strain can grow on cellooligosaccharides up to at least cellooctaose and efficiently metabolizes them to L‐LA in single‐step fermentation. This is the first report of a LAB able to directly metabolize cellooligosaccharides longer than cellohexaose and a significant step toward cost‐sustainable consolidated bioprocessing of cellulose into optically pure LA.