Construction of prophage‐free and highly‐transformable Limosilactobacillus reuteri strains and their use for production of 1,3‐propanediol

Abstract The lactic acid bacterium Limosilactobacillus reuteri (formerly Lactobacillus reuteri ) is a desirable host for the production of 1,3‐propanediol (1,3‐PDO) from glycerol when 1,3‐PDO is used in the food or cosmetic industry. However, the production is hindered by strain instability, causing cell lysis, and difficult gene manipulation. This study reveals that the stability of L. reuteri DSM 20016 and its 1,3‐PDO production, especially in the alcohol dehydrogenases (ADHs)‐deletion mutants, are greatly enhanced after the deletion of two prophages (Φ3 and Φ4) present in the L. reuteri 's chromosome. The resulting phage‐free and ADHs‐deletion mutant could produce >825 mM 1,3‐PDO in 48 h without cell lysis at the theoretical maximum yield on glucose of ~2 mol/mol. Compared to the wild‐type strain, the mutant exhibited a 45.2% increase in 1,3‐PDO production titer and a 2.1‐fold increase in yield. In addition, this study reports that the transformation efficiency of L. reuteri Δ adh2 Δ adh6 mutant strains were greatly enhanced by >300‐fold after the deletion of prophage Φ3, probably due to the removal of a restriction‐modification (RM) system which resides in the phage genome. With improved stability and higher transformation efficiency, recombinant L. reuteri DSM 20016 Δ adh 2Δ adh 6ΔΦ3ΔΦ4 can be a more reliable and amenable host for industrial applications.