Another Breaker of the Wall: the Biological Function of the Usp45 Protein of Lactococcus lactis

• Published in: Applied and environmental microbiology 2020-08, Vol.86 (16), p.1
• Main Authors: Hernandez-Valdes, Jhonatan A, Huang, Chenxi, Kok, Jan, Kuipers, Oscar P
• Format: Article
• Language: English
• Subjects: Bacteria; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Cell division; Cell Division - physiology; Cell Wall - metabolism; Cell walls; Deactivation; Food Microbiology; Functional foods & nutraceuticals; Galactose; Gene Expression Regulation, Bacterial; Gram-positive bacteria; Homology; Hydrolase; Inactivation; Lactococcus lactis; Lactococcus lactis - genetics; Lactococcus lactis - metabolism; Peptidoglycan hydrolase; Phenotypes; Promoter Regions, Genetic; Proteins; Spotlight
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.00903-20

is a Gram-positive bacterium that is widely used as a cell factory for the expression of heterologous proteins that are relevant in the pharmaceutical and nutraceutical fields. The signal peptide of the major secreted protein of , Usp45, has been employed extensively in engineering strategies to secrete proteins of interest. However, the biological function of Usp45 has remained obscure despite more than 25 years of research. Studies on Usp45 homologs in other Gram-positive bacteria suggest that Usp45 may play a role in cell wall turnover processes. Here, we show the effect of inactivation and overexpression of the gene on growth, phenotype, and cell division. Our results are in agreement with those obtained in streptococci and demonstrate that the Usp45 protein is essential for proper cell division. We also show that the promoter is highly activated by galactose. Overall, our results indicate that Usp45 mediates cell separation, probably by acting as a peptidoglycan hydrolase. The cell wall, composed mainly of peptidoglycan, is key to maintaining the cell shape and protecting the cell from bursting. Peptidoglycan degradation by peptidoglycan hydrolysis and autolysins occurs during growth and cell division. Since peptidoglycan hydrolases are important for virulence, envelope integrity, and regulation of cell division, it is valuable to investigate their function and regulation. Notably, PcsB-like proteins such as Usp45 have been proposed as new targets for antimicrobial drugs and could also be target for the development of food-grade suicide systems. In addition, although various other expression and secretion systems have been developed for use in , the most-used signal peptide for protein secretion in this bacterium is that of the Usp45 protein. Thus, elucidating the biological function of Usp45 and determining the factors affecting its expression would contribute to optimize several applications.