Kinetic Analysis of Growth Rate, ATP, and Pigmentation Suggests an Energy-spilling Function for the Pigment Prodigiosin of Serratia Marcescens
Overview
Authors
Affiliations
Serratia marcescens is a gram-negative environmental bacterium and opportunistic pathogen. S. marcescens expresses prodigiosin, a bright red and cell-associated pigment which has no known biological function for producing cells. We present here a kinetic model relating cell, ATP, and prodigiosin concentration changes for S. marcescens during cultivation in batch culture. Cells were grown in a variety of complex broth media at temperatures which either promoted or essentially prevented pigmentation. High growth rates were accompanied by large decreases in cellular prodigiosin concentration; low growth rates were associated with rapid pigmentation. Prodigiosin was induced most strongly during limited growth as the population transitioned to stationary phase, suggesting a negative effect of this pigment on biomass production. Mathematically, the combined rate of formation of biomass and bioenergy (as ATP) was shown to be equivalent to the rate of prodigiosin production. Studies with cyanide inhibition of both oxidative phosphorylation and pigment production indicated that rates of biomass and net ATP synthesis were actually higher in the presence of cyanide, further suggesting a negative regulatory role for prodigiosin in cell and energy production under aerobic growth conditions. Considered in the context of the literature, these results suggest that prodigiosin reduces ATP production by a process termed energy spilling. This process may protect the cell by limiting production of reactive oxygen compounds. Other possible functions for prodigiosin as a mediator of cell death at population stationary phase are discussed.
ATP biosensor reveals microbial energetic dynamics and facilitates bioproduction.
Mu X, Evans T, Zhang F Nat Commun. 2024; 15(1):5299.
PMID: 38906854 PMC: 11192931. DOI: 10.1038/s41467-024-49579-1.
McCarlie S, Steyn L, du Preez L, Boucher C, Hernandez J, Bragg R Microorganisms. 2023; 11(3).
PMID: 36985138 PMC: 10057160. DOI: 10.3390/microorganisms11030564.
Lejeune C, Sago L, Cornu D, Redeker V, Virolle M Front Microbiol. 2022; 12:813993.
PMID: 35392450 PMC: 8981147. DOI: 10.3389/fmicb.2021.813993.
Fnr Negatively Regulates Prodigiosin Synthesis in sp. ATCC 39006 During Aerobic Fermentation.
Sun D, Zhou X, Liu C, Zhu J, Ru Y, Liu W Front Microbiol. 2021; 12:734854.
PMID: 34603264 PMC: 8485047. DOI: 10.3389/fmicb.2021.734854.
Identification of Essential Genes Associated With Prodigiosin Production in FZSF02.
Jia X, Liu F, Zhao K, Lin J, Fang Y, Cai S Front Microbiol. 2021; 12:705853.
PMID: 34367107 PMC: 8339205. DOI: 10.3389/fmicb.2021.705853.