SUMMARYCircadian regulation produces a biological measure of time within cells. The daily cycle in the availability of light for photosynthesis causes dramatic changes in biochemical processes in photosynthetic organisms, with the circadian clock having crucial roles in adaptation to these fluctuating conditions. Correct alignment between the circadian clock and environmental day–night cycles maximizes plant productivity through its regulation of metabolism. Therefore, the processes that integrate circadian regulation with metabolism are key to understanding how the circadian clock contributes to plant productivity. This forms an important part of exploiting knowledge of circadian regulation to enhance sustainable crop production. Here, we examine the roles of circadian regulation in metabolic processes in source and sink organ structures of Arabidopsis. We also evaluate possible roles for circadian regulation in root exudation processes that deposit carbon into the soil, and the nature of the rhythmic interactions between plants and their associated microbial communities. Finally, we examine shared and differing aspects of the circadian regulation of metabolism between Arabidopsis and other model photosynthetic organisms, and between circadian control of metabolism in photosynthetic and non‐photosynthetic organisms. This synthesis identifies a variety of future research topics, including a focus on metabolic processes that underlie biotic interactions within ecosystems.

Wild bacteria, from the open ocean to the gut, experience persistent nutrient limitation. This fundamentally affects bacterial physiology and metabolism and has profound impacts on their infection by bacterial viruses (bacteriophages). For virulent bacteriophages, which cannot enter a lysogenic state, this poses a problem for environmental persistence. Here we demonstrate that virulent bacteriophage SPP1 productively infects nutrient-limited stationary phase cultures of the Gram-positive bacteriumBacillus subtilis. Slow production and release of low numbers of infective viral particles resulted from a prolonged infection of the host population. Extensive culture lysis was greatly delayed, releasing additional viral particles and promoting fresh infections of bacterial survivors. Induced overproduction of cell surface bacteriophage receptor YueB, compensating for its scarcity in stationary phase, expedited infection dynamics under nutrient-limiting conditions, but did not change overall infection productivity. The temporal program of SPP1 gene expression differed from exponential phase, consistent with a prolonged, persistent mode of infection. Reduced expression of genes coding viral structural proteins correlated with the low yield of infectious particles. Importantly, exogenous influx of the carbon source maltose enhanced viral particle production. Our results uncover a novel adaptive strategy of a lytic phage for productive infection of nutrient-limited bacterial populations through persistent, exhaustive infection.

During peptidoglycan recycling (PR) bacteria can recover extracellular fragments of peptidoglycan (PGN) liberated by peptidoglycan turnover (PT) during cell growth and division, and reuse them in cell wall biosynthesis or central carbon metabolism. In Gram-negative bacteria, PR has been well studied, and functions in the induction of resistance to certain classes of antibiotics, and in host-pathogen interaction. However, while Gram-negative cell envelope architecture allows for highly efficient PR, Gram-positive bacteria, which lack an outer cell membrane and are instead enclosed by a glycopolymer layer, can shed large quantities of PGN-derived material to the external environment during growth. Nonetheless, the occurrence of PR was recently demonstrated in several Gram-positive bacteria, including the Gram-positive bacterial pathogen Staphylococcus aureus, and its potential adaptive functions are largely unexplored. Given the known roles of PR in Gram-negative bacteria, and that Gram-positive bacteria include several important human pathogens, we asked what role PR may play during Gram-positive pathogen-host interaction. Using the model insect host Drosophila melanogaster, we demonstrate that S. aureus mutants impaired in extracellular PGN hydrolysis (Δatl) and PGN fragment uptake (ΔmurP) show differential virulence compared to their wild-type counterpart. This was linked to increased activation of the D. melanogaster Toll-cascade by spent supernatant from the Δatl mutant. Thus, we propose that S. aureus, and potentially other Gram-positive bacteria, may use extracellular PGN degradation during PT to simultaneously process PGN fragments for recycling and for immune evasion, while recovery and metabolism of peptidoglycan fragments during PR may play more subtle roles in determining virulence.