Isaac S White, Daniel P Canniffe, Andrew Hitchcock
{"title":"The diversity of physiology and metabolism in chlorophototrophic bacteria.","authors":"Isaac S White, Daniel P Canniffe, Andrew Hitchcock","doi":"10.1016/bs.ampbs.2025.02.003","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2025.02.003","url":null,"abstract":"<p><p>Photosynthesis by (bacterio)chlorophyll-producing organisms (\"chlorophototrophy\") sustains virtually all life on Earth, providing the biosphere with food and energy. The oxygenic process carried out by plants, algae and cyanobacteria also generates the oxygen we breathe, and ancient cyanobacteria were responsible for oxygenating the atmosphere, creating the conditions that allowed the evolution of complex life. Cyanobacteria were also the endosymbiotic progenitors of chloroplasts, play major roles in biogeochemical cycles and as primary producers in aquatic ecosystems, and act as genetically tractable model organisms for studying oxygenic photosynthesis. In addition to the Cyanobacteriota, eight other bacterial phyla, namely Proteobacteria/Pseudomonadota, Chlorobiota, Chloroflexota, Bacillota, Acidobacteriota, Gemmatimonadota, Vulcanimicrobiota and Myxococcota contain at least one putative chlorophototrophic species, all of which perform a variant of anoxygenic photosynthesis, which does not yield oxygen as a by-product. These chlorophototrophic organisms display incredible diversity in the habitats that they colonise, and in their biochemistry, physiology and metabolism, with variation in the light-harvesting complexes and pigments they produce to utilise solar energy. Whilst some are very well understood, such as the proteobacterial 'purple bacteria', others have only been identified in the last few years and therefore relatively little is known about them - especially those that have not yet been isolated and cultured. In this chapter, we aim to summarise and compare the photosynthetic physiology and central metabolic processes of chlorophototrophic members from the nine phyla in which they are found, giving both a short historical perspective and highlighting gaps in our understanding.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"1-98"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Vitaliy B Borisov, Giorgio Giardina, Gianluca Pistoia, Elena Forte
{"title":"Cytochrome bd-type oxidases and environmental stressors in microbial physiology.","authors":"Vitaliy B Borisov, Giorgio Giardina, Gianluca Pistoia, Elena Forte","doi":"10.1016/bs.ampbs.2024.05.001","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2024.05.001","url":null,"abstract":"<p><p>Cytochrome bd is a tri-haem copper-free terminal oxidase of many respiratory chains of prokaryotes with unique structural and functional characteristics. As the other membrane-bound terminal oxidases, this enzyme couples the four-electron reduction of oxygen to water with the generation of a proton motive force used for ATP synthesis but the molecular mechanism does not include proton pumping. Beyond its bioenergetic role, cytochrome bd is involved in resistance to several stressors and affords protection against oxidative and nitrosative stress. These features agree with its expression in many bacterial pathogens. The importance for bacterial virulence and the absence of eukaryotic homologues make this enzyme an ideal target for new antimicrobial drugs. This review aims to provide an update on the current knowledge about cytochrome bd in light of recent advances in the structural characterisation of this enzyme, focussing on its reactivity with environmental stressors.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"199-255"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Organohalide respiration in Dehalococcoides strains represents a novel mode of proton motive force generation.","authors":"Lorenz Adrian, R Gary Sawers, Darja Deobald","doi":"10.1016/bs.ampbs.2024.12.001","DOIUrl":"10.1016/bs.ampbs.2024.12.001","url":null,"abstract":"<p><p>Dehalococcoides strains grow obligately by respiration with hydrogen as an electron donor and halogenated compounds as terminal electron acceptors, catalysed by a single membrane-integrated protein supercomplex. Many insights have been gained into the respiratory complex based on physiological experiments, biochemical analyses, genome sequencing, and proteomics. Recent data acquired from activity tests with deuterated water and whole cells revealed the mode of energy conservation by this respiratory complex. The data shows that the proton required for periplasmic dehalogenation originates from inside the cell, suggesting an electrogenic protonation of the electron acceptor, while two protons are released into the periplasm by hydrogen oxidation. This surprisingly simple mechanism of pmf generation aligns with the subunit composition of the respiratory complex, the orientation of the subunits in the membrane, the absence of quinones as electron mediators, the rigidity of the cell membrane, as evidenced by its phospholipid fatty acid composition, and with proton channels formed by protonatable amino acid residues identified in the AlphaFold2-predicted structure of one of the membrane-spanning subunits. The respiration model is characterised by: (i) electrogenic protonation of the electron acceptor; (ii) reliance on a single protein complex for pmf generation without quinones; (iii) lack of transmembrane cytochromes; (iv) presence of both redox-active centres on the same side of the membrane, both facing the periplasm; and (v) restriction of the electron flow to periplasmic subunits of the respiratory complex. This type of respiration may represent an ancestral, quinone-free mechanism, offering inspiring new biotechnological applications.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"141-173"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Helen A Jenkins, Alun L Lloyd, Jackelyn M Kembro, David Lloyd
{"title":"Time and function in the living world.","authors":"Helen A Jenkins, Alun L Lloyd, Jackelyn M Kembro, David Lloyd","doi":"10.1016/bs.ampbs.2025.02.001","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2025.02.001","url":null,"abstract":"<p><p>We begin by discussing some historical ideas about the natural dynamics of living organisms and their complex states, from the very transient to the very persistent. We classify ultradian rhythms as being more important than most oscillatory behaviour in their distinctive properties. Then we summarise rhythmicity in three yeasts and five representative protist species. Recent discoveries about the single-celled photosynthetic alga Chlamydomonas reinhardii are then discussed as revealed by computer-controlled semi-continuous monitoring: automatic periodic measurement of the rate of phototaxis and chlorophyll a content over extended times for up to 12 days. Methodological approaches for analysing time series are discussed, including the recently developed 'GaMoSEC' procedure, providing published references to the detection and understanding of the complex behaviour of natural systems. Finally, we conclude by summarising the general significance of ultradian rhythms to the vital aspects of the biological timekeeping of coherent functionality of living systems from single-cell organisms to humans from their healthy to declining states.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"331-375"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129715","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Copper homeostasis in Streptococcus and Neisseria: Known knowns and unknown knowns.","authors":"Archie Howell, Safa Chogule, Karrera Y Djoko","doi":"10.1016/bs.ampbs.2024.11.001","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2024.11.001","url":null,"abstract":"<p><p>Our research group studies copper (Cu) homeostasis in Streptococcus and Neisseria, with a current focus on species that colonise the human oral cavity. Our early ventures into this field very quickly revealed major differences between well-characterised Cu homeostasis systems in species with well-known pathogenic potential and the uncharacterised systems in species that are considered as components of the normal healthy human microflora. In this article, we summarise the known and predicted mechanisms of Cu homeostasis in Streptococcus and Neisseria. We focus exclusively on proteins that directly sense and change (increase or decrease) cellular Cu availability. Where relevant, we make comparisons with examples from species isolated from outside the human oral cavity and from animal hosts. The emerging picture depicts diverse cellular strategies for handling Cu, even among closely related bacterial species.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"99-140"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mechna Chowdhury, Phillip J Stansfeld, Frank Sargent
{"title":"A lysis less ordinary: The bacterial Type 10 Secretion System.","authors":"Mechna Chowdhury, Phillip J Stansfeld, Frank Sargent","doi":"10.1016/bs.ampbs.2025.02.002","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2025.02.002","url":null,"abstract":"<p><p>Bacteria have evolved several different biochemical pathways to either export proteins of all shapes and sizes out of the cell cytoplasm, or to secrete those proteins into the extracellular environment. Many bacterial protein secretion systems have evolutionary links to systems used by bacteriophage to move macromolecules across membranes. The Type 10 Secretion System (T10SS) was identified in gram-negative bacteria and comprises genes that bear striking sequence similarities to those found within phage lysis cassettes. The minimum components of a T10SS are an integral membrane holin-like protein together with a peptidoglycan hydrolase. Here, we review recent research in Serratia spp., Salmonella spp, Yersinia spp, and gram-positive Clostridioides spp., and consider the evidence for different T10SS mechanisms ranging from a controlled release of proteins into the environment, to stochastic altruistic lysis of specialised populations of cells.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"175-198"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Artur Sergunin, Jakub Vávra, Dominik Pašek, Toru Shimizu, Markéta Martínková
{"title":"Multiple roles for iron in microbial physiology: Bacterial oxygen sensing by heme-based sensors.","authors":"Artur Sergunin, Jakub Vávra, Dominik Pašek, Toru Shimizu, Markéta Martínková","doi":"10.1016/bs.ampbs.2024.10.001","DOIUrl":"https://doi.org/10.1016/bs.ampbs.2024.10.001","url":null,"abstract":"<p><p>Bacterial oxygen sensing embodies a fascinating interplay between evolutionary pressures and physiological adaptations to varying oxygen levels. Throughout Earth's history, the composition of the atmosphere has undergone significant changes, from anoxic conditions to the gradual accumulation of oxygen. In response, microbial life has evolved diverse strategies to cope with these shifting oxygen levels, ranging from anaerobic metabolism to oxygen-dependent pathways crucial for energy production and cellular processes typical for eukaryotic, multicellular organisms. Of particular interest is the role of iron in bacterial oxygen sensing systems, which play pivotal roles in adaptation to changing oxygen levels. Only free iron, heme-iron, and non-heme iron directly sense oxygen. These iron-containing proteins, such as heme-containing sensors and iron-sulfur cluster proteins, regulate the expression of genes and activity of enzymes involved in oxidative stress defence, virulence, and biofilm formation, highlighting their significance in bacterial pathogenesis and environmental adaptation. Special attention in the review is paid to the mechanisms of oxygen detection and signal transduction from heme-containing sensing to functional domains in the case of bacterial heme-based oxygen sensors.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"86 ","pages":"257-329"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129744","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andreia I Pimenta, Raquel M Bernardino, Inês A C Pereira
{"title":"Role of sulfidogenic members of the gut microbiota in human disease.","authors":"Andreia I Pimenta, Raquel M Bernardino, Inês A C Pereira","doi":"10.1016/bs.ampbs.2024.04.003","DOIUrl":"10.1016/bs.ampbs.2024.04.003","url":null,"abstract":"<p><p>The human gut flora comprises a dynamic network of bacterial species that coexist in a finely tuned equilibrium. The interaction with intestinal bacteria profoundly influences the host's development, metabolism, immunity, and overall health. Furthermore, dysbiosis, a disruption of the gut microbiota, can induce a variety of diseases, not exclusively associated with the intestinal tract. The increased consumption of animal protein, high-fat and high-sugar diets in Western countries has been implicated in the rise of chronic and inflammatory illnesses associated with dysbiosis. In particular, this diet leads to the overgrowth of sulfide-producing bacteria, known as sulfidogenic bacteria, which has been linked to inflammatory bowel diseases and colorectal cancer, among other disorders. Sulfidogenic bacteria include sulfate-reducing bacteria (Desulfovibrio spp.) and Bilophila wadsworthia among others, which convert organic and inorganic sulfur compounds to sulfide through the dissimilatory sulfite reduction pathway. At high concentrations, sulfide is cytotoxic and disrupts the integrity of the intestinal epithelium and mucus barrier, triggering inflammation. Besides producing sulfide, B. wadsworthia has revealed significant pathogenic potential, demonstrated in the ability to cause infection, adhere to intestinal cells, promote inflammation, and compromise the integrity of the colonic mucus layer. This review delves into the mechanisms by which taurine and sulfide-driven gut dysbiosis contribute to the pathogenesis of sulfidogenic bacteria, and discusses the role of these gut microbes, particularly B. wadsworthia, in human diseases.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"85 ","pages":"145-200"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The globins of cyanobacteria and green algae: An update.","authors":"Juliette T J Lecomte, Eric A Johnson","doi":"10.1016/bs.ampbs.2024.04.004","DOIUrl":"10.1016/bs.ampbs.2024.04.004","url":null,"abstract":"<p><p>The globin superfamily of proteins is ancient and diverse. Regular assessments based on the increasing number of available genome sequences have elaborated on a complex evolutionary history. In this review, we present a summary of a decade of advances in characterising the globins of cyanobacteria and green algae. The focus is on haem-containing globins with an emphasis on recent experimental developments, which reinforce links to nitrogen metabolism and nitrosative stress response in addition to dioxygen management. Mention is made of globins that do not bind haem to provide an encompassing view of the superfamily and perspective on the field. It is reiterated that an effort toward phenotypical and in-vivo characterisation is needed to elucidate the many roles that these versatile proteins fulfil in oxygenic photosynthetic microbes. It is also proposed that globins from oxygenic organisms are promising proteins for applications in the biotechnology arena.</p>","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"85 ","pages":"97-144"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Preface.","authors":"Robert K Poole, David J Kelly","doi":"10.1016/S0065-2911(24)00029-8","DOIUrl":"10.1016/S0065-2911(24)00029-8","url":null,"abstract":"","PeriodicalId":519928,"journal":{"name":"Advances in microbial physiology","volume":"85 ","pages":"xi"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768426","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}