Esther Wing Kwan Mak, Kendra A. Turk-Kubo, David A. Caron, Rachel C. Harbeitner, Jonathan D. Magasin, Tyler H. Coale, Kyoko Hagino, Yoshihito Takano, Tomohiro Nishimura, Masao Adachi, Jonathan P. Zehr
{"title":"Phagotrophy in the nitrogen-fixing haptophyte Braarudosphaera bigelowii","authors":"Esther Wing Kwan Mak, Kendra A. Turk-Kubo, David A. Caron, Rachel C. Harbeitner, Jonathan D. Magasin, Tyler H. Coale, Kyoko Hagino, Yoshihito Takano, Tomohiro Nishimura, Masao Adachi, Jonathan P. Zehr","doi":"10.1111/1758-2229.13312","DOIUrl":null,"url":null,"abstract":"<p>Biological nitrogen fixation provides fixed nitrogen for microbes living in the oligotrophic open ocean. UCYN-A2, the previously known symbiont of <i>Braarudosphaera bigelowii</i>, now believed to be an early-stage <i>B. bigelowii</i> organelle that exchanges fixed nitrogen for fixed carbon, is globally distributed. Indirect evidence suggested that <i>B. bigelowii</i> might be a mixotrophic (phagotrophic) phototrophic flagellate. The goal of this study was to determine if <i>B. bigelowii</i> can graze on bacteria using several independent approaches. The results showed that <i>B. bigelowii</i> grazed on co-occurring bacteria at a rate of 5–7 cells/h/<i>B. bigelowii</i> and that the overall grazing rate was significantly higher at nighttime than at daytime. Bacterial abundance changes, assessed with 16S rRNA gene amplicon sequencing analysis, may have indicated preferential grazing by <i>B. bigelowii</i> on specific bacterial genotypes. In addition, Lysotracker™ staining of <i>B. bigelowii</i> suggested digestive activity inside <i>B. bigelowii</i>. Carbon and nitrogen fixation measurements revealed that the carbon demand of <i>B. bigelowii</i> could not be fulfilled by photosynthesis alone, implying supplementation by heterotrophy. These independent lines of evidence together revealed that <i>B. bigelowii</i> engages in phagotrophy, which, beyond serving as a supplementary source of carbon and energy, may also facilitate the indirect assimilation of inorganic nutrients.</p>","PeriodicalId":163,"journal":{"name":"Environmental Microbiology Reports","volume":"16 4","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11269211/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Microbiology Reports","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1758-2229.13312","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Biological nitrogen fixation provides fixed nitrogen for microbes living in the oligotrophic open ocean. UCYN-A2, the previously known symbiont of Braarudosphaera bigelowii, now believed to be an early-stage B. bigelowii organelle that exchanges fixed nitrogen for fixed carbon, is globally distributed. Indirect evidence suggested that B. bigelowii might be a mixotrophic (phagotrophic) phototrophic flagellate. The goal of this study was to determine if B. bigelowii can graze on bacteria using several independent approaches. The results showed that B. bigelowii grazed on co-occurring bacteria at a rate of 5–7 cells/h/B. bigelowii and that the overall grazing rate was significantly higher at nighttime than at daytime. Bacterial abundance changes, assessed with 16S rRNA gene amplicon sequencing analysis, may have indicated preferential grazing by B. bigelowii on specific bacterial genotypes. In addition, Lysotracker™ staining of B. bigelowii suggested digestive activity inside B. bigelowii. Carbon and nitrogen fixation measurements revealed that the carbon demand of B. bigelowii could not be fulfilled by photosynthesis alone, implying supplementation by heterotrophy. These independent lines of evidence together revealed that B. bigelowii engages in phagotrophy, which, beyond serving as a supplementary source of carbon and energy, may also facilitate the indirect assimilation of inorganic nutrients.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.