Molecular mechanisms underlying iron and phosphorus co-limitation responses in the nitrogen-fixing cyanobacterium Crocosphaera | The ISME Journal

2022-09-03 08:33:45 By : Ms. Linda Lee

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In the nitrogen-limited subtropical gyres, diazotrophic cyanobacteria, including Crocosphaera, provide an essential ecosystem service by converting dinitrogen (N2) gas into ammonia to support primary production in these oligotrophic regimes. Natural gradients of phosphorus (P) and iron (Fe) availability in the low-latitude oceans constrain the biogeography and activity of diazotrophs with important implications for marine biogeochemical cycling. Much remains unknown regarding Crocosphaera’s physiological and molecular responses to multiple nutrient limitations. We cultured C. watsonii under Fe, P, and Fe/P (co)-limiting scenarios to link cellular physiology with diel gene expression and observed unique physiological and transcriptional profiles for each treatment. Counterintuitively, reduced growth and N2 fixation resource use efficiencies (RUEs) for Fe or P under P limitation were alleviated under Fe/P co-limitation. Differential gene expression analyses show that Fe/P co-limited cells employ the same responses as single-nutrient limited cells that reduce cellular nutrient requirements and increase responsiveness to environmental change including smaller cell size, protein turnover (Fe-limited), and upregulation of environmental sense-and-respond systems (P-limited). Combined, these mechanisms enhance growth and RUEs in Fe/P co-limited cells. These findings are important to our understanding of nutrient controls on N2 fixation and the implications for primary productivity and microbial dynamics in a changing ocean.

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The physiological data collected from this study are available from BCO-DMO online (http://bcodmo.org). Raw RNAseq reads for differential gene expression analyses are deposited at NCBI’s SRA under BioProject PRJNA807802. All scripts to recreate the differential gene expression analyses, statistical analyses, and visualizations are available at https://github.com/yang-nina/CrocosphaeraFePColimitation.

Moore CM, Mills MM, Arrigo KR, Berman-Frank I, Bopp L, Boyd PW, et al. Processes and patterns of oceanic nutrient limitation. Nat Geosci. 2013; https://doi.org/10.1038/ngeo1765.

Redfield AC. The biological control of chemical factors in the environment. Am Sci. 1958;46:205–21.

Sohm JA, Webb EA, Capone DG. Emerging patterns of marine nitrogen fixation. Nat Rev Microbiol. 2011;9:499–508.

CAS  PubMed  Article  Google Scholar 

Zehr JP, Capone DG. Changing perspectives in marine nitrogen fixation. Science 2020;368:eaay9514.

CAS  PubMed  Article  Google Scholar 

Karl D, Letelier R, Tupas L, Dore J, Christian J, Hebel D. The role of nitrogen fixation in biogeochemical cycling in the subtropical North Pacific Ocean. Nature 1997;388:533–8.

Tang W, Cerdán-García E, Berthelot H, Polyviou D, Wang S, Baylay A, et al. New insights into the distributions of nitrogen fixation and diazotrophs revealed by high-resolution sensing and sampling methods. ISME J. 2020;14:2514–26.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Tang W, Wang S, Fonseca-Batista D, Dehairs F, Gifford S, Gonzalez AG, et al. Revisiting the distribution of oceanic N2 fixation and estimating diazotrophic contribution to marine production. Nat Commun. 2019; https://doi.org/10.1038/s41467-019-08640-0.

Capone DG, Burns JA, Montoya JP, Subramaniam A, Mahaffey C, Gunderson T, et al. Nitrogen fixation by Trichodesmium spp.: an important source of new nitrogen to the tropical and subtropical North Atlantic Ocean. Global Biogeochem Cycles. 2005; https://doi.org/10.1029/2004GB002331.

Qu P-P, Fu F-X, Kling JD, Huh M, Wang X, Hutchins DA. Distinct responses of the nitrogen-fixing marine cyanobacterium Trichodesmium to a thermally variable environment as a function of phosphorus availability. Front Microbiol. 2019; https://doi.org/10.3389/fmicb.2019.01282.

Orchard ED, Webb EA, Dyhrman ST. Molecular analysis of the phosphorus starvation response in Trichodesmium spp. Environ Microbiol. 2009;11:2400–11.

CAS  PubMed  Article  Google Scholar 

Capone DG, Zehr JP, Paerl HW, Bergman B, Carpenter EJ. Trichodesmium, a globally significant marine cyanobacterium. Science. 1997;276:1221–9.

Capone DG, Carpenter EJ. Nitrogen fixation in the marine environment. Science. 1982;217:1140–2.

CAS  PubMed  Article  Google Scholar 

Zehr JP, Waterbury JB, Turner PJ, Montoya JP, Omoregie E, Steward GF, et al. Unicellular cyanobacteria fix N2 in the subtropical North Pacific Ocean. Nature. 2001;412:635–8.

CAS  PubMed  Article  Google Scholar 

Shi T, Ilikchyan I, Rabouille S, Zehr JP. Genome-wide analysis of diel gene expression in the unicellular N2-fixing cyanobacterium Crocosphaera watsonii WH 8501. ISME J. 2010;4:621–32.

CAS  PubMed  Article  Google Scholar 

Bench SR, Heller P, Frank I, Arciniega M, Shilova IN, Zehr JP. Whole genome comparison of six Crocosphaera watsonii strains with differing phenotypes. J Phycol. 2013;49:786–801.

PubMed  PubMed Central  Article  Google Scholar 

Dugenne M, Henderikx Freitas F, Wilson ST, Karl DM, White AE. Life and death of Crocosphaera sp. in the Pacific Ocean: Fine scale predator–prey dynamics. Limnol Oceanogr. 2020;65:2603–17.

Moisander PH, Beinart RA, Hewson I, White AE, Johnson KS, Carlson CA, et al. Unicellular cyanobacterial distributions broaden the oceanic N2 fixation domain. Science. 2010;327:1512–4.

CAS  PubMed  Article  Google Scholar 

Detoni AMS, Subramaniam A, Haley ST, Dyhrman ST, Calil PHR. Cyanobacterial diazotroph distributions in the Western South Atlantic. Front Mar Sci. 2022; https://doi.org/10.3389/fmars.2022.856643.

Webb EA, Moffett JW, Waterbury JB. Iron stress in open-ocean cyanobacteria (Synechococcus, Trichodesmium, and Crocosphaera spp.): identification of the IdiA protein. Appl Environ Microbiol. 2001; https://doi.org/10.1128/AEM.67.12.5444-5452.2001.

Jacq V, Ridame C, L’Helguen S, Kaczmar F, Saliot A. Response of the unicellular diazotrophic cyanobacterium Crocosphaera watsonii to iron limitation. PLoS One. 2014;9:e86749.

PubMed  PubMed Central  Article  CAS  Google Scholar 

Garcia NS, Fu F, Sedwick PN, Hutchins DA. Iron deficiency increases growth and nitrogen-fixation rates of phosphorus-deficient marine cyanobacteria. ISME J. 2015;9:238–45.

CAS  PubMed  Article  Google Scholar 

Lin S, Litaker RW, Sunda WG. Phosphorus physiological ecology and molecular mechanisms in marine phytoplankton. J Phycol. 2016;52:10–36.

CAS  PubMed  Article  Google Scholar 

Held NA, McIlvin MR, Moran DM, Laub MT, Saito MA. Unique patterns and biogeochemical relevance of two-component sensing in marine bacteria. mSystems. 2019; https://doi.org/10.1128/mSystems.00317-18.

Capra EJ, Laub MT. Evolution of two-component signal transduction systems. Annu Rev Microbiol. 2012;66:325–47.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Shi T, Sun Y, Falkowski PG. Effects of iron limitation on the expression of metabolic genes in the marine cyanobacterium Trichodesmium erythraeum IMS101. Environ Microbiol. 2007;9:2945–56.

CAS  PubMed  Article  Google Scholar 

Schoffman H, Lis H, Shaked Y, Keren N. Iron–nutrient interactions within phytoplankton. Front Plant Sci. 2016; https://doi.org/10.3389/fpls.2016.01223.

Hutchins DA, Sañudo-Wilhelmy SA. The enzymology of ocean global change. Ann Rev Mar Sci. 2022;14:187–211.

Capone DG. An iron curtain in the Atlantic Ocean forms a biogeochemical divide. Proc Natl Acad Sci USA 2014;111:1231–2.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Rouco M, Frischkorn KR, Haley ST, Alexander H, Dyhrman ST. Transcriptional patterns identify resource controls on the diazotroph Trichodesmium in the Atlantic and Pacific oceans. ISME J. 2018;12:1486–95.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Dyhrman ST, Haley ST. Phosphorus scavenging in the unicellular marine diazotroph Crocosphaera watsonii. Appl Environ Microbiol. 2006;72:1452–8.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Pereira N, Shilova IN, Zehr JP. Use of the high‐affinity phosphate transporter gene, pstS, as an indicator for phosphorus stress in the marine diazotroph Crocosphaera watsonii (Chroococcales, Cyanobacteria). J Phycol. 2019;55:752–61.

CAS  PubMed  Article  Google Scholar 

Pereira N, Shilova IN, Zehr JP. Molecular markers define progressing stages of phosphorus limitation in the nitrogen-fixing cyanobacterium, Crocosphaera. J Phycol. 2016;52:274–82.

CAS  PubMed  Article  Google Scholar 

Frischkorn KR, Haley ST, Dyhrman ST. Transcriptional and proteomic choreography under phosphorus deficiency and re-supply in the N2 fixing cyanobacterium Trichodesmium erythraeum. Front Microbiol. 2019; https://doi.org/10.3389/fmicb.2019.00330.

Bibby TS, Nield J, Barber J. Iron deficiency induces the formation of an antenna ring around trimeric photosystem I in cyanobacteria. Nature 2001;412:743–5.

CAS  PubMed  Article  Google Scholar 

Chen HYS, Bandyopadhyay A, Pakrasi HB. Function, regulation and distribution of IsiA, a membrane-bound chlorophyll a-antenna protein in cyanobacteria. Photosynthetica. 2018;56:322–33.

Hewson I, Poretsky RS, Beinart RA, White AE, Shi T, Bench SR, et al. In situ transcriptomic analysis of the globally important keystone N2-fixing taxon Crocosphaera watsonii. ISME J. 2009;3:618–31.

CAS  PubMed  Article  Google Scholar 

LaRoche J, Boyd PW, McKay RML, Geider RJ. Flavodoxin as an in situ marker for iron stress in phytoplankton. Nature. 1996;382:802–5.

Chappell PD, Webb EA. A molecular assessment of the iron stress response in the two phylogenetic clades of Trichodesmium. Environ Microbiol. 2010;12:13–27.

CAS  PubMed  Article  Google Scholar 

Held NA, Waterbury JB, Webb EA, Kellogg RM, McIlvin MR, Jakuba M, et al. Dynamic diel proteome and daytime nitrogenase activity supports buoyancy in the cyanobacterium Trichodesmium. Nat Microbiol. 2022;7:300–11.

CAS  PubMed  Article  Google Scholar 

Saito MA, Bertrand EM, Dutkiewicz S, Bulygin VV, Moran DM, Monteiro FM, et al. Iron conservation by reduction of metalloenzyme inventories in the marine diazotroph Crocosphaera watsonii. Proc Natl Acad Sci USA 2011;108:2184–9.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Mills MM, Ridame C, Davey M, LaRoche J, Geider RJ. Iron and phosphorus co-limit nitrogen fixation in the eastern tropical North Atlantic. Nature. 2004;429:292–4.

CAS  PubMed  Article  Google Scholar 

Held NA, Webb EA, McIlvin MM, Hutchins DA, Cohen NR, Moran DM, et al. Co-occurrence of Fe and P stress in natural populations of the marine diazotroph Trichodesmium. Biogeosciences. 2020;17:2537–51.

Cérdan-García E, Baylay A, Polyviou D, Woodward EMS, Wrightson L, Mahaffey C, et al. Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability. ISME J. 2021; https://doi.org/10.1038/s41396-021-01151-1.

Walworth NG, Fu F-X, Webb EA, Saito MA, Moran D, Mcllvin MR, et al. Mechanisms of increased Trichodesmium fitness under iron and phosphorus co-limitation in the present and future ocean. Nat Commun. 2016; https://doi.org/10.1038/ncomms12081.

Price NM, Harrison GI, Hering JG, Hudson RJ, Nirel PMV, Palenik B, et al. Preparation and chemistry of the artificial algal culture medium Aquil. Biol Oceanogr. 1989;6:443–61.

Yang N, Merkel CA, Lin Y-A, Levine NM, Hawco NJ, Jiang H-B, et al. Warming iron-limited oceans enhance nitrogen fixation and drive biogeographic specialization of the globally important cyanobacterium Crocosphaera. Front Mar Sci. 2021; https://doi.org/10.3389/fmars.2021.628363.

Garcia NS, Fu F-X, Breene CL, Yu EK, Bernhardt PW, Mulholland MR, et al. Combined effects of CO2 and light on large and small isolates of the unicellular N2-fixing cyanobacterium Crocosphaera watsonii from the western tropical Atlantic Ocean. Eur J Phycol. 2013;48:128–39.

Jiang H-B, Fu F-X, Rivero-Calle S, Levine NM, Sañudo-Wilhelmy SA, Qu P-P, et al. Ocean warming alleviates iron limitation of marine nitrogen fixation. Nat Clim Chang. 2018;8:709–12.

Kustka AB, Sañudo‐Wilhelmy SA, Carpenter EJ, Capone D, Burns J, Sunda WG. Iron requirements for dinitrogen‐ and ammonium‐supported growth in cultures of Trichodesmium (IMS 101): comparison with nitrogen fixation rates and iron: carbon ratios of field populations. Limnol Oceanogr. 2003;48:1869–84.

Hawco NJ, Fu F, Yang N, Hutchins DA, John SG. Independent iron and light limitation in a low-light-adapted Prochlorococcus from the deep chlorophyll maximum. ISME J. 2020;15:359–62.

PubMed  PubMed Central  Article  CAS  Google Scholar 

Andrews S. FastQC: a quality control tool for high throughput sequence data. 2010.

Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30:2114–20.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Qu P-P, Fu F-X, Wang X-W, Kling JD, Elghazzawy M, Huh M, et al. Two co-dominant nitrogen-fixing cyanobacteria demonstrate distinct acclimation and adaptation responses to cope with ocean warming. Environ Microbiol Rep. 2022; https://doi.org/10.1111/1758-2229.13041.

Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012;9:357–9.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The Sequence alignment/map format and SAMtools. Bioinformatics. 2009;25:2078–9.

PubMed  PubMed Central  Article  CAS  Google Scholar 

Liao Y, Smyth GK, Shi W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics. 2014;30:923–30.

CAS  PubMed  Article  Google Scholar 

Kanehisa M, Goto S. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000;28:27–30.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Leonhardt K, Straus NA. An iron stress operon involved in photosynthetic electron transport in the marine cyanobacterium Synechococcus sp. PCC 7002. J Gen Microbiol. 1992;138:1613–21.

CAS  PubMed  Article  Google Scholar 

Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; https://doi.org/10.1186/s13059-014-0550-8.

Yu G, Wang L-G, Han Y, He Q-Y. clusterProfiler: an R package for comparing biological themes among gene clusters. OMICS. 2012;16:284–7.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Buchfink B, Reuter K, Drost H-G. Sensitive protein alignments at tree-of-life scale using DIAMOND. Nat Methods. 2021;18:366–8.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Conesa A, Götz S, García-Gómez JM, Terol J, Talón M, Robles M. Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics. 2005;21:3674–6.

CAS  PubMed  Article  Google Scholar 

Chille E, Strand E, Neder M, Schmidt V, Sherman M, Mass T, et al. Developmental series of gene expression clarifies maternal mRNA provisioning and maternal-to-zygotic transition in a reef-building coral. BMC Genom. 2021; https://doi.org/10.1186/s12864-021-08114-y.

Jones P, Binns D, Chang H-Y, Fraser M, Li W, McAnulla C, et al. InterProScan 5: genome-scale protein function classification. Bioinformatics. 2014;30:1236–40.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Oksanen J, Guillaume Blanchet F, Friendly M, Kindt R, Legendre P, McGlinn D, et al. vegan: Community Ecology Package. R package version 2.5-7. 2020.

Finkel ZV, Beardall J, Flynn KJ, Quigg A, Rees TAV, Raven JA. Phytoplankton in a changing world: cell size and elemental stoichiometry. J Plankton Res. 2010;32:119–37.

Deng L, Cheung S, Kang C-K, Liu K, Xia X, Liu H. Elevated temperature relieves phosphorus limitation of marine unicellular diazotrophic cyanobacteria. Limnol Oceanogr. 2021; https://doi.org/10.1002/lno.11980.

Saito MA, McIlvin MR, Moran DM, Goepfert TJ, DiTullio GR, Post AF, et al. Multiple nutrient stresses at intersecting Pacific Ocean biomes detected by protein biomarkers. Science. 2014;345:1173–7.

CAS  PubMed  Article  Google Scholar 

Walworth NG, Saito MA, Lee MD, McIlvin MR, Moran DM, Kellogg RM, et al. Why environmental biomarkers work: Transcriptome-proteome correlations and modeling of multistressor experiments in the marine bacterium Trichodesmium. J Proteome Res. 2021; https://doi.org/10.1021/acs.jproteome.1c00517.

Hook SE, Gallagher EP, Batley GE. The role of biomarkers in the assessment of aquatic ecosystem health. Integr Environ Assess Manag. 2014;10:327–41.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Dron A, Rabouille S, Claquin P, Le Roy B, Talec A, Sciandra A. Light-dark (12:12) cycle of carbon and nitrogen metabolism in Crocosphaera watsonii WH8501: relation to the cell cycle. Environ Microbiol. 2012;14:967–81.

CAS  PubMed  Article  Google Scholar 

Mohr W, Intermaggio MP, LaRoche J. Diel rhythm of nitrogen and carbon metabolism in the unicellular, diazotrophic cyanobacterium Crocosphaera watsonii WH8501. Environ Microbiol. 2010;12:412–21.

CAS  PubMed  Article  Google Scholar 

Wilson ST, Aylward FO, Ribalet F, Barone B, Casey JR, Connell PE, et al. Coordinated regulation of growth, activity and transcription in natural populations of the unicellular nitrogen-fixing cyanobacterium Crocosphaera. Nat Microbiol. 2017;2:9.

Silhavy TJ, Kahne D, Walker S. The bacterial cell envelope. Cold Spring Harb Perspect Biol. 2010; https://doi.org/10.1101/cshperspect.a000414.

Scheffers D-J, Pinho MG. Bacterial cell wall synthesis: new insights from localization studies. Microbiol Mol Biol Rev. 2005;69:585–607.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Cava F, de Pedro MA. Peptidoglycan plasticity in bacteria: emerging variability of the murein sacculus and their associated biological functions. Curr Opin Microbiol. 2014;18:46–53.

CAS  PubMed  Article  Google Scholar 

Mueller EA, Levin PA. Bacterial cell wall quality control during environmental stress. mBio. 2020; https://doi.org/10.1128/mBio.02456-20.

Langklotz S, Baumann U, Narberhaus F. Structure and function of the bacterial AAA protease FtsH. Biochim Biophys Acta. 2012;1823:40–48.

CAS  PubMed  Article  Google Scholar 

Bonisteel EM, Turner BE, Murphy CD, Melanson J-R, Duff NM, Beardsall BD, et al. Strain specific differences in rates of Photosystem II repair in picocyanobacteria correlate to differences in FtsH protein levels and isoform expression patterns. PLoS One. 2018;13:e0209115.

PubMed  PubMed Central  Article  Google Scholar 

Latifi A, Ruiz M, Zhang C-C. Oxidative stress in cyanobacteria. FEMS Microbiol Rev. 2009;33:258–78.

CAS  PubMed  Article  Google Scholar 

Zehr JP, Montoya JP, Jenkins BD, Hewson I, Mondragon E, Short CM, et al. Experiments linking nitrogenase gene expression to nitrogen fixation in the North Pacific subtropical gyre. Limnol Oceanogr. 2007;52:169–83.

Benavides M, Duhamel S, Van Wambeke F, Shoemaker KM, Moisander PH, Salamon E, et al. Dissolved organic matter stimulates N2 fixation and nifH gene expression in Trichodesmium. FEMS Microbiol Lett. 2020; https://doi.org/10.1093/femsle/fnaa034.

Turk-Kubo KA, Achilles KM, Serros TRC, Ochiai M, Montoya JP, Zehr JP. Nitrogenase (nifH) gene expression in diazotrophic cyanobacteria in the Tropical North Atlantic in response to nutrient amendments. Front Microbiol. 2012; https://doi.org/10.3389/fmicb.2012.00386.

Turk KA, Rees AP, Zehr JP, Pereira N, Swift P, Shelley R, et al. Nitrogen fixation and nitrogenase (nifH) expression in tropical waters of the eastern North Atlantic. ISME J. 2011;5:1201–12.

CAS  PubMed  Article  Google Scholar 

Zehr JP, Wyman M, Miller V, Duguay L, Capone DG. Modification of the Fe protein of nitrogenase in natural populations of Trichodesmium thiebautii. Appl Environ Microbiol. 1993;59:669–76.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Dixon R, Kahn D. Genetic regulation of biological nitrogen fixation. Nat Rev Microbiol. 2004;2:621–31.

CAS  PubMed  Article  Google Scholar 

Tang K, Jiao N, Liu K, Zhang Y, Li S. Distribution and functions of TonB-dependent transporters in marine bacteria and environments: implications for dissolved organic matter utilization. PLoS One. 2012;7:e41204.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Finzi-Hart JA, Pett-Ridge J, Weber PK, Popa R, Fallon SJ, Gunderson T, et al. Fixation and fate of C and N in the cyanobacterium Trichodesmium using nanometer-scale secondary ion mass spectrometry. Proc Natl Acad Sci USA 2009;106:6345–50.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Watzer B, Forchhammer K. Cyanophycin synthesis optimizes nitrogen utilization in the unicellular cyanobacterium Synechocystis sp. strain PCC 6803. Appl Environ Microbiol. 2018; https://doi.org/10.1128/AEM.01298-18.

Lindell D, Padan E, Post AF. Regulation of ntcA expression and nitrite uptake in the marine Synechococcus sp. strain WH 7803. J Bacteriol. 1998;180:1878–86.

CAS  PubMed  PubMed Central  Article  Google Scholar 

Tolonen AC, Aach J, Lindell D, Johnson ZI, Rector T, Steen R, et al. Global gene expression of Prochlorococcus ecotypes in response to changes in nitrogen availability. Mol Syst Biol. 2006; https://doi.org/10.1038/msb4100087.

Si F, Le Treut G, Sauls JT, Vadia S, Levin PA, Jun S. Mechanistic origin of cell-size control and homeostasis in bacteria. Curr Biol. 2019; https://doi.org/10.1016/j.cub.2019.04.062.

Chien A-C, Hill NS, Levin PA. Cell size control in bacteria. Curr Biol. 2012; https://doi.org/10.1016/j.cub.2012.02.032.

Muratore D, Boysen AK, Harke MJ, Becker KW, Casey JR, Coesel SN, et al. Complex marine microbial communities partition metabolism of scarce resources over the diel cycle. Nat Ecol Evol. 2022;6:218–29.

Hutchins DA, Boyd PW. Marine phytoplankton and the changing ocean iron cycle. Nat Clim Chang. 2016; https://doi.org/10.1038/nclimate3147.

Hutchins DA, Capone DG. The marine nitrogen cycle: new developments and global change. Nat Rev Microbiol. 2022;20:401–14.

This research was supported by U.S. National Science Foundation Biological Oceanography program grants OCE 1657757, OCE 1851222 to DAH, FXF, and EAW, OCE 2149837 to DAH and FXF, SCOR Working Group 149, as well as graduate student support from a USC Provost Fellowship to NY. We would also like to thank three anonymous reviewers who provided comments to improve this manuscript.

Present address: Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA

Department of Biological Sciences, University of Southern California, Los Angeles, CA, USA

Nina Yang, Yu-An Lin, Carlin A. Merkel, Michelle A. DeMers, Ping-Ping Qu, Eric A. Webb, Fei-Xue Fu & David A. Hutchins

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NY, F-FX, P-PQ, and DAH designed the experiment. NY carried out the experiment, with significant support from Y-AL, CAM, and MAD in monitoring cultures using cell-based growth rates and experimental maintenance. P-PQ and F-XF also contributed to experimental maintenance and support with physiological data analysis. NY collected large-volume samples, extracted RNA for transcriptomics analyses, and conducted differential gene expression analyses with support from P-PQ and EAW. NY wrote the manuscript with input from EAW and DAH. All authors reviewed and gave their approval for the final manuscript.

Correspondence to David A. Hutchins.

The authors declare no competing interests.

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Yang, N., Lin, YA., Merkel, C.A. et al. Molecular mechanisms underlying iron and phosphorus co-limitation responses in the nitrogen-fixing cyanobacterium Crocosphaera. ISME J (2022). https://doi.org/10.1038/s41396-022-01307-7

DOI: https://doi.org/10.1038/s41396-022-01307-7

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