Sulfolipids dramatically decrease phosphorus demand by picocyanobacteria in oligotrophic marine environments.

There is growing evidence that dissolved phosphorus can regulate planktonic production in the oceans' subtropical gyres, yet there is little quantitative information about the biochemical fate of phosphorus in planktonic communities. We observed in the North Pacific Subtropical Gyre (NPSG) that the synthesis of membrane lipids accounted for 18-28% of the phosphate (PO4(3-)) taken up by the total planktonic community. Paradoxically, Prochlorococcus, the cyanobacterium that dominates NPSG phytoplankton, primarily synthesizes sulfoquinovosyldiacylglycerol (SQDG), a lipid that contains sulfur and sugar instead of phosphate. In axenic cultures of Prochlorococcus, it was observed that <1% of the total PO4(3-) uptake was incorporated into membrane lipids. Liquid chromatography/mass spectrometry of planktonic lipids in the NPSG confirmed that SQDG was the dominant membrane lipid. Furthermore, the analyses of SQDG synthesis genes from the Sargasso Sea environmental genome showed that the use of sulfolipids in subtropical gyres was confined primarily to picocyanobacteria; no sequences related to known heterotrophic bacterial SQDG lineages were found. This biochemical adaptation by Prochlorococcus must be a significant benefit to these organisms, which compete against phospholipid-rich heterotrophic bacteria for PO4(3-). Thus, evolution of this "sulfur-for-phosphorus" strategy set the stage for the success of picocyanobacteria in oligotrophic environments and may have been a major event in Earth's early history when the relative availability of sulfate and PO4(3-) were significantly different from today's ocean.

[1]  P. Quay,et al.  Experimental determination of the organic carbon flux from open-ocean surface waters , 1997, Nature.

[2]  H. Ducklow,et al.  Multiyear increases in dissolved organic matter inventories at Station ALOHA in the North Pacific Subtropical Gyre , 2002 .

[3]  D. Kirchman Microbial ecology of the oceans , 2008 .

[4]  S. Chisholm,et al.  Elemental composition of marine Prochlorococcus and Synechococcus: Implications for the ecological stoichiometry of the sea , 2003 .

[5]  Ricardo M Letelier,et al.  The role of nitrogen fixation in biogeochemical cycling in the subtropical North Pacific Ocean , 1997, Nature.

[6]  D. Gompertz Microbial Lipids , 1967, Nature.

[7]  B. V. Van Mooy,et al.  Relationship between bacterial community structure, light, and carbon cycling in the eastern subarctic North Pacific , 2004 .

[8]  N. Sato Roles of the acidic lipids sulfoquinovosyl diacylglycerol and phosphatidylglycerol in photosynthesis: their specificity and evolution , 2004, Journal of Plant Research.

[9]  J. LaRoche,et al.  Estimating the Growth Rate of Slowly Growing Marine Bacteria from RNA Content , 1993, Applied and environmental microbiology.

[10]  A. Knap,et al.  Elemental C, N, and P cell content of individual bacteria collected at the Bermuda Atlantic Time‐series Study (BATS) site , 2002 .

[11]  E. Boyle,et al.  Phosphate depletion in the western North Atlantic Ocean. , 2000, Science.

[12]  Lisa R. Moore,et al.  Utilization of different nitrogen sources by the marine cyanobacteria Prochlorococcus and Synechococcus , 2002 .

[13]  E. Ingall,et al.  Concentrations of lipid phosphorus and its abundance in dissolved and particulate organic phosphorus in coastal seawater , 2001 .

[14]  J. Waterbury,et al.  Biochemical composition and short term nutrient incorporation patterns in a unicellular marine cyanobacterium,Synechococcus(WH7803)1 , 1984 .

[15]  S. Wakeham,et al.  Molecular indicators of diagenetic status in marine organic matter , 1997 .

[16]  Sallie W. Chisholm,et al.  Resolution of Prochlorococcus and Synechococcus Ecotypes by Using 16S-23S Ribosomal DNA Internal Transcribed Spacer Sequences , 2002, Applied and Environmental Microbiology.

[17]  David M. Karl,et al.  A Sea of Change: Biogeochemical Variability in the North Pacific Subtropical Gyre , 1999, Ecosystems.

[18]  D. Karl,et al.  Phosphorus dynamics in the North Pacific subtropical gyre , 2000 .

[19]  Donald E. Canfield,et al.  Ocean productivity before about 1.9 Gyr ago limited by phosphorus adsorption onto iron oxides , 2002, Nature.

[20]  A. Paytan,et al.  Selective phosphorus regeneration of sinking marine particles: evidence from 31P-NMR , 2003 .

[21]  P. Siegenthaler,et al.  Lipids in Photosynthesis: Structure, Function and Genetics , 1998, Advances in Photosynthesis and Respiration.

[22]  P. Raimbault,et al.  Does competition for nanomolar phosphate supply explain the predominance of the cyanobacterium Synechococcus? , 2002 .

[23]  Manesh Shah,et al.  Genome divergence in two Prochlorococcus ecotypes reflects oceanic niche differentiation , 2003, Nature.

[24]  J. Smit,et al.  Woodsholea maritima gen. nov., sp. nov., a marine bacterium with a low diversity of polar lipids. , 2004, International journal of systematic and evolutionary microbiology.

[25]  Carlos M. Duarte,et al.  Respiration in the open ocean , 2002, Nature.

[26]  C. Bauer,et al.  Molecular evidence for the early evolution of photosynthesis. , 2000, Science.

[27]  Frede Thingstad,et al.  Elemental composition of single cells of various strains of marine Prochlorococcus and Synechococcus using X‐ray microanalysis , 2003 .

[28]  M. Cottrell,et al.  Aerobic Anoxygenic Phototrophic Bacteria in the Mid-Atlantic Bight and the North Pacific Gyre , 2006, Applied and Environmental Microbiology.

[29]  D. Scanlan,et al.  Dynamics of community structure and phosphate status of picocyanobacterial populations in the Gulf of Aqaba, Red Sea , 2005 .

[30]  R. Bidigare,et al.  Long-term changes in plankton community structure and productivity in the North Pacific Subtropical Gyre: The domain shift hypothesis , 2001 .

[31]  R. Benner,et al.  Composition and cycling of marine organic phosphorus , 2001 .

[32]  Hans-Peter Schertl,et al.  Geochim. cosmochim. acta , 1989 .

[33]  D. Canfield,et al.  Calibration of Sulfate Levels in the Archean Ocean , 2002, Science.

[34]  O. White,et al.  Environmental Genome Shotgun Sequencing of the Sargasso Sea , 2004, Science.

[35]  N. Kawasaki,et al.  P-limitation of respiration in the Sargasso Sea and uncoupling of bacteria from P-regeneration in size-fractionation experiments , 2003 .

[36]  D. White,et al.  Determination of the sedimentary microbial biomass by extractible lipid phosphate , 2004, Oecologia.

[37]  Kemp,et al.  Small ribosomal RNA content in marine Proteobacteria during non-steady-state growth. , 1999, FEMS microbiology ecology.

[38]  R. Summons,et al.  Intact polar membrane lipids in prokaryotes and sediments deciphered by high-performance liquid chromatography/electrospray ionization multistage mass spectrometry--new biomarkers for biogeochemistry and microbial ecology. , 2004, Rapid communications in mass spectrometry : RCM.

[39]  J. Fuhrman,et al.  Wide‐ranging abundances of aerobic anoxygenic phototrophic bacteria in the world ocean revealed by epifluorescence microscopy and quantitative PCR , 2005 .