The influence of arsenate and phosphate exposure on arsenic uptake, metabolism and species formation in the marine phytoplankton dunaliella tertiolecta

Marine Chemistry

Volumn 157, Issue , 2013, Pages 78-85

  Duncan, Elliott G ^a   Maher, William A ^a   Foster, Simon D ^a   Krikowa, Frank ^a  

^a UNIVERSITY OF CANBERRA   (Australia)

Author keywords

Arsenate; Arsenic cycling; Batch phytoplankton cultures; Dunaliella tertiolecta; Marine phytoplankton; Nutrient cycling; Phosphate

Indexed keywords

ARSENATE; ARSENIC; BIOLOGICAL UPTAKE; CHEMICAL COMPOSITION; CONCENTRATION (COMPOSITION); LIPID; MARINE ENVIRONMENT; METABOLISM; NUTRIENT CYCLING; PHOSPHATE; PHYTOPLANKTON; POLLUTION EXPOSURE; SOLUBILIZATION;

DUNALIELLA TERTIOLECTA;

EID: 84884540132     PISSN: 03044203     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.marchem.2013.08.004     Document Type: Article

References (55)

1. Andreae M.O. Distribution and speciation of arsenic in natural waters and some marine algae. Deep-Sea Res. 1978, 25:391-402.
2. Baldwin S., Deaker M., Maher W. Low volume microwave digestion of marine biological tissues for the measurement of trace elements. Analyst 1994, 119:1701-1704.
3. Beardall J., et al. A comparison of methods for detection of phosphate limitation in microalgae. Aquat. Sci. 2001, 63(1):107-121.
4. Bellinger B.J., Van Mooy B.A. Nonphosphorus lipids in periphyton reflect available nutrients in the Florida Everglades, USA. J. Phycol. 2012, 48(2):303-311.
5. Button D.K., Dunker S.S., Morse M.L. Continuous culture of Rhodotorula rubra: kinetics of phosphate-arsenate uptake, inhibition, and phosphate-limited growth. J. Bacteriol. 1973, 113(2):599-611.
6. Cannon J., et al. Isolation, crystal structure and synthesis of arsenobetaine, a constituent of the western rock lobster, the dusky shark, and some samples of human urine. Aust. J. Chem. 1981, 34(4):787-798.
7. Challenger F. Biological methylation. Chem. Rev. 1945, 36:315-361.
8. Cotner-Jr J.B., Wetzel R.G. Uptake of dissolved inorganic and organic phosphorus compounds by phytoplankton and bacterioplankton. Limnol. Oceanogr. 1992, 37(2):232-243.
9. Cullen W.R., Harrison L.G., Li H., Hewitt G. Bioaccumulation and excretion of arsenic compounds by a marine unicellular alga, Polyphysa peniculus. Appl. Organomet. Chem. 1994, 8:313-324.
10. Deaker M., Maher W. Determination of arsenic in arsenic compounds and marine biological tissues using low volume microwave digestion and electrothermal atomic absorption spectrometry. J. Anal. At. Spectrom. 1999, 14:1193-1207.
11. Downing J.A. Marine nitrogen: phosphorus stoichiometry and the global N:P cycle. Biogeochemistry 1997, 37:237-252.
12. Droop M.R. The nutrient status of algal cells in batch culture. J. Mar. Biol. Assoc. UK 1975, 55:541-555.
13. Duncan E., Foster S., Maher W. Uptake and metabolism of arsenate, methylarsonate and arsenobetaine by axenic cultures of the phytoplankton Dunaliella tertiolecta. Bot. Mar. 2010, 53:377-386.
14. Duncan E.G., Maher W.A., Foster S.D., Krikowa F. Influence of culture regime on arsenic cycling by the marine phytoplankton Dunaliella tertiolecta and Thalassiosira pseudonana. Environ. Chem. 2013, 10(2):91-101.
15. Edmonds J.S., Francesconi K.A. Organoarsenic compounds in the marine environment. Organometallic Compounds in the Environment 2003, 196-222. John Wiley and Sons, New York. P.J. Craig (Ed.).
16. Edmonds J.S., Francesconi K.A., Hansen J.A. Dimethyloxarsylethanol from anaerobic decomposition of brown kelp (Ecklonia radiata): a likely precursor of arsenobetaine in marine fauna. Experientia 1982, 38:643-644.
17. Folch J., Lees M., Sloane Stanley G.H. A simple method for the isolation and purification of total lipids from animal tissue. J. Biol. Chem. 1957, 226:497-509.
18. Foster S., Maher W., Krikowa F., Apte S. A microwave assisted sequential extraction of water and dilute acid soluble arsenic species from marine plant and animal tissues. Talanta 2007, 71:537-549.
19. Foster S., Maher W., Krikowa F. Changes in proportions of arsenic species within an Ecklonia radiata food chain. Environ. Chem. 2008, 5:176-183.
20. Foster S., Thomson D., Maher W. Uptake and metabolism of arsenate by anexic cultures of the microalgae Dunaliella tertiolecta and Phaeodactylum tricornutum. Mar. Chem. 2008, 108:172-183.
21. Francesconi K.A., Edmonds J.S., Stick R.V. Accumulation of arsenic in yelloweye mullet (Aldrichetta forsteri) following oral administration of organoarsenic compounds and arsenate. Sci. Total. Environ. 1989, 79(1):59-67.
22. García-Salgado S., Raber G., Raml R., Magnes C., Francesconi K.A. Arsenosugar phospholipids and arsenic hydrocarbons in two species of brown macroalgae. Environ. Chem. 2012, 9(1):63-66.
23. Guillard R.R.L., Ryther J.H. Studies on planktonic diatoms. I. Cyclotela nana (Hustedt) and Detonula confervacea (CleveGran.). Can. J. Microbiol. 1962, 8:229-239.
24. Guschina I.A., Harwood J.L. Lipids and lipid metabolism in eukaryotic algae. Prog. Lipid Res. 2006, 45:160-186.
25. Harrison P.J., Thompson P.A., Calderwood G.S. Effects of nutrient and light limitation on the biochemical composition of phytoplankton. J. Appl. Phycol. 1990, 2:45-56.
26. Hellweger F., Farley K.J., Lall U., Di Toro D.M. Greedy algae reduce arsenate. Limnol. Oceanogr. 2003, 48:2275-2288.
27. Khotimchenko S.V., Yakovleva I.M. Lipid composition of the red alga Tichocarpus crinitus exposed to different levels of photon irradiance. Phytochemistry 2005, 66:73-79.
28. Kirby J., Maher W., Ellwood M., Krikowa F. Arsenic species determination in biological tissues by HPLC-ICP-MS and HPLC-HG-ICP-MS. Aust. J. Chem. 2004, 57:957-966.
29. Lombardi A.T., Wangersky P.J. Influence of phosphorus and silicon on lipid class production by the marine diatom Chaetoceros gracilis grown in turbidostat cage cultures. Mar. Ecol. Prog. Ser. 1991, 77:39-47.
30. Lombardi A.T., Wangersky P.J. Particulate lipid class composition of three marine phytoplankters Chaetoceros gracilis, Isochrysis galbana (Tahiti) and Dunaliella tertiolecta grown in batch cultures. Hydrobiologia 1995, 306:1-6.
31. Madsen A.D., Goessler W., Pedersen S.N., Francesconi K.A. Characterization of an algal extract by HPLC-ICP-MS and LC-electrospray MS for use in arsenosugar speciation studies. J. Anal. At. Spectrom. 2000, 15(6).
32. Maher W., et al. Measurement of trace metals and phosphorus in marine animal and plant tissues by low volume microwave digestion and ICPMS. J. Anal. At. Spectrom. 2001, 22:361-369.
33. Maher W., et al. Determination of total phosphorus and nitrogen in turbid waters by oxidation with alkaline potassium peroxodisulfate and low pressure microwave digestion, autoclave heating or the use of closed vessels in a hot water bath: comparison with Kjeldahl digestion. Anal. Chim. Acta 2002, 463:283-293.
34. Maher W., Foster S., Krikowa F. Arsenic species in Australian temperate marine food chains. Mar. Freshw. Res. 2009, 60:885-892.
35. Meharg A.A., Macnair M.R. An altered phosphate uptake system in arsenate-tolerant Holcus lanatus L. New Phytol. 1990, 116:29-35.
36. Merijanian A., Zingaro R.A. Arsine oxides. Inorg. Chem. 1966, 5(2):187-191.
37. Minhas R., Forsyth D.S., Dawson B. Synthesis and characterization of arsenobetaine and arsenocholine derivatives. Appl. Organomet. Chem. 1998, 12(8-9):635-641.
38. Momplaisir G.M., Blais J.S., Quinteiro M., Marshall W.D. Determination of arsenobetaine, arsenocholine, and tetramethylarsonium cations in seafoods and human urine by high-performance liquid chromatography-thermochemical hydride generation-atomic absorption spectrometry. J. Agric. Food Chem. 1991, 39(8):1448-1451.
39. Neff J.M. Ecotoxicology of arsenic in the marine environment. Environ. Toxicol. Chem. 1997, 16(5):917-927.
40. Oremland R.S., Stolz J.F. The ecology of arsenic. Science 2003, 300:939-944.
41. Perry M.J. Phosphate utilization by an oceanic diatom in phosphorus-limited chemostat culture and in the oligotrophic waters of the central North Pacific. Limnol. Oceanogr. 1976, 21(1):88-107.
42. Raml R., Goessler W., Francesconi K.A. Improved chromatographic separation of thio-arsenic compounds by reversed-phase high performance liquid chromatography-inductively coupled plasma mass spectrometry. J. Chromatogr. A 2006, 1128(1-2):164-170.
43. Rothstein A., Donovan K. Interaction of arsenate with the phosphate-transporting system of yeast. J. Gen. Physiol. 1963, 46:1075-1085.
44. Sanders J.G., Windom H.L. The uptake and reduction of arsenic species by marine algae. Estuar. Coast. Mar. Sci. 1980, 10:555-567.
45. Sanders J.G., Osman R.W., Reidel G.F. Pathways of arsenic uptake and incorporation in estuarine phytoplankton and the filterfeeding invertebrates Eurytemora affinis, Balanus improvisus and Crassostrea virginica. Mar. Biol. 1989, 103:319-325.
46. Suzumura M. Phospholipids in marine environments: a review. Talanta 2005, 66:422-434.
47. Takamura O., Fuse H., Murakami K., Kamimura K., Yamaoka Y. Uptake and reduction of arsenate by Dunaliella sp. Appl. Organomet. Chem. 1996, 10:753-756.
48. Thomson D., Maher W., Foster S. Arsenic and selected elements in inter-tidal and estuarine marine algae, south-east coast, NSW, Australia. Appl. Organomet. Chem. 2007, 21(6):396-411.
49. Tukai R., Maher W.A., McNaught I.J., Ellwood M.J., Coleman M. Occurrence and chemical form of arsenic in marine macroalgae from the east coast of Australia. Mar. Freshw. Res. 2002, 53(6):971-980.
50. Van Mooy B.A.S., et al. Phytoplankton in the ocean use non-phosphorus lipids in response to phosphorus scarcity. Nature 2009, 458:69-72.
51. Wolfe-Simon F., et al. A bacterium that can grow by using arsenic instead of phosphorus. Science 2011, 332:1163-1166.
52. Wrench J.J., Addison R.F. Reduction, methylation, and incorporation of arsenic into lipids by the marine phytoplankton Dunaliella tertiolecta. Can. J. Fish. Aquat. Sci. 1981, 38:518-523.
53. Wurl O., Zimmer L., Cutter G.A. Arsenic and phosphorus biogeochemistry in the ocean: arsenic species as proxies for P-limitation. Limnol. Oceanogr. 2013, 58(2):729-740.
54. Yamaoka Y., Takimura O., Fuse H., Kamimura K. Accumulation of arsenic and selenium by Dunaliella sp. Appl. Organomet. Chem. 1990, 4:261-264.
55. Yamaoka Y., Takamura O., Fuse H., Murakami K. Effect of glutathione on arsenic accumulation by Dunaliella salina. Appl. Organomet. Chem. 1999, 13:89-94.