Register      Login
Environmental Chemistry Environmental Chemistry Society
Environmental problems - Chemical approaches
RESEARCH ARTICLE

Arsenosugars and arsenolipids are formed simultaneously by the unicellular alga Dunaliella tertiolecta

Ronald A. Glabonjat https://orcid.org/0000-0003-3104-1940 A B C * , Elliott G. Duncan D , Frank Krikowa E , Kevin A. Francesconi A and William A. Maher E
+ Author Affiliations
- Author Affiliations

A Institute of Chemistry, NAWI Graz, University of Graz, Universitaetsplatz 1, 8010 Graz, Austria.

B Department of Environmental Health Sciences, Columbia University, New York, NY 10032, USA.

C NIEHS Center for Environmental Health in Northern Manhattan, Columbia University, New York, NY 10032, USA.

D Environmental Contaminants Group, Future Industries Institute, University of South Australia, Mawson Lakes Boulevard, Mawson Lakes, SA 5095, Australia.

E Biogeochemistry Group Research School of Earth Sciences, Australian National University, 2601, Australia.

* Correspondence to: rag2216@columbia.edu

Handling Editor: Kevin Wilkinson

Environmental Chemistry 19(4) 183-200 https://doi.org/10.1071/EN22043
Submitted: 2 May 2022  Accepted: 22 July 2022   Published: 30 September 2022

© 2022 The Author(s) (or their employer(s)). Published by CSIRO Publishing.

Environmental context. Arsenic is a globally distributed element, occurring in various chemical forms with toxicities ranging from harmless to highly toxic. We conducted 48-h cell culture experiments under batch and continuous conditions using the ubiquitous marine unicellular alga Dunaliella tertiolecta and evaluated the alga’s arsenic metabolome over time. We found that the alga first methylates the inorganic As taken up from the surrounding water, and then further metabolises the intermediate simultaneously into more complex organo-arsenic molecules like sugars and lipids. These time series experiments are valuable pieces in the puzzle of how algae bio-metabolise arsenic, and in our understanding of the global arsenic cycle.

Rationale. The uptake of arsenate by algae from oceanic waters and its transformation to arsenosugars and arsenolipids is well established, but the biosynthetic pathways remain largely unknown.

Methodology. We investigated these pathways by using time-series experiments over 48 h to follow the formation of organoarsenic species from arsenate-enriched medium (15 µg As L−1) by the unicellular alga Dunaliella tertiolecta cultured under batch and continuous culture conditions. We used complementary mass spectrometry methods for the determination and quantification of 14 arsenic species; an additional three species could be quantified but remained unidentified.

Results. The alga rapidly methylated the arsenate to dimethylarsinate (DMA), which then served as the precursor to arsenosugars and arsenolipids; the concentrations of these complex organoarsenicals increased throughout the experiments accompanied by a concomitant reduction in DMA concentrations. The pattern of compounds formed by the alga was similar for both batch and continuous cultures, but the concentrations were 2–3-fold higher in the continuous culture samples and the increases with time were much clearer.

Discussion. The data suggest that the arsenosugars and the arsenolipids were mostly formed simultaneously from DMA, although there was an indication that the arsenic phospholipids were at least partly also being formed from the arsenosugars. Overall, the data are consistent with a direct biosynthesis of DMA from arsenate by D. tertioleta, and thereafter a non-specific incorporation of DMA into commonly available alga metabolites encompassing various sugars and lipids.

Keywords: Arsenic speciation, bio-metabolism, cell culture, elemental analysis, high performance liquid chromatography, high-resolution MS, mass spectrometry, microalgae, phytoplankton.


References

Andreae MO, Klumpp D (1979). Biosynthesis and release of organoarsenic compounds by marine algae. Environmental Science & Technology 13, 738–741.
Biosynthesis and release of organoarsenic compounds by marine algae.Crossref | GoogleScholarGoogle Scholar |

Aoyama I, Okamura H (1993). Interactive toxic effect and bioconcentration between cadmium and chromium using continuous algal culture. Environmental Toxicology and Water Quality 8, 255–269.
Interactive toxic effect and bioconcentration between cadmium and chromium using continuous algal culture.Crossref | GoogleScholarGoogle Scholar |

Cannon JR, Edmonds JS, Francesconi KA, Raston CL, Saunders JB, Skelton BW, White AH (1981). Isolation, crystal structure and synthesis of arsenobetaine, a constituent of the western rock lobster, the dusky shark, and some samples of human urine. Australian Journal of Chemistry 34, 787–798.
Isolation, crystal structure and synthesis of arsenobetaine, a constituent of the western rock lobster, the dusky shark, and some samples of human urine.Crossref | GoogleScholarGoogle Scholar |

Challenger F (1945). Biological methylation. Chemical Reviews 36, 315–361.
Biological methylation.Crossref | GoogleScholarGoogle Scholar |

Cooney RV, Mumma RO, Benson AA (1978). Arsoniumphospholipid in algae. Proceedings of the National Academy of Sciences 75, 4262–4264.
Arsoniumphospholipid in algae.Crossref | GoogleScholarGoogle Scholar |

Droop MR (1974). The nutrient status of algal cells in continuous culture. Journal of the Marine Biological Association of the United Kingdom 54, 825–855.
The nutrient status of algal cells in continuous culture.Crossref | GoogleScholarGoogle Scholar |

Duncan E, Foster S, Maher W (2010). Uptake and metabolism of arsenate, methylarsonate and arsenobetaine by axenic cultures of the phytoplankton Dunaliella tertiolecta. Botanica Marina 53, 377–386.
Uptake and metabolism of arsenate, methylarsonate and arsenobetaine by axenic cultures of the phytoplankton Dunaliella tertiolecta.Crossref | GoogleScholarGoogle Scholar |

Duncan EG, Maher WA, Foster SD, Krikowa F (2013a). The influence of arsenate and phosphate exposure on arsenic uptake, metabolism and species formation in the marine phytoplankton Dunaliella tertiolecta. Marine Chemistry 157, 78–85.
The influence of arsenate and phosphate exposure on arsenic uptake, metabolism and species formation in the marine phytoplankton Dunaliella tertiolecta.Crossref | GoogleScholarGoogle Scholar |

Duncan EG, Maher WA, Foster SD, Krikowa F (2013b). Influence of culture regime on arsenic cycling by the marine phytoplankton Dunaliella tertiolecta and Thalassiosira pseudonana. Environmental Chemistry 10, 91–101.
Influence of culture regime on arsenic cycling by the marine phytoplankton Dunaliella tertiolecta and Thalassiosira pseudonana.Crossref | GoogleScholarGoogle Scholar |

Duncan EG, Maher WA, Foster SD, Mikac KM, Krikowa F (2014). The influence of bacteria on the arsenic species produced by laboratory cultures of the marine phytoplankton Dunaliella tertiolecta. Journal of Applied Phycology 26, 2129–2134.
The influence of bacteria on the arsenic species produced by laboratory cultures of the marine phytoplankton Dunaliella tertiolecta.Crossref | GoogleScholarGoogle Scholar |

Duncan EG, Maher WA, Foster SD (2015). Contribution of arsenic species in unicellular algae to the cycling of arsenic in marine ecosystems. Environmental Science & Technology 49, 33–50.
Contribution of arsenic species in unicellular algae to the cycling of arsenic in marine ecosystems.Crossref | GoogleScholarGoogle Scholar |

Edmonds JS, Francesconi KA (1981). Arseno-sugars from brown kelp (Ecklonia radiata) as intermediates in cycling of arsenic in a marine ecosystem. Nature 289, 602–604.
Arseno-sugars from brown kelp (Ecklonia radiata) as intermediates in cycling of arsenic in a marine ecosystem.Crossref | GoogleScholarGoogle Scholar |

Edmonds JS, Francesconi KA (1983). Arsenic-containing ribofuranosides: isolation from brown kelp Ecklonia radiata and nuclear magnetic resonance spectra. Journal of the Chemical Society, Perkin Transactions 1, 2375–2382.
Arsenic-containing ribofuranosides: isolation from brown kelp Ecklonia radiata and nuclear magnetic resonance spectra.Crossref | GoogleScholarGoogle Scholar |

Edmonds JS, Francesconi KA, Cannon JR, Raston CL, Skelton BW, White AH (1977). Isolation, crystal structure and synthesis of arsenobetaine, the arsenical constituent of the western rock lobster panulirus longipes cygnus George. Tetrahedron Letters 18, 1543–1546.
Isolation, crystal structure and synthesis of arsenobetaine, the arsenical constituent of the western rock lobster panulirus longipes cygnus George.Crossref | GoogleScholarGoogle Scholar |

Erb TJ, Kiefer P, Hattendorf B, Günther D, Vorholt JA (2012). GFAJ-1 is an arsenate-resistant, phosphate-dependent organism. Science 337, 467–470.
GFAJ-1 is an arsenate-resistant, phosphate-dependent organism.Crossref | GoogleScholarGoogle Scholar |

Foster S, Thomson D, Maher W (2008). Uptake and metabolism of arsenate by anexic cultures of the microalgae Dunaliella tertiolecta and Phaeodactylum tricornutum. Marine Chemistry 108, 172–183.
Uptake and metabolism of arsenate by anexic cultures of the microalgae Dunaliella tertiolecta and Phaeodactylum tricornutum.Crossref | GoogleScholarGoogle Scholar |

Francesconi KA, Edmonds JS, Stick RV (1992). Arsenic compounds from the kidney of the giant clam Tridacna maxima: isolation and identification of an arsenic-containing nucleoside. Journal of the Chemical Society, Perkin Transactions 1, 1349–1357.
Arsenic compounds from the kidney of the giant clam Tridacna maxima: isolation and identification of an arsenic-containing nucleoside.Crossref | GoogleScholarGoogle Scholar |

Francesconi KA, Hunter DA, Bachmann B, Raber G, Goessler W (1999). Uptake and transformation of arsenosugars in the shrimp Crangon crangon. Applied Organometallic Chemistry 13, 669–679.
Uptake and transformation of arsenosugars in the shrimp Crangon crangon.Crossref | GoogleScholarGoogle Scholar |

García-Salgado S, Raber G, Raml R, Magnes C, Francesconi KA (2012). Arsenosugar phospholipids and arsenic hydrocarbons in two species of brown macroalgae. Environmental Chemistry 9, 63–66.
Arsenosugar phospholipids and arsenic hydrocarbons in two species of brown macroalgae.Crossref | GoogleScholarGoogle Scholar |

Geiszinger A, Goessler W, Pedersen SN, Francesconi KA (2001). Arsenic biotransformation by the brown macro alga Fucus serratus. Environmental Toxicology and Chemistry 20, 2255–2262.
Arsenic biotransformation by the brown macro alga Fucus serratus.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Raber G, Jensen KB, Ehgartner J, Francesconi KA (2014). Quantification of arsenolipids in the certified reference material NMIJ 7405-a (Hijiki) using HPLC/mass spectrometry after chemical derivatization. Analytical Chemistry 86, 10282–10287.
Quantification of arsenolipids in the certified reference material NMIJ 7405-a (Hijiki) using HPLC/mass spectrometry after chemical derivatization.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Raber G, Jensen KB, Guttenberger N, Zangger K, Francesconi KA (2017a). A 2-O-methylriboside unknown outside the RNA world contains arsenic. Angewandte Chemie International Edition 56, 11963–11965.
A 2-O-methylriboside unknown outside the RNA world contains arsenic.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Raber G, Van Mooy BAS, Francesconi KA (2017b). Arsenobetaine in seawater: Depth profiles from selected sites in the North Atlantic. Environmental Science & Technology 52, 522–530.
Arsenobetaine in seawater: Depth profiles from selected sites in the North Atlantic.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Ehgartner J, Duncan EG, Raber G, Jensen KB, Krikowa F, Maher WA, Francesconi KA (2018). Arsenolipid biosynthesis by the unicellular alga Dunaliella tertiolecta is influenced by As/P ratio in culture experiments. Metallomics 10, 145–153.
Arsenolipid biosynthesis by the unicellular alga Dunaliella tertiolecta is influenced by As/P ratio in culture experiments.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Raber G, Jensen KB, Schubotz F, Boyd ES, Francesconi KA (2019). Origin of arsenolipids in sediments from Great Salt Lake. Environmental Chemistry 16, 303–311.
Origin of arsenolipids in sediments from Great Salt Lake.Crossref | GoogleScholarGoogle Scholar |

Glabonjat RA, Blum JS, Miller LG, Webb SM, Stolz JF, Francesconi KA, Oremland RS (2020). Arsenolipids in Cultured Picocystis strain ML and their occurrence in biota and sediment from Mono Lake, California. Life 10, 93
Arsenolipids in Cultured Picocystis strain ML and their occurrence in biota and sediment from Mono Lake, California.Crossref | GoogleScholarGoogle Scholar |

Guillard RRL, Ryther JH (1962). Studies of marine planktonic diatoms: I. Cyclotella Nana Hustedt, and Detonula Confervacea (Cleve) Gran. Canadian Journal of Microbiology 8, 229–239.
Studies of marine planktonic diatoms: I. Cyclotella Nana Hustedt, and Detonula Confervacea (Cleve) Gran.Crossref | GoogleScholarGoogle Scholar |

Morita M, Shibata Y (1988). Isolation and identification of arseno-lipid from a brown alga, Undaria pinatifisa (Wakame). Chemosphere 17, 1147–1152.
Isolation and identification of arseno-lipid from a brown alga, Undaria pinatifisa (Wakame).Crossref | GoogleScholarGoogle Scholar |

Narukawa T, Raber G, Itoh N, Inagaki K (2020). A new candidate reference material for inorganic arsenic and arsenosugars in Hijiki seaweed: first results from an inter-laboratory study. Analytical Sciences 36, 233–239.
A new candidate reference material for inorganic arsenic and arsenosugars in Hijiki seaweed: first results from an inter-laboratory study.Crossref | GoogleScholarGoogle Scholar |

Nriagu JO (1994) ‘Arsenic in the Environment, Part 2: Human Health and Ecosystem Effects.’ (Wiley: New York, NY, USA)

Okay OS, Gaines A, Davie AM (2003). The growth of continuous cultures of the phytoplankton Phaeodactylum tricornutum. Turkish Journal of Engineering and Environmental Sciences 27, 145–155.

Pétursdóttir ÁH, Fletcher K, Gunnlaugsdóttir H, Krupp E, Küpper FC, Feldmann J (2016). Environmental effects on arsenosugars and arsenolipids in Ectocarpus (Phaeophyta). Environmental Chemistry 13, 21–33.
Environmental effects on arsenosugars and arsenolipids in Ectocarpus (Phaeophyta).Crossref | GoogleScholarGoogle Scholar |

Raber G, Raml R, Goessler W, Francesconi KA (2010). Quantitative speciation of arsenic compounds when using organic solvent gradients in HPLC-ICPMS. Journal of Analytical Atomic Spectrometry 25, 570–576.
Quantitative speciation of arsenic compounds when using organic solvent gradients in HPLC-ICPMS.Crossref | GoogleScholarGoogle Scholar |

Reaves ML, Sinha S, Rabinowitz JD, Kruglyak L, Redfield RJ (2012). Absence of detectable arsenate in DNA from arsenate-grown GFAJ-1 cells. Science 337, 470–473.
Absence of detectable arsenate in DNA from arsenate-grown GFAJ-1 cells.Crossref | GoogleScholarGoogle Scholar |

Řezanka T, Nedbalová L, Barcytė D, Vítová M, Sigler K (2019). Arsenolipids in the green alga Coccomyxa (Trebouxiophyceae, Chlorophyta). Phytochemistry 164, 243–251.
Arsenolipids in the green alga Coccomyxa (Trebouxiophyceae, Chlorophyta).Crossref | GoogleScholarGoogle Scholar |

Taleshi MS, Seidler-Egdal RK, Jensen KB, Schwerdtle T, Francesconi KA (2014). Synthesis and characterization of arsenolipids: naturally occurring arsenic compounds in fish and algae. Organometallics 33, 1397–1403.
Synthesis and characterization of arsenolipids: naturally occurring arsenic compounds in fish and algae.Crossref | GoogleScholarGoogle Scholar |

Wolfe-Simon F, Blum JS, Kulp TR, Gordon GW, Hoeft SE, Pett-Ridge J, Stolz JF, Webb SM, Weber PK, Davies PCW, Anbar AD, Oremland RS (2011). A bacterium that can grow by using arsenic instead of phosphorus. Science 332, 1163–1166.
A bacterium that can grow by using arsenic instead of phosphorus.Crossref | GoogleScholarGoogle Scholar |

Xue X-M, Xiong C, Yoshinaga M, Rosen B, Zhu Y-G (2021). The enigma of environmental organoarsenicals: insights and implications. Critical Reviews in Environmental Science and Technology 52, 1–28.
The enigma of environmental organoarsenicals: insights and implications.Crossref | GoogleScholarGoogle Scholar |

Zhang S-Y, Sun G-X, Yin X-X, Rensing C, Zhu Y-G (2013). Biomethylation and volatilization of arsenic by the marine microalgae Ostreococcus tauri. Chemosphere 93, 47–53.
Biomethylation and volatilization of arsenic by the marine microalgae Ostreococcus tauri.Crossref | GoogleScholarGoogle Scholar |

Zhu Y-G, Xue X-M, Kappler A, Rosen BP, Meharg AA (2017). Linking genes to microbial biogeochemical cycling: lessons from arsenic. Environmental Science & Technology 51, 7326–7339.
Linking genes to microbial biogeochemical cycling: lessons from arsenic.Crossref | GoogleScholarGoogle Scholar |