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25th International Meeting on Organic Geochemistry IMOG 2011

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Bacteria number ml-1 Bacteria number ml-1 1.2 E+07<br />

1.0 E+07<br />

8.0 E+06<br />

6.0 E+06<br />

4.0 E+06<br />

2.0 E+06<br />

O-69<br />

Role of photooxidative processes in senescent phytoplankt<strong>on</strong><br />

cells and attached bacteria in the preservati<strong>on</strong> of organic matter<br />

Morgan Petit 1 , Richard Sempere 1 , Stuart G. Wakeham 2 , John K. Volkman 3 , Frédéric<br />

Vaultier 1 , Jean-François R<strong>on</strong>tani 1<br />

1 Laboratoire de Microbiologie Géochimie et Ecologie Marines (LMGEM -UMR 6117), Marseille, France,<br />

2 Skidaway Institute of Oceanography, Savannah, United States of America, 3 CSIRO Marine and<br />

Atmospheric Research, Hobart, Australia (corresp<strong>on</strong>ding author:jean-francois.r<strong>on</strong>tani@univmed.fr)<br />

Visible-light-induced photosensitizati<strong>on</strong> processes are<br />

intense during the senescence of phytoplankt<strong>on</strong> cells.<br />

These processes mainly involve singlet oxygen ( 1 O2)<br />

and act <strong>on</strong> most of the unsaturated lipid comp<strong>on</strong>ents<br />

(including sterols, unsaturated fatty acids and the<br />

chlorophyll phytyl side-chain) of these organisms. The<br />

effects of photooxidati<strong>on</strong>, however, may go bey<strong>on</strong>d<br />

the algal cellular lipids that are initially affected. If the<br />

photochemical producti<strong>on</strong> of<br />

1 O2 exceeds the<br />

quenching capacity of the photoprotective system,<br />

this excited form of oxygen can migrate outside the<br />

chloroplasts and induce degradati<strong>on</strong> of comp<strong>on</strong>ents<br />

of attached heterotrophic bacteria [1]. Cellular<br />

damage resulting from the transfer of high amounts of<br />

1<br />

O2 to heterotrophic bacteria may be significant due<br />

to the lack of efficient photoprotective and antioxidant<br />

systems in these microorganisms. This transfer may<br />

thus affect the preservati<strong>on</strong> of algal material in the<br />

marine envir<strong>on</strong>ment.<br />

In order to check this hypothesis, n<strong>on</strong>-axenic cells of<br />

Emiliania huxleyi were grown under c<strong>on</strong>secutive<br />

irradiance regimes: light and dark, dark and light and<br />

dark.<br />

Dark incubati<strong>on</strong><br />

Return<br />

to light<br />

0<br />

0<br />

0 2 4 6 8 10 12 14 16 18 20<br />

Sampling day<br />

7.0<br />

6.0<br />

5.0<br />

4.0<br />

3.0<br />

2.0<br />

1.0<br />

Fig1. Evoluti<strong>on</strong> of bacterial number (diam<strong>on</strong>ds) and of<br />

the amounts of vaccenic acid oxidati<strong>on</strong> products<br />

(open boxes) during the experiment<br />

Bacterial counts showed a str<strong>on</strong>g increase during the<br />

incubati<strong>on</strong> under darkness and a significant decrease<br />

Vaccenic oxidati<strong>on</strong> products (ng ml-1 Vaccenic oxidati<strong>on</strong> products (ng ml ) -1 )<br />

after return to light (Fig. 1). The simultaneous<br />

increase in the amount of oxidati<strong>on</strong> products resulting<br />

from the attack by singlet oxygen <strong>on</strong> vaccenic acid (a<br />

typical bacterial fatty acid) and decrease in bacterial<br />

numbers observed after the return to light (Fig. 1) fits<br />

nicely with this hypothesis.<br />

In order to better understand unexpected abundances<br />

of labile OM at depth in the Equatorial Pacific we reinvestigated<br />

lipids in suspended and sinking<br />

particulate organic matter (POM) samples that had<br />

been analyzed previously [2]. Biodegradati<strong>on</strong> was<br />

more intense in sinking POM than suspended POM.<br />

We could attribute this difference to an efficient<br />

transfer of singlet oxygen from suspended and<br />

senescent phytoplankt<strong>on</strong> cells to associated bacteria<br />

and subsequent inhibiti<strong>on</strong> of heterotrophic<br />

degradati<strong>on</strong> [3]. On the other hand, we speculate that<br />

an abundance of charged mineral surfaces, such as<br />

siliceous diatom frustules or carb<strong>on</strong>aceous coccoliths<br />

in sinking particles, may reduce the lifetime of 1 O2<br />

and allow for enhanced bacterial growth and<br />

biodegradati<strong>on</strong> in sinking particles compared to<br />

suspended particles [3]. It thus seems that there is a<br />

direct link between the photooxidati<strong>on</strong> state of lipids of<br />

senescent phytoplankt<strong>on</strong>ic cells in suspended<br />

particles and their recalcitrance towards biotic<br />

degradati<strong>on</strong>. These results could explain some<br />

previous observati<strong>on</strong>s showing that in northeast<br />

Pacific Ocean sinking particles c<strong>on</strong>tain a more active<br />

bacterial community than suspended particles [4].<br />

[1] R<strong>on</strong>tani J.-F., M. Koblizek, B. Beker, P. B<strong>on</strong>in, and<br />

Z. Kolber. 2003. Lipids 38: 1085-1092.<br />

[2] Wakeham S.G., J.I. Hedges, C. Lee, M.L.<br />

Peters<strong>on</strong>, and P.J. Hernes. 1997. Deep-Sea Res. II<br />

44: 2131-2162.<br />

[3] R<strong>on</strong>tani J.-F., N. Zabeti, S.G. Wakeham. 2010<br />

Limnol. Oceanogr. 56: 333-346.<br />

[4] Karl, D. M., and G. A. Knauer. 1984. Deep-Sea<br />

Res. 31: 221-243.<br />

130

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