Deep-Sea
Genome/Proteome
Microbial sulfate reduction is an important
process in deep-sea habitats. Furthermore deep-sea sulfate reduction is an
important component of the oceanic sulphur cycle as a whole. More specifically,
this terminal electron accepting pathway is of major importance for the
degradation of organic matter in the deep. As described in other blogs, deep-sea
wood falls are firstly colonised by heterotrophic bacteria who break down the
cellulose and provide substrates for fermentation reactions. From this point
sulfate reducing bacteria can use the produced H2 and create sulfidic
niches, which are postulated to attract higher chemosynthetic organisms and
their symbionts. Pradel et al. (2013) were interested in one specific sulfate
reducing bacteria, Desulfovibrio
piezophilus, a piezophilic (organism which thrives at high pressures) anaerobe
which was isolated from a wood fall in the Mediterranean. The authors used D.piezophilus as a model organism to
study the adaption of sulfate reducing bacteria to high hydrostatic pressure
habitats.
Pradel et al. (2013) present the first genomic and
proteomic characterisation of a deep-sea sulfate reducer. Briefly, the organism
has 3.6Mbp arranged in one circular molecule, a GC content of 50%, 7 genomic
islands and 3,424 coding DNA sequences (CDs). Comparing proteomic data at
different pressures allowed the detection of pressure related changes in protein
production which was speculated to be important points for pressure adaption.
Some key enzymes in sulfate reduction were indeed pressure dependant.
On its own this genome/proteome publication is
merely another species specific contribution to the literature. However it
clearly provides much needed in-depth detail on the structure of the genes and
proteins present which could be useful candidates for further work. With the
genome/proteome data, there is now opportunity to understand both the deep-sea
microbial contribution to the oceanic sulphur cycle and adaption strategies to
high pressure environments. Using the candidate genes and proteins identified
by this study, further work should include experimental methods to increase
understanding of function.
Pradel, N.,
Ji, B., Gimenez, G., Talla, E., Lenoble, P., Garel, M., Tamburini, C., et al.
(2013). The First Genomic
and Proteomic Characterization of a Deep-Sea Sulfate Reducer: Insights into the
Piezophilic Lifestyle of Desulfovibrio piezophilus. (V. de Crécy-Lagard, Ed.)PLoS
ONE, 8(1)
hey vicky, did the key enzymes prefer an increase in pressure? or was it the other way round as you've said the key enzymes were pressure dependent, is there a specific pressure they thrive at or a trend seen as you increase it so to speak.
ReplyDeletethanks
Ollie
Hi Ollie,
ReplyDeleteThanks for the comment :+) good question! Sorry I wasn’t clear about the pressure dependant part, I found it a bit tricky pulling out the key info on this paper as it was a whopping 11 pages of genomic and proteomic detail!
So basically they did some experimental work in which cultures were grown at different pressures, 0.1 and 10 Megapascals (MPa 1MPa = 10bar), they then classified the proteome of the cultures in different conditions to identify pressure-dependent variations in proteins. They found that some proteins increased at pressure whilst others decreased, they postulate these as areas for adaption to pressure.
I found it a bit strange hence I didn’t go into detail in the blog, when looking carefully at the table I noticed that some of the sulfate reduction proteins decreased under low pressure (Flavin protein QmoA) and others increased under low pressure (Periplasmic hydrogenase and Adenylyl sulfate reductase). I don’t know a lot about the specifics of the sulfate reduction pathway and therefore I can’t fully interpret the significance of this, but as far as I understand, the conclusion is that certain enzymes are adapted to pressure whilst others aren’t.
Hope that helps,
Best wishes,
Vicky
hey, thats fine you understood about the same as me haha, but yes thats fine thankyou very much. I'll try and rack my brain and figure it out.
ReplyDeleteThanks
Ollie.