Nirtogen is a key element in the oceans. Atmospheric
nitrogen must be converted into ammonium before it can be used. This is called
biological nitrogen fixation (BNF). BNF is carried out by a small group of
microorganisms called diazotrophs. Little is known about this group and they
were identified using polymerase chain reaction amplification of the nifH gene which encodes the enzyme nitrogenase.
Nitrogenase enzymes have been shown to require iron by previous studies and it
is believed that the availability of iron and phosphorous may be important
limiting or co-limiting factors in BNF.
This study by Turk et
al (2011) focused on BNF and nifH
expression near the Cape Verde islands in the eastern North Atlantic; it is a
unique study because it is the first to look at nifH expression in these waters. This region generally has depleted
nutrient levels but is heavily influenced by Saharan dusts which may supply
iron and phosphorus to the area.
Samples were collected from 6 stations chosen to give a
gradient from near shore to open waters. Nitrogen fixation rates, background nitrogen
levels, total dissolved iron and nitrogen levels were measured at all 6
stations to be used later. The study
aimed to do three main things firstly describe the diversity of nifH-containing organisms actively
transcribing nitrogenise by Reverse-transcription PCR(RT-PCR), secondly
quantifying the nifH transcripts from 7 major cyanobacteria by quantitative RT-PCR and
thirdly measuring BNF.
The results of this study showed a positive correlation between
BNF rates and dissolved iron levels but it was not show to correlate with
phosphorus. This provides evidence for the link between BNF and Saharan dust. A
total of 605 nifH transcripts were isolated
from the samples of which 76% were from 6 operational taxonomic units including
Trichodesmonium, uncultivated UCYN-A
and 4 non-cyanobacterial diazotrophs.
UCYN-A (a type of cyanobacteria) was
found to contribute most significantly to the pool of nifH in coastal and oligitrophic waters which indicates that they
may be important contributors to BNF in this region. This contrasts with other
studies carried out in the eastern equatorial Atlantic where nifH expression is dominated by Trichodesmium.
The authors of this paper recognise that the their methods
have some limitations for example the PCR method means that only certain thing
are targeted by the qPCR assays therefore other non targeted phylotypes may
contribute to the pool of nifH
transcripts. The methods used to measure nitrogen fixation rates have also
recently been brought into question as this method may underestimate fixation rates.
Overall I found this paper quite difficult to interpret
because of the way it was written which made it hard to follow. I chose to review this paper because it linked with our lectures
on the nitrogen cycle.
Kendra A Turk, Andrew
P Rees, Jonathan P Zehr, Nicole Pereira,
Paul Swift, Rachel Shelley, Maeve Lohan,
E Malcolm S Woodward and
Jack Gilbert (2011) The ISME Journal (2011) 5, 1201–1212; doi:10.1038/ismej.2010.205
Here is a link to the original paper:
http://www.nature.com/ismej/journal/v5/n7/full/ismej2010205a.html
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