Difference between revisions of "Karen's Assignment"

Revision as of 16:48, 29 September 2009

Potassium homeostasis

How does our species maintain potassium homeostasis?

In JGI's list of genes with predicted functions, I found the following 10 genes related to K+ (6 of which were called in RAST):
K+ transport system, NAD-binding component

2603205..2603861(+)

Trk system potassium uptake protein trkA-1

Start 2603205
Stop 2603861

This is the same as a JGI called gene.

K+ transport system, NAD-binding component

2199065..2199751(+)

Trk system potassium uptake protein trkA-3

Start 2199116
Stop 2199751

Similar to a JGI called gene, but the start position is later in RAST than JGI.

K+ transport system, NAD-binding component

2210390..2211088(-)

Kef-type K+ ransport system, predicted NAD-binding component

2271340..2272527(+)

Kef-type K+ transport system, membrane component

2954301..2955512(+)

K+ transport system, NAD-binding component

1938027..1939364(-)

Trk system potassium uptake protein trkA-4

Start 1939364
Stop 1938027

This is the same as a JGI called gene.

Trk-type K+ transport system, membrane component

1939429..1940991(-)

Potassium uptake protein TrkH

Start 1940991
Stop 1939429

This is the same as a JGI called gene.

K+ transport system, NAD-binding component

2797145..2798779(-)

Potassium channel protein-1

Start 2798779
Stop 2797145

This is the same as a JGI called gene.

K+ transport system, NAD-binding component

1146592..1148280(-)

NhaP-type Na+(K+)/H+ antiporter

3021102..3022994(+)

Trk system potassium uptake protein trkA-2

Start 3021102
Stop 3022994

This is the same as a JGI called gene.

I found no genes with predicted functions that are associated with Cl- from JGI

In RAST, I found seven genes related to potassium homeostasis that were not called in JGI:

Cobalt-zinc-cadmium resistance protein

Start: 2285691
Stop: 2284783

Phosphoribosylglycinamide formyltransferase (EC 2.1.2.2) / Phosphoribosylaminoimidazolecarboxamide formyltransferase (EC 2.1.2.3)

Start 678963
Stop 680573

Hydroxyacylglutathione hydrolase (EC 3.1.2.6)-1

Start 2604831
Stop 2605442

Hydroxyacylglutathione hydrolase (EC 3.1.2.6)-2

Start 1276452
Stop 1277027

Kef-type K+ transport systems (NAD-binding component fused to domain related to exopolyphosphatase)-1

Start 1431353
Stop 1429968

Kef-type K+ transport systems (NAD-binding component fused to domain related to exopolyphosphatase)-2

Start 1650228
Stop 1648756

Potassium channel protein-2

Start 2916660
Stop 2915455

I found no genes with predicted functions that are associated with Cl- function on RAST.

Are the genes for this process highly conserved among halophiles?

Blast results for JGI genes:

Blastn results for K+ transport system, NAD-binding component

Haloarcula marismortui ATCC 43049 chromosome I, complete sequence 




Halobacterium salinarum complete genome, strain R1 



Halobacterium sp. NRC-1, complete genome

Blastn results for K+ transport system, NAD-binding component

Haloarcula marismortui ATCC 43049 chromosome I, complete sequence



Halobacterium salinarum complete genome, strain R1


Halobacterium sp. NRC-1, complete genome

Blastn results for K+ transport system, NAD-binding component

Haloarcula marismortui ATCC 43049 chromosome I, complete sequence

Blastn results for Kef-type K+ ransport system, predicted NAD-binding component

Haloarcula marismortui ATCC 43049 chromosome I, complete sequence

 

Halorubrum lacusprofundi ATCC 49239 chromosome 1, complete sequence



Halobacterium salinarum complete genome, strain R1



Halobacterium sp. NRC-1, complete genome



Natronomonas pharaonis DSM 2160 complete genome

Blastn results for Kef-type K+ transport system, membrane component

Halorubrum lacusprofundi ATCC 49239 chromosome 1, complete sequence


Haloarcula marismortui ATCC 43049 chromosome I, complete sequence

Blastn results for K+ transport system, NAD-binding component

Halorubrum lacusprofundi ATCC 49239 chromosome 1, complete sequence


Natronomonas pharaonis DSM 2160 complete genome

Blastn results for Trk-type K+ transport system, membrane component

Natronomonas pharaonis DSM 2160 complete genome


[Halorubrum lacusprofundi ATCC 49239 chromosome 1, complete sequence http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=nucleotide&dopt=GenBank&RID=BJ9VZPHM01N&log%24=nuclalign&blast_rank=3&list_uids=222451341]


Haloarcula marismortui ATCC 43049 chromosome I, complete sequence


Halobacterium salinarum PHS3 plasmid complete genome, strain

Blastn results for K+ transport system, NAD-binding component

Haloarcula marismortui ATCC 43049 chromosome I, complete sequence


Halobacterium salinarum complete genome, strain R1


Halobacterium sp. NRC-1, complete genome


Halorubrum lacusprofundi ATCC 49239 chromosome 1, complete sequence

The blastn results are becoming very repetitive. I think at this point, the way to attack this problem may be to look into this list of 5-6 species that seem to share the potassium proteins seen in our species. If I can find a common thread in how other species are utilizing the same potassium homeostasis machinery, it will tell me a great deal about how our own species is using all these potassium related genes.

It is important to note that many of these genes were also related to the species Halorhabdus utahensis. I did not include the blastn results for this species because Blast could not specify which gene segment these matches were a part of. I believe this was not included simply because this species has not been annotated (or the annotation has not been entered into blast). In any comparison of species that takes place after this, I will need to include this species as well.

Is potassium homeostasis related to our species ability to survive/thrive in high salinity environments? How?

"Cell membranes are freely permeable to water, so the only way to prevent the loss of cellular water under high salt conditions is to increase the internal solute concentration. Halotolerantand halophilic microorganisms therefore accumulate high solute concentrations within the cytoplasm." [1]

I am beginning to understand potassium homeostasis and how it may be useful to our organism to survive in high salt concentrations by first researching how other known species utilize this mechanism. In a paper by Strahl and Greie, the Halobacterium salinarum species use of potassium homeostasis to maintain life in a high salinity environment is described. Apparently these organisms maintain life in such conditions by creating an equimolar condition within their cytoplasm. KCl is the preferred ion to create this equal osmolality for this halobacterium resulting in osmotic equilibrium with the surrounding environment. The K+ ion enters the cell by both passive transport mechanisms as well as active transport mechanisms. A gene, kdpFABC, has been discovered in this organism that codes for homologs of a bacterial ATP-driven K+ uptake system. Deletion of this gene is detrimental to organism survival in limiting K+ conditions. This paper also mentions that this mechanism is unique to this and another species of halobacterium because other halophiles utilize organic solutes to equalize osmotic pressures in high salinity environments. I must determine whether or not potassium homeostasis could be a mechanism of maintaining osmotic equilibrium in our species.

A paper by Oren et al. describes another species, Salinibacter ruber, that appears to be capable of surviving in high salinity environments due to the uptake of high concentrations of potassium. The finding that potassium homeostasis seems to be the mechanism of maintaining life in a high salinity environment was determined by measuring K+, Cl+, glutamate, glycine betaine, and N-alpha-acetyllysine concentrations within the cytoplasm. High amounts of K+ and Cl+ were found within the cytoplasm but low amounts of glutamate, glycine betaine, and N-alpha-acetyllysine were discovered. These three organic solutes are often associated with maintaining osmotic equilibrium in archaic halophiles that exist in high salinity environments. It is unusual that this species does not utilize these organic solutes to maintain homeostasis but instead seems to be utilizing the inorganic molecule KCl. This paper provides another example of potassium concentrations being utilized to maintain life in high salinity environments. I need to determine if our species is using this inorganic molecule or the more common organic molecules to maintain osmotic balance in a high salinity environment.

H. salinarum K+ transport mechanism comparison Found the nucleotide sequence for the KdpFABC operon in the species H. salinarum using NCBI. Compared this sequence to our species genome using Blastx. Found three significant hits:

heavy metal translocating P-type ATPase-1

heavy metal translocating P-type ATPase-2

heavy metal translocating P-type ATPase-3

These hits could just be related to the ATPase function of the Kdp operon in H. salinarum and have nothing to do with potassium transport. I am going to redo this blastx with individual genes from operon Kdp compared to our species genome separately. When blasted separately, I found that the three hits from above were in the gene KdpB in the operon of H salinarum. No other similarities, however, were discovered.