Haloarcula Marismortui: Difference between revisions

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==Genome structure==
==Genome structure==
H. marismortui has a genome that is 4275kb in size composed of nine replicons and 4242 protein coding genes. It is divided into high and low G+C content replicons. The large chromosome I is a 3132-kb replicon with a 62.36% G+C content. The other eight replicons are smaller, ranging from 33 to 410 kb with G+C contents ranging from 54.25% to 60.02%, averaging about 57%. This bipartite genome-content organization is generally found in all members of this group of organisms. The significance of this type of organization is unknown.  
H. marismortui has a genome that is 4275kb in size composed of nine replicons and 4242 protein coding genes. It is divided into high and low G+C content replicons. The large chromosome I is a 3132-kb replicon with a 62.36% G+C content. The other eight replicons are smaller, ranging from 33 to 410 kb with G+C contents ranging from 54.25% to 60.02%, averaging about 57%. This bipartite genome-content organization is generally found in all members of this group of organisms. The significance of this type of organization is unknown.  
However, there are three small replicons in H. marismortui that encode functions that are essential for survival. Replicon pNG600 codes several genes that are found nowhere else in the genome of H. marismortuis: aconitase, a significant enzyme in the TCA cycle, a DNA polymerase B family protein, the large and small subunits of endonuclease VII, and two transcription factor B (TFB) orthologs. This replicon is also responsible for H. marismortuis’s ability to handle heavy metal stress. It encodes genes for about a dozen cation transport proteins that have various specificities, metal-ion dependent transcription regulators, and a mercuric reductase.
 
Replicon pNG700 codes for four essential enzymes used in folate metabolism: viz. methylenetetrahydrofolate dehydrogenase, 5, 10-methylentretrahydrofolate reductase, formyltetrahydrofolate synthetase and formimidoyltetrahydrofolate cyclodeaminase. It also codes for functions that act downstream to arginine breakdown.
However, there are three small replicons in H. marismortui that encode functions that are essential for survival. Replicon pNG600 codes several genes that are found nowhere else in the genome of H. marismortuis: aconitase, a significant enzyme in the TCA cycle, a DNA polymerase B family protein, the large and small subunits of endonuclease VII, and two transcription factor B (TFB) orthologs. This replicon is also responsible for H. marismortuis’s ability to handle heavy metal stress. It encodes genes for about a dozen cation transport proteins that have various specificities, metal-ion dependent transcription regulators, and a mercuric reductase.
Chromosome II is the third replicon that encodes essential functions. It encodes one of three rRNA operons, as well as carbamoyl phosphate synthase, succinate-semialdehyde dehydrogenase, pyruvate dehydrogenase, acetyl-CoA acetyltransferase, citrate lyase, and GMP synthase, which are all foundational in essential metabolic processes. (2)
 
Replicon pNG700 codes for four essential enzymes used in folate metabolism: viz. methylenetetrahydrofolate dehydrogenase, 5, 10-methylentretrahydrofolate reductase, formyltetrahydrofolate synthetase and formimidoyltetrahydrofolate cyclodeaminase. It also codes for functions that act downstream to arginine breakdown.
 
Chromosome II is the third replicon that encodes essential functions. It encodes one of three rRNA operons, as well as carbamoyl phosphate synthase, succinate-semialdehyde dehydrogenase, pyruvate dehydrogenase, acetyl-CoA acetyltransferase, citrate lyase, and GMP synthase, which are all foundational in essential metabolic processes. (2)


==Cell structure and metabolism==
==Cell structure and metabolism==

Revision as of 06:55, 5 June 2007

A Microbial Biorealm page on the genus Haloarcula Marismortui

Classification (1)

Higher order taxa

Cellular organisms; Archaea; Euryarchaeota; Halobacteria; Halobacteriales; Halobacteriaceae; Haloarcula

Species

NCBI: Taxonomy

Haloarcula marismortui

Description and significance

Haloarcula marismortui is a halophilic red Archaeon (from the Halobacteriaceae family) found in the Dead Sea, a high saline, low oxygen solubility, and high light intensity environment. Like other halophilic archaeal organisms, H. marismortui thrives in this extreme environment due to several adaptations in protein structure, metabolic strategies and physiologic responses. (2, 3)

It is important to have its genome sequenced because of its unique ability to survive in such an extreme environment. The three fold extremities listed above are not expected characteristics of an environment in which a particular organism is able to survive. Therefore, it is important to understand what physiologic responses are unique to the organism that allows it to thrive in such an extreme environment. This will allow researchers to understand the systems level mechanisms that underlie environmental response systems. Analyzing its genome also provides support for the previously proposed characteristics of halophilic archaea, like acidic proteome, as well as the evolution of their genome architecture. A better understanding of gene regulatory networks that influence protein-protein and protein-DNA interactions may also provide a framework for biotechnological applications in the future. See Application section below for a more detailed description. (2, 3)

It was isolated in the 1960s by Ginzburg et al. in the Dead Sea. It is very closely related to Haloarcula vallismortis, but differs in its cell morphology and ability to use different sugars and other compounds for function. (4)

Genome structure

H. marismortui has a genome that is 4275kb in size composed of nine replicons and 4242 protein coding genes. It is divided into high and low G+C content replicons. The large chromosome I is a 3132-kb replicon with a 62.36% G+C content. The other eight replicons are smaller, ranging from 33 to 410 kb with G+C contents ranging from 54.25% to 60.02%, averaging about 57%. This bipartite genome-content organization is generally found in all members of this group of organisms. The significance of this type of organization is unknown.

However, there are three small replicons in H. marismortui that encode functions that are essential for survival. Replicon pNG600 codes several genes that are found nowhere else in the genome of H. marismortuis: aconitase, a significant enzyme in the TCA cycle, a DNA polymerase B family protein, the large and small subunits of endonuclease VII, and two transcription factor B (TFB) orthologs. This replicon is also responsible for H. marismortuis’s ability to handle heavy metal stress. It encodes genes for about a dozen cation transport proteins that have various specificities, metal-ion dependent transcription regulators, and a mercuric reductase.

Replicon pNG700 codes for four essential enzymes used in folate metabolism: viz. methylenetetrahydrofolate dehydrogenase, 5, 10-methylentretrahydrofolate reductase, formyltetrahydrofolate synthetase and formimidoyltetrahydrofolate cyclodeaminase. It also codes for functions that act downstream to arginine breakdown.

Chromosome II is the third replicon that encodes essential functions. It encodes one of three rRNA operons, as well as carbamoyl phosphate synthase, succinate-semialdehyde dehydrogenase, pyruvate dehydrogenase, acetyl-CoA acetyltransferase, citrate lyase, and GMP synthase, which are all foundational in essential metabolic processes. (2)

Cell structure and metabolism

Describe any interesting features and/or cell structures; how it gains energy; what important molecules it produces.

Ecology

Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.

Pathology

How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.

Application to Biotechnology

Does this organism produce any useful compounds or enzymes? What are they and how are they used?

Current Research

Enter summaries of the most recent research here--at least three required

References

[Sample reference] Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "Palaeococcus ferrophilus gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". International Journal of Systematic and Evolutionary Microbiology. 2000. Volume 50. p. 489-500.

Edited by student of Rachel Larsen and Kit Pogliano