Rickettsia prowazekii: Difference between revisions
| Line 29: | Line 29: | ||
==Cell structure and metabolism== | ==Cell structure and metabolism== | ||
''R. prowazekii'' is a Gram-, intracellular bacteria with a bacilli (rod like) structure. Genomic codes for LPS and Peptidoglycan formation are both complete in ''R. prowazekii'. | ''R. prowazekii'' is a Gram-, intracellular bacteria with a bacilli (rod like) structure. Genomic codes for LPS and Peptidoglycan formation are both complete in ''R. prowazekii'. | ||
As mentioned above, ''R. prowazekii'' cannot produce pyruvate from any glycolytic pathway. However, enzymes required for pyruvate metabolism are coded for by ''Rickettsia'' indicating that the microbe must acquire it somehow. One such mechanism for this acquisition is acquiring Phosphoenol Pyruvate (PEP) directly from it's host. ''Rickettsia'' also lack coding sequences for Nitrogen metabolism which allows the synthesis of glutamine, indicating that, like PEP, glutamine must be acquired directly from the host cells. | As mentioned above, ''R. prowazekii'' cannot produce pyruvate from any glycolytic pathway. However, enzymes required for pyruvate metabolism are coded for by ''Rickettsia'' indicating that the microbe must acquire it somehow. One such mechanism for this acquisition is acquiring Phosphoenol Pyruvate (PEP) directly from it's host. ''Rickettsia'' also lack coding sequences for Nitrogen metabolism which allows the synthesis of glutamine, indicating that, like PEP, glutamine must be acquired directly from the host cells. [2] | ||
''Rickettsia'' also gain energy from oxidative phosphorylation and ATP translocases. First, ''Rickettsia'' code for 5 copies of ATP translocases indicating the importance they have in obtaining energy for the microbe. The translocases allow the cell to take up ATP produced by the host. This is the major ATP capturing method for ''Rickettsia'' since the cell will use translocases after entering a host cell to capture the host ATP before initiating its own pathways. Once it has used up all the host ATP, it will initiate the electron transport chain, which culminates with ATP Synthase and the production of ATP. | ''Rickettsia'' also gain energy from oxidative phosphorylation and ATP translocases. First, ''Rickettsia'' code for 5 copies of ATP translocases indicating the importance they have in obtaining energy for the microbe. The translocases allow the cell to take up ATP produced by the host. This is the major ATP capturing method for ''Rickettsia'' since the cell will use translocases after entering a host cell to capture the host ATP before initiating its own pathways. Once it has used up all the host ATP, it will initiate the electron transport chain, which culminates with ATP Synthase and the production of ATP. [2] | ||
Another key molecule produced is polyhydroxyalkanoate (PHA), | Another key molecule produced is polyhydroxyalkanoate (PHA), which is produced in high numbers when the nutrient source for the cell begins to diminsh. PHA's are great carbon storing molecules and in the case of cellular starvation, PHA will serve as a carbon and energy source to maintain survival. [5] | ||
==Ecology== | ==Ecology== | ||
Revision as of 14:45, 4 June 2007
A Microbial Biorealm page on the genus Rickettsia prowazekii
Classification
Higher order taxa
Bacteria; Proteobacteria; Alphaproteobacteria; Rickettsiales; Rickettsiaceae
Species
|
NCBI: Taxonomy |
Rickettsia prowazekii
Description and significance
Describe the appearance, habitat, etc. of the organism, and why it is important enough to have its genome sequenced. Describe how and where it was isolated. Include a picture or two (with sources) if you can find them.
Rickettsia prowazekii is an intracellular, bacilli bacteria that is the cause of epidemic typhus in humans. In the early 20th century, Howard Ricketts linked typhus to Spotted Fever while Stanislaus von Prowazek discovered typhus was transmitted to humans by the feces of lice, not the bite. Both Ricketts and Prowazek were killed by typhus while working with the disease, so the bacteria was named for them. The genome was fully sequenced by the end of the century. Since World War II the only other major breakout was during the Burundo civil war in the late 1990's. Now, the main point of research regarding R. prowazekii is its linkage to the origin of mitochondria. R. prowazekii has a small genome and is the first alpha-proteobacterial, gram negative genome to be sequenced.
Genome structure
Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence? Does it have any plasmids? Are they important to the organism's lifestyle?
The R. prowazekii genome is composed of a singular circular chromosome, containing 1,111,523 base pairs and 834 protein coding genes. Also, 24% of R. prowazekii DNA is non-coding- the largest amount in any microbial genome. No genes code for anaerobic glycolosis, however, complete coding sequences for the tricarboxylicacid (TCA) cycle and respiratory-chain complex are found.
Cell structure and metabolism
R. prowazekii is a Gram-, intracellular bacteria with a bacilli (rod like) structure. Genomic codes for LPS and Peptidoglycan formation are both complete in R. prowazekii'.
As mentioned above, R. prowazekii cannot produce pyruvate from any glycolytic pathway. However, enzymes required for pyruvate metabolism are coded for by Rickettsia indicating that the microbe must acquire it somehow. One such mechanism for this acquisition is acquiring Phosphoenol Pyruvate (PEP) directly from it's host. Rickettsia also lack coding sequences for Nitrogen metabolism which allows the synthesis of glutamine, indicating that, like PEP, glutamine must be acquired directly from the host cells. [2]
Rickettsia also gain energy from oxidative phosphorylation and ATP translocases. First, Rickettsia code for 5 copies of ATP translocases indicating the importance they have in obtaining energy for the microbe. The translocases allow the cell to take up ATP produced by the host. This is the major ATP capturing method for Rickettsia since the cell will use translocases after entering a host cell to capture the host ATP before initiating its own pathways. Once it has used up all the host ATP, it will initiate the electron transport chain, which culminates with ATP Synthase and the production of ATP. [2]
Another key molecule produced is polyhydroxyalkanoate (PHA), which is produced in high numbers when the nutrient source for the cell begins to diminsh. PHA's are great carbon storing molecules and in the case of cellular starvation, PHA will serve as a carbon and energy source to maintain survival. [5]
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?
As mentioned above in the Metabolism section, R. prowazekii produce PHA's which are excellent for storing carbon. Current reasearch on PHA's includes looking into their usefulness as a biodegradable plastic. PHA's exhibit material properties that can range from rubber-like to the stiff and brittle class of PHA's known as PHB (poly-beta-hydroxybutyrate) making them a very viable substitute for synthetic plastics. [5]
Current Research
Enter summaries of the most recent research here--at least three required
References
1 PATRIC: PathoSystems Resource Integration Center: Rickettsia prowazekii str. Madrid E
2 Some lessons from Rickettsia genomics FEMS Microbiol Rev. 2005 Jan;29(1):99-117
3 A century of typhus, lice and Rickettsia
5 Production of Polyhydroxyalkanoates, a bacterial biodegradable polymer
Edited by Matthew Noble, student of Rachel Larsen
