Mycobacterium vanbaalenii: Difference between revisions

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==Application to Biotechnology==
==Application to Biotechnology==
<i>M. vanbaalenii</i> is an ideal candidate for bioremediation in contaminated areas of the environment. First discovered in 1986 on contaminated sites it was the first known micro-organism to be able to degrade polycyclic aromatic hydrocarbons of more than three aromatic rings. Studies are being conducted on how <i>M. vanbaalenii</i> may prove useful in the degradation of larger PAH molecules such as benzo[a]pyrene. Although there are no definite results on its effect to humans the Environmental Protection Agency (EPA) has shown BaP to be carcinogenic to various mammals including some primates. Exposure to drinking water contaminated to BaP resulted in tumors in various locations such as the forestomach and esophagus. As well as its proven carcinogenic effects BaP has also been shown to be genotoxic to various prokaryotic and mammalian DNA. (Reference EPA) A terminal deoxygenase has been found to be an important factor in PAH degradation in <i>M. vanbaalenii’s</i> pathway to transform BaP into various metabolites. In studies, results showed that <i>M. vanbaalenii</i> was able to convert BaP into benzo[a]pyrene cis-4R,5S-dihydrodiol and benzo[a]pyrene cis-4S,5R-dihydrodiol both non-toxic and non-carcinogenic. It’s regioselectivity in degrading compounds and forming others may also be studied for other pharmaceutical or industrial purposes. (Reference Reading 1)
<i>M. vanbaalenii</i> is an ideal candidate for bioremediation in contaminated areas of the environment. First discovered in 1986 on contaminated sites it was the first known micro-organism to be able to degrade polycyclic aromatic hydrocarbons of more than three aromatic rings. [4] Studies are being conducted on how <i>M. vanbaalenii</i> may prove useful in the degradation of larger PAH molecules such as benzo[a]pyrene. Although there are no definite results on its effect to humans the Environmental Protection Agency (EPA) has shown BaP to be carcinogenic to various mammals including some primates. Exposure to drinking water contaminated to BaP resulted in tumors in various locations such as the forestomach and esophagus. As well as its proven carcinogenic effects BaP has also been shown to be genotoxic to various prokaryotic and mammalian DNA. [9] A terminal deoxygenase has been found to be an important factor in PAH degradation in <i>M. vanbaalenii’s</i> pathway to transform BaP into various metabolites. In studies, results showed that <i>M. vanbaalenii</i> was able to convert BaP into benzo[a]pyrene cis-4R,5S-dihydrodiol and benzo[a]pyrene cis-4S,5R-dihydrodiol both non-toxic and non-carcinogenic. It’s regioselectivity in degrading compounds and forming others may also be studied for other pharmaceutical or industrial purposes. [5]


==Current Research==
==Current Research==

Revision as of 02:24, 5 June 2007

Mycobacterium vanbaalenii

(This page is currently under construction)

A Microbial Biorealm page on the genus Mycobacterium vanbaalenii

Classification

Higher order taxa

Bacteria; Actinobacteria; Actinobacteridae; Actinomycetales; Coyrnebacterineae; Mycobacteriaceae; Mycobacterium; Mycobacterium vanbaalenii PYR-1

Genus

Mycobacterium vanbaalenii


NCBI: Taxonomy


Description

Some members of the Mycobacterium genus are able to degrade various environmentally toxic chemicals. Mycobacterium vanbaalenii PYR-1 was first found in the Harbor Island oil tank farm in the watershed of Redfish Bay, Texas in 1986. It is notable for it’s ability to degrade polycyclic aromatic hydrocarbons (PAHs) such as pyrene as its sole carbon and energy source. PAH are common organic pollutants; some, i.e. pyrene, is found in incompletely combusted petroleum products. Some PAHs have been identified as carcinogens and pyrene itself is known to be toxic to the liver and kidneys. It has been proposed that the understanding of the genome sequence of the PYR-1 strain will allow an understanding of the PAH degradation pathway and may prove useful ecologically in bioremediation processes. [2]

Cultures of M. vanbaalenii grow in colonies of 0.5 - 1.0nm. The colonies are circular, smooth and convex with the surface of the plate. Individual cells are shaped typical of the Mycobacteria genus, slim and rod-shaped. They are 0.7 - 1.4μm in length and 0.4 - 0.7μm in width. [4]

Genome structure

The PYR-1 strain has a circular chromosome. It has 5,979 protein genes, and 58 RNA genes. It has 6,491,865 base pairs with a G+C content of 67.8%, 91% of these genes code for something (are functional). It contains 99 pseudogenes. These are genes which accumulate mutations at a higher rate, rendering them non-functional. [1]

Stothard P, Van Domselaar G, Shrivastava S, Guo A, O'Neill B, Cruz J, Ellison M, Wishart DS (2005)

Two genes nidA and nidB have been identified as the genes which code for the large and small subunits of a PAH dioxygenase. The dioxygenase is an enzyme that catalyzes both oxygen atoms in O_2 into a single substrate and has been shown to be involved in the PAH degradation pathway of M. vanbaalenii. The proteins of these genes are conserved homologues to other proteins in other soil Mycobacterium species which indicate they may be important in PAH degradation.

An operon for the regulatory protein phtR and five genes closely located to each other; phtAa, phtAb, phtB, phtAc, and phtAd have been found close to the nidA and nidB genes. These genes are important for the degradation of phthalate, an intermediate in the degradation of three known PAH’s in M. vanbaalenii, and is currently be studied.

Further understanding of these genes and the enzymes they code may prove useful in the current studies of M. vanbaalenii and its relatives and their degradative properties of the harmful PAH compounds. [7]

Cell structure and metabolism

Mycobacteria are in the group of Actinobacteria, Gram-positive bacteria who live mostly in the soil and are involved in the degradation of organic materials. Like other Mycobacterium, M. vanbaalenii is an acid-fast, aerobic bacteria which stains Gram-positive which means it has only one inner cell membrane and a thick cell wall (unlike cells who stain Gram-negative which have two cell membranes and a thin cell wall in between). It is a rod-shaped, non-motile, and non-sporulating organism. Cells can grow singly, paired, or clustered with almost no pleomorphism, or variation in cell size and nucleus shape. It has only one layer of cell wall, which is hydrophobic, waxy, and thicker than the cell walls of most other bacteria. Mycolic acid makes up much of this cell wall and gives the genus (Mycobacterium) its name. [3]

It has been deduced that the majority of M. vanbaalenii’s energy is derived from the metabolic degradation of PAHs for carbon and energy source. Due to its thick, waxy cell wall this genus of bacteria are very hardy. M. vanbaalenii's metabolic rates peak when it is in an environment of 24-30°C, suggesting that this is the optimal temperature for growth. There was no observable growth at 5°C or 42°C. [4]

Ecology

Most Mycobacteria, excepting a few obligate, pathogenic bacteria, are found in the soil. M. vanbaalenii in particular is often found in contaminated soils or wells and plays an important role degrading toxic pollutants in the soil. There are at least 16 polycyclic aromatic hydrocarbons (PAHs) listed by the U.S. Environmental Protection Agency as priority pollutants due to toxicity and ubiquity. [4] PAH's are components of products such as crude oil used by humans and may enter into the environment through means such as combustion of fossil fuels. While PAH’s of low molecular density have been shown to degrade naturally, PAH’s of higher molecular density (molecules of four rings and more) are much harder to degrade and may persist in the environment. Different PAH’s have different effects, however, there have been proven toxic, mutagenic, and in some cases carcinogenic effects of some PAH’s which makes it important to find methods to degrade these compounds. M. vanbaalenii has already proven to be effective in degrading four-ring compounds such as pyrene, readily mineralizing pyrene into carbon dioxide. This is an important step towards bioremediation of polluted environmental sites. [5] M. vanbaalenii are one of the micro-organisms being studied now in the hopes of reducing the effects that these compounds have on (more immediately) aquatic animals and, potentially, humans. [4]

Pathology

M. vanbaalenii comes from a diverse genus of bacteria. On the whole, most Mycobacteria are non-pathogenic soil bacteria and survive on their own. A few species, however, such as M. tuberculosis and M. leprae are obligate parasites and need hosts to survive. The mycolic acid layer that the single waxy layer of the cell wall characteristic in all the species in the Mycobacterium genus also contributes to the slow growth rate as well as the hardiness of the pathogenic strains such as M. tuberculosis, a pathogen which targets only humans. This makes the pathogenic strains very resistant to antibiotics.

M. vanbaalenii is non-pathogenic and is currently characterized under risk group 1. Like other Mycobacteria which uses the degradation of various compounds found in the soil (PAH for M. vanbaalenii) it is currently being studied for its potential to reduce environmental pollution, not its risk to the health of humans or animals.

Application to Biotechnology

M. vanbaalenii is an ideal candidate for bioremediation in contaminated areas of the environment. First discovered in 1986 on contaminated sites it was the first known micro-organism to be able to degrade polycyclic aromatic hydrocarbons of more than three aromatic rings. [4] Studies are being conducted on how M. vanbaalenii may prove useful in the degradation of larger PAH molecules such as benzo[a]pyrene. Although there are no definite results on its effect to humans the Environmental Protection Agency (EPA) has shown BaP to be carcinogenic to various mammals including some primates. Exposure to drinking water contaminated to BaP resulted in tumors in various locations such as the forestomach and esophagus. As well as its proven carcinogenic effects BaP has also been shown to be genotoxic to various prokaryotic and mammalian DNA. [9] A terminal deoxygenase has been found to be an important factor in PAH degradation in M. vanbaalenii’s pathway to transform BaP into various metabolites. In studies, results showed that M. vanbaalenii was able to convert BaP into benzo[a]pyrene cis-4R,5S-dihydrodiol and benzo[a]pyrene cis-4S,5R-dihydrodiol both non-toxic and non-carcinogenic. It’s regioselectivity in degrading compounds and forming others may also be studied for other pharmaceutical or industrial purposes. [5]

Current Research

1. This paper (referenced below) studies the degradation of three particular polycyclic aromatic hydrocarbons, pyrene (PYR), benz[a]anthracene (BAA), and benzo[a]pyrene (BaP) by M. vanbaalenii. The studies focus on the degradative processes and identifies three metabolites formed in the study with PYR. Different cleavage products were identified for BAA, and BaP and explores the possibility that the bacterium may be capable of attacking and degrading BAA and BaP from different sites of the compounds. These reactions are believed to occur through dioxygenase enzymatic processes.

2. This article studies the metabolic pathway of benzo[a]pyrene degradation by M. vanbaalenii PYR-1. More specifically it studies the reactions, the stereo and regio-selectivity of the enzymes (oxygenases) that act in this pathway. The metabolites are separated and identified and the previously reported metabolic pathway is extended with the new evidence presented in this article.

3. This article states that the study identified an operon within the M. vanbaalenii PYR-1 genome for putative phthalate dioxygenase. Phthalates are compounds commonly used as plasticizers which have been known to cause carcinogens in lab studies. This study is the first on a phthalate degradation operon in the M. vanbaalenii and includes brief notes on how it differs from those in other Gram-positive bacteria in terms of gene location and orientation.

4. This article uses various methods to study and complete the metabolic path that M. vanbaalenii takes in the degradation of pyrene. In this study 1028 proteins and 27 enzymes are identified for the complete degradative process which is presented among the results. This study hopes to further elucidate the process involved in PAH degradation, especially that of high-molecular weight PAHs.

References

References

1. http://www.genome.jp/kegg-bin/show_organism?menu_type=genome_info&org=mva

2. http://genome.jgi-psf.org/finished_microbes/mycva/mycva.home.html

3. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genomeprj&cmd=Retrieve&dopt=Overview&list_uids=15761

4. Heitkamp, M. A., Franklin, W., Cerniglia, C. E. Microbial metabolism of polycyclic aromatic hydrocarbons: isolation and characterization of a pyrene-degrading bacterium. http://aem.asm.org/cgi/reprint/54/10/2549?view=long&pmid=3202633

5. Roten C.-A.H. Gamba P. Barblan J.-L. Karamata D. Comparative Genometrics (CG): a database dedicated to biometric comparisons of whole genomes. Nucleic Acids Res 2002 Jan 1;30(1):142-4 http://www2.unil.ch/comparativegenometrics/References.html

6. http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=2261&lvl=3&keep=1&srchmode=1&unlock&lin=f

Current Research

1. Joanne Schneider, Robert Grosser, Koka Jay Asimhulu, Weiling Xue, and David Warshawsky. Degradation of Pyrene, Benz[a]anthracene, and Benz[a]pyrene by Mycobacterium sp. Strain RJGII-135, Isolated from a Former Coal Gasification Site. 1995 http://aem.asm.org/cgi/reprint/62/1/13?view=long&pmid=8572690

2. Joanna D. Moody,1 James P. Freeman,2 Peter P. Fu,3 and Carl E. Cerniglia1 Degradation of Benzo[a]pyrene by Mycobacterium vanbaalenii PYR-1. Received July 28, 2003; Accepted October 6, 2003. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=321301

3. Robin L. Stingley1, Barbara Brezna1,2, Ashraf A. Khan1 and Carl E. Cerniglia. Novel organization of genes in a phthalate degradation operon of Mycobacterium vanbaalenii PYR-1. http://mic.sgmjournals.org/cgi/content/abstract/150/11/3749

4. Seong-Jae Kim, Ohgew Kweon, Richard C. Jones, James P. Freeman, Ricky D. Edmondson, and Carl E. Cerniglia. Complete and Integrated Pyrene Degradation Pathway in Mycobacterium vanbaalenii PYR-1 Based on Systems Biology. 2006 http://jb.asm.org/cgi/reprint/189/2/464


Edited by M.Chu, student of Rachel Larsen and Kit Pogliano