Photobacterium profundum

Taxobox
color = lightgrey
name = Photobacterium profundum

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image_caption = Confocal image of P. profundum Strain SS9 expressing a green fluorescent protein. Bar: 10μm
regnum = Bacteria
phylum = Proteobacteria
classis = Gammaproteobacteria
ordo = Vibrionales
familia = Vibrionaceae
genus = "Photobacterium"
species = "P. profundum"
binomial = "Photobacterium profundum""Photobacterium profundum" is a deep sea "Gammaproteobacterium", belonging to the family "Vibrionaceae" and genus "Photobacterium". Like other members of this genus, "P. profundum" is a marine organism and has two circular chromosomes [1] . "P. profundum" is a gram-negative rod with the ability for growth at temperatures from 0 °C to 25 °C and pressures from 0.1 MPa to 70 MPa depending on the strain. It has a requirement for salt, is able to metabolise a wide range of simple and complex carbohydrates and has two flagella systems. Cells are rod shape, 2-4μm long and 0.8-1.0μm wide, with a single unsheathed flagella [2] . This bacterium was originally isolated in 1986 from the Sulu Sea [3] and there are currently 4 cultured wild-type strains of "P. profundum", (strains SS9, 3TCK, DJS4 and 1230).

"P. profundum" strain SS9 has optimal growth at 15 °C and 28 MPa making it both a psychrophile and a piezophile. "P. profundum" strain 3TCK, isolates from San Diego Bay [4] , grows optimally at 9 °C and 0.1 MPa and "P. profundum" strain DSJ4, isolated from the Ryukya trench off of Japan at a depth of 5110 m, grows optimally at 10 °C and 10 MPa [2] . Based on 16S rRNA sequence "P. profundum" is closely related to the "Vibrio" genus, the most prominent species being the human pathogen "Vibrio cholerae".

In strain SS9 it has been shown that several stress response genes are up regulated in response to atmospheric pressure, these include htpG, dnaK, dnaJ, and groEL [1] . The types and abundance of fatty acid chains in the cell membrane also respond to changes in pressure and temperature [5] . At low temperature and high pressure strain SS9 increases the abundance of mono- and polyunsaturated fatty acids. This has the effect of increasing membrane fluidity by reducing packing of the fatty acid chains which results in a liquid crystal structure in the membrane rather than a gel structure [5] . The outer membrane protein OmpH has been shown to be up regulated at elevated pressures, the opposite is true for the outer membrane protein OmpL which is up regulated in response to low pressures [6] .

In 2005 Vezzi et al published the genome sequence for "P. profundum" strain SS9. The genome of "P. profundum" consists of a 4.1-Mbp circular chromosome, a 2.2-Mbp minor circular chromosome, as well as a 80-kbp circular plasmid. Strain SS9 has 14 ribosomal RNA (rRNA) genes on chromosome 1, and 1 on chromosome 2; this is the largest number of rRNA genes found in any bacterium. Chromosome 1 consists largely of genes which are essential for growth where as chromosome 2 appears to be a large plasmid, which, on an evolutionary time scale, has be gained several transposable elements [4] . With in the genome of "P. profundum" there is a large number of open reading frames (ORF) which are unique to SS9 and not found in other members of the "Vibrionaceae" family.

The genome sequence also highlighted a full Stickland pathway for the fermentation of amino acids; this was the first time this pathway has been identified in an aerobic bacterium. Two complete F1F0 ATP synthase pathways (one on each Chromosome) are also present in this bacterium: this might explain its ability to produce ATP at both high and low pressure.

This work was followed by another paper in 2005 by Campanaro et al [4] which detailed microarray work comparing gene expression at sub-optimal, optimal and supra-optimal temperatures and pressure for strains SS9, 3TCK and DSJ4. Campanaro et al showed that there are 544 ORF’s divergent or missing from the 3TCK genome and 562 ORF’s divergent or missing from the DSJ4 chromosomes when compared to that of SS9. This paper also highlighted that 3TCK lacks the lateral flagella system which is up regulated in SS9 at elevated pressure as well as the absence of 3 phage-related regions from 3TCK and 4 phage-related regions from DSJ4.

1. Vezzi, A., et al., Life at depth: Photobacterium profundum genome sequence and expression analysis. Science, 2005. 307(5714): p. 1459-61.2. Nogi, Y., N. Masui, and C. Kato, Photobacterium profundum sp. nov., a new, moderately barophilic bacterial species isolated from a deep-sea sediment. Extremophiles, 1998. 2(1): p. 1-7.3. DeLong, E.F., Adaptation of deep-sea bacterium to the abyssal environment 1986.4. Campanaro, S., et al., Laterally transferred elements and high pressure adaptation in Photobacterium profundum strains. BMC Genomics, 2005. 6: p. 122.5. Allen, E.E., D. Facciotti, and D.H. Bartlett, Monounsaturated but not polyunsaturated fatty acids are required for growth of the deep-sea bacterium Photobacterium profundum SS9 at high pressure and low temperature. Appl Environ Microbiol, 1999. 65(4): p. 1710-20.6. Bartlett, D.H. and T.J. Welch, ompH gene expression is regulated by multiple environmental cues in addition to high pressure in the deep-sea bacterium Photobacterium species strain SS9. J Bacteriol, 1995. 177(4): p. 1008-16.