Ej. O'Loughlin et al., Biodegradation of 2-methyl, 2-ethyl, and 2-hydroxypyridine by an Arthrobacter sp isolated from subsurface sediment, BIODEGRADAT, 10(2), 1999, pp. 93-104
A bacterium capable of degrading 2-methylpyridine was isolated by enrichmen
t techniques from subsurface sediments collected from an aquifer located at
an industrial site that had been contaminated with pyridine and pyridine d
erivatives. The isolate, identified as an Arthrobacter sp., was capable of
utilizing 2-methylpyridine, 2-ethylpyridine, and 2-hydroxypyridine as prima
ry C, N, and energy sources. The isolate was also able to utilize 2-, 3-, a
nd 4-hydroxybenzoate, gentisic acid, protocatechuic acid and catechol, sugg
esting that it possesses a number of enzymatic pathways for the degradation
of aromatic compounds. Degradation of 2-methylpyridine, 2-ethylpyridine, a
nd 2-hydroxypyridine was accompanied by growth of the isolate and release o
f ammonium into the medium. Degradation of 2-methylpyridine was accompanied
by overproduction of riboflavin. A soluble blue pigment was produced by th
e isolate during the degradation of 2-hydroxypyridine, and may be related t
o the diazadiphenoquinones reportedly produced by other Arthrobacter spp. w
hen grown on 2-hydroxypyridine. When provided with 2-methylpyridine, 2-ethy
lpyridine, and 2-hydroxypyridine simultaneously, 2-hydroxypyridine was rapi
dly and preferentially degraded; however there was no apparent biodegradati
on of either 2-methylpyridine or 2-ethylpyridine until after a seven day la
g. The data suggest that there are differences between the pathway for 2-hy
droxypyridine degradation and the pathway(s) for 2-methylpyridine and 2-eth
ylpyridine.