Among
monoaromatic hydrocarbons, xylenes, especially
the ortho and para isomers, are
the least biodegradable
compounds in oxygen-limited subsurface environments. Although much
knowledge has been gained regarding the anaerobic degradation of xylene
isomers in the past 2 decades, the diversity of those bacteria which
are able to degrade them under microaerobic conditions is still unknown.
To overcome this limitation, aerobic and microaerobic xylene-degrading
enrichment cultures were established using groundwater taken from
a xylene-contaminated site, and the associated bacterial communities
were investigated using a polyphasic approach. Our results show that
the xylene-degrading bacterial communities were distinctly different
between aerobic and microaerobic enrichment conditions. Although members
of the genus Pseudomonas were the most
dominant in both types of enrichments, the Rhodoferax and Azovibrio lineages were only
abundant under microaerobic conditions, while Sphingobium entirely replaced them under aerobic conditions. Analysis of a metagenome-assembled
genome of a Rhodoferax-related bacterium
revealed aromatic hydrocarbon-degrading ability by identifying two
catechol 2,3-dioxygenases in the genome. Moreover, phylogenetic analysis
indicated that both enzymes belonged to a newly defined subfamily
of type I.2 extradiol dioxygenases (EDOs). Aerobic and microaerobic
xylene-degradation experiments were conducted on strains Sphingobium sp. AS12 and Pseudomonas sp. MAP12, isolated from the aerobic and microaerobic enrichments,
respectively. The obtained results, together with the whole-genome
sequence data of the strains, confirmed the observation that members
of the genus Sphingobium are excellent
aromatic hydrocarbon degraders but effective only under clear aerobic
conditions. Overall, it was concluded that the observed differences
between the bacterial communities of aerobic and microaerobic xylene-degrading
enrichments were driven primarily by (i) the method of aromatic ring
activation (monooxygenation vs dioxygenation), (ii) the type of EDO
enzymes, and (iii) the ability of degraders to respire utilizing nitrate.