z-logo
open-access-imgOpen Access
Diversity of catechol 2,3‐dioxygenase genes of bacteria responding to dissolved organic matter derived from different sources in a eutrophic lake
Author(s) -
Kasuga Ikuro,
Nakajima Fumiyuki,
Furumai Hiroaki
Publication year - 2007
Publication title -
fems microbiology ecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.377
H-Index - 155
eISSN - 1574-6941
pISSN - 0168-6496
DOI - 10.1111/j.1574-6941.2007.00347.x
Subject(s) - biology , microcosm , dissolved organic carbon , eutrophication , bacteria , dioxygenase , library , gene , catechol , humus , microbiology and biotechnology , environmental chemistry , botany , biochemistry , ecology , genetics , nutrient , 16s ribosomal rna , chemistry , soil water
Catechol 2,3‐dioxygenase (C23O) is an extradiol dioxygenase that plays an important role in degrading aromatic compounds such as those found at polluted sites. However, little is known about the diversity of C23O genes in unpolluted environments. In such environments, various factors, including the quality and quantity of dissolved organic matter (DOM), could influence the composition and behaviour of bacterial community possessing C230 genes. We investigated C23O genes in bacteria responding to DOM from various sources in a eutrophic lake by PCR and cloning. Six microcosms filled with lake water containing indigenous bacteria and DOM from different sources were incubated for 10 days. After 1 or 2 days of incubation, C23O genes were detected in the microcosms enriched with DOM recovered from inflow river water and humus from reed grass. The sequences were very diverse but had features conserved in extradiol dioxygenases. The clone libraries generated on day 2 showed distinctive compositions among microcosms, indicating that bacteria possessing a variety of C23O genes responded differently to DOM from different sources. After 10 days of incubation, C23O genes in a previously unidentified gene cluster, ‘Cluster X’, became dominant in the libraries.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here