Abstract:
:The purpose of this research was to pursuit the quantification of microbial degradation capacity for 2,4-dichlorophenoxyacetic acid (2,4-D) by detecting and quantifying a prominent 2,4-D degradation encoding plasmid. Batch reactor acclimation, de-acclimation, and re-acclimation tests were conducted during which periods the courses of 2,4-D dissipation and plasmid evolution were quantitatively measured. Pure cultures of bacterial strains were detected to give rise to a plasmid approximately the size of 90 kb after acclimation. The 90 kb plasmid content of Arthrobacter sp. increased when degradation occurred after acclimation, with a rate that corresponded closely to the degradation rate. During de-acclimation, plasmid content declined exponentially at a half-life of approximately 3.5 days. Re-acclimation saw a renewed induction of plasmid, but substrate consumption limited the rise of plasmid to a level much lower than after the first acclimation. This research recommends a method for measuring the microbial degradation capability for a xenobiotic.
journal_name
Bioresour Technoljournal_title
Bioresource technologyauthors
Chong NM,Chang HWdoi
10.1016/j.biortech.2008.09.016subject
Has Abstractpub_date
2009-02-01 00:00:00pages
1174-9issue
3eissn
0960-8524issn
1873-2976pii
S0960-8524(08)00772-4journal_volume
100pub_type
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doi:10.1016/j.biortech.2006.05.044
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