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1.
Bioresour Technol ; 206: 275-278, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26883059

ABSTRACT

The kinetic parameters of isoprene biodegradation were studied in a bioreactor, comprising of bioscrubber and polyurethane foam packed biofilter in series and inoculated with Pseudomonas sp., using a Michaelis-Menten type model. The maximum elimination capacity, ECmax; substrate constant, Ks and ECmax/Ks values for bioscrubber were found to be 666.7 g m(-3) h(-1), 9.86 g m(-3) and 67.56 h(-1), respectively while those for biofilter were 3333 g m(-3) h(-1), 13.96 g m(-3) and 238.7 h(-1), respectively. The biofilter section exhibited better degradation efficiency compared to the bioscrubber unit. Around 62-75% of the feed isoprene got converted to carbon dioxide, indicating the efficient capability of bacteria to mineralize isoprene. The FTIR and GC-MS analyses of degradation products indicated oxidative cleavage of unsaturated bond of isoprene. These results were used for proposing a plausible degradation pathway for isoprene.


Subject(s)
Butadienes/metabolism , Hemiterpenes/metabolism , Metabolome , Pentanes/metabolism , Biodegradation, Environmental , Bioreactors , Carbon/analysis , Filtration/instrumentation , Gas Chromatography-Mass Spectrometry , Kinetics , Pseudomonas/metabolism , Spectroscopy, Fourier Transform Infrared
2.
FEMS Microbiol Ecol ; 82(1): 118-34, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22587395

ABSTRACT

The diversity and density of methanogenic archaea and methane production were investigated ex situ at different growth stages of rice plant cultivated in compost-treated tropical rice fields. The qPCR analysis revealed variation in methanogens population from 3.40 × 10(6) to 1.11 × 10(7)  copies g(-1)  dws, in the year 2009 and 4.37 × 10(6) to 1.36 × 10(7)  copies g(-1)  dws in the year 2010. Apart from methanogens, a large number of bacterial (9.60 × 10(9) -1.44 × 10(10)  copies g(-1)  dws) and archaeal (7.13 × 10(7) -3.02 × 10(8)  copies g(-1)  dws) communities were also associated with methanogenesis. Methanogen population size varied in the order: flowering > ripening > tillering > postharvest > preplantation stage. The RFLP-based 16S rRNA gene-targeted phylogenetic analysis showed that clones were closely related to diverse group of methanogens comprising members of Methanomicrobiaceae, Methanosarcinaceae, Methanosaetaceae and RC I. Laboratory incubation studies revealed higher amount of cumulative CH(4) at the flowering stage. The integration of methanogenic community structure and CH(4) production potential of soil resulted in a better understanding of the dynamics of CH(4) production in organically treated rice-field soil. The hypothesis that the stages of plant development influence the methanogenic community structure leading to temporal variation in the CH(4) production has been successfully tested.


Subject(s)
Methane/biosynthesis , Methanomicrobiaceae/classification , Methanosarcinaceae/classification , Methanosarcinales/classification , Oryza/microbiology , Soil Microbiology , Agriculture/methods , DNA, Archaeal/genetics , Methanomicrobiaceae/genetics , Methanosarcinaceae/genetics , Methanosarcinales/genetics , Oryza/growth & development , Phylogeny , Polymorphism, Restriction Fragment Length , Population Density , RNA, Ribosomal, 16S/genetics , Soil/chemistry
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