Process performances of an upflow anaerobic filter treating olive mill wastewater and the response of methanogenic Archaea to increasing volumetric organic load (VOL) were studied. At a VOL of 15 g chemical oxygen demand (COD) L-1 day 90% of the influent COD was removed. Following a VOL increase from 6 to 15 g COD L-1 day(-1), the polymerase chain reaction (PCR) titre of hydrogenotrophic Methanobacterium, determined by magnetic capture of the target DNA and group-specific PCR based on the 16S rRNA gene, decreased from 10(11) to 10(8) cells g(-1) sludge, while that of Methanomicrobiaceae and relatives increased from 10(4) to 10(6) cells g(-1) sludge. Methanosaeta-like acetoclastic methanogens were less affected by VOL variation and dominated at high VOL with a 16S rRNA gene PCR titre of 10(9) cells g(-1) sludge. Single-strand conformation polymorphism analysis of the PCR-amplified archaeal 16S rRNA gene showed a stable band pattern, indicating that VOL variation affected the methanogen PCR titre but not the archaeal community structure. (c) 2006 Society of Chemical Industry.
Response of methanogen populations to organic load increase during anaerobic digestion of olive mill wastewater / A. Rizzi, M. Zucchi, S. Borin, M. Marzorati, C. Sorlini, D. Daffonchio. - In: JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY. - ISSN 0268-2575. - 81:9(2006 Sep), pp. 1556-1562. [10.1002/jctb.1558]
Response of methanogen populations to organic load increase during anaerobic digestion of olive mill wastewater
A. Rizzi;S. Borin;M. Marzorati;C. Sorlini;D. Daffonchio
2006
Abstract
Process performances of an upflow anaerobic filter treating olive mill wastewater and the response of methanogenic Archaea to increasing volumetric organic load (VOL) were studied. At a VOL of 15 g chemical oxygen demand (COD) L-1 day 90% of the influent COD was removed. Following a VOL increase from 6 to 15 g COD L-1 day(-1), the polymerase chain reaction (PCR) titre of hydrogenotrophic Methanobacterium, determined by magnetic capture of the target DNA and group-specific PCR based on the 16S rRNA gene, decreased from 10(11) to 10(8) cells g(-1) sludge, while that of Methanomicrobiaceae and relatives increased from 10(4) to 10(6) cells g(-1) sludge. Methanosaeta-like acetoclastic methanogens were less affected by VOL variation and dominated at high VOL with a 16S rRNA gene PCR titre of 10(9) cells g(-1) sludge. Single-strand conformation polymorphism analysis of the PCR-amplified archaeal 16S rRNA gene showed a stable band pattern, indicating that VOL variation affected the methanogen PCR titre but not the archaeal community structure. (c) 2006 Society of Chemical Industry.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.