1980
DOI: 10.1007/bf00016235
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Aquatic Microbiology with Reference to Tannin Degradation

Abstract: Tannins in aquatic environment cause harmful effects to aquatic life. They are inhibitory to microbial growth, respiration and metabolism. A few microorganisms degrade tannins and the factors influencing degradation are discussed. The need for coordinated approach is emphasized.

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Cited by 28 publications
(14 citation statements)
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References 21 publications
(13 reference statements)
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“…Previous studies of Myriophyllum-associated bacteria focused on potential pathogens useful for the biological control of M. spicatum (Chand et al 1992) or on rhizosphere bacteria involved in nitrogen metabolism (Blotnick et al 1980). So far, the majority of studies focusing on tannin-degrading bacteria are either from environments exposed to industrial tannery waste (Chowdhury et al 2004, Franco et al 2005 or from investigations of intestinal bacteria in tannin-feeding invertebrates and vertebrates (Goel et al 2005, Smith et al 2005, while little evidence exists for such specialised bacteria in natural waters, most of them from anaerobic environments (Mahadevan & Muthukumar 1980, Schink et al 2000. In contrast to other major submerged aquatic angiosperms, M. spicatum produces and releases high concentrations of hydrolysable polyphenols (Smolders et al 2000, Choi et al 2002, Gross 2003.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies of Myriophyllum-associated bacteria focused on potential pathogens useful for the biological control of M. spicatum (Chand et al 1992) or on rhizosphere bacteria involved in nitrogen metabolism (Blotnick et al 1980). So far, the majority of studies focusing on tannin-degrading bacteria are either from environments exposed to industrial tannery waste (Chowdhury et al 2004, Franco et al 2005 or from investigations of intestinal bacteria in tannin-feeding invertebrates and vertebrates (Goel et al 2005, Smith et al 2005, while little evidence exists for such specialised bacteria in natural waters, most of them from anaerobic environments (Mahadevan & Muthukumar 1980, Schink et al 2000. In contrast to other major submerged aquatic angiosperms, M. spicatum produces and releases high concentrations of hydrolysable polyphenols (Smolders et al 2000, Choi et al 2002, Gross 2003.…”
Section: Discussionmentioning
confidence: 99%
“…Müller et al (2007) were the first to show that distinct bacterial groups isolated from the biofilm and the surrounding water column of the allelopathically active submerged macrophyte M. spicatum are able to degrade polyphenolic allelochemicals. This was surprising as polyphenols are known for their anti-bacterial properties (Walenciak et al, 2002), and polyphenol degrading bacteria were only known from anaerobic environments (Mahadevan and Muthukumar, 1980;Schink et al, 2000). Specialized bacteria in the vicinity of allelopathically active submerged macrophytes might be thus one reason for the rapid disappearance of allelochemicals from the water column.…”
Section: Iiii Factors Influencing Sensitivities Of Algae To Allelocmentioning
confidence: 99%
“…However, the impacts of R. mangle invasion on benthic ecosystem functioning, in particular, how mangroves modify sediment metabolism and C-remineralization processes in the Hawaiian coastal zone, remain essentially unexplored. Rhizophora mangle detritus is rich in tannins, which can be toxic to benthic detritivores, interfering with digestive enzymes (Mahadevan and Muthukumar, 1980;Neilson et al, 1986;Alongi, 1987;Sessegolo and Lana, 1991). Therefore, we postulate that mangrove invasion will favor microbial C-remineralization processes by limiting macrofaunal consumption and assimilation of detrital carbon (Alongi, 1987;Tietjen and Alongi, 1990;Robertson et al, 1992).…”
mentioning
confidence: 95%