qPCR-Based Monitoring of 2-Methylisoborneol/Geosmin-Producing Cyanobacteria in Drinking Water Reservoirs in South Korea [PDF]
Cyanobacteria can exist in water resources and produce odorants. 2-Methylisoborneol (2-MIB) and geosmin are the main odorant compounds affecting the drinking water quality in reservoirs.
Jung Eun Lee +4 more
doaj +3 more sources
Dehydration products of 2-methylisoborneol [PDF]
Abstract 2-Methylenebornane and 2-methyl-2-bornene have previously been identified as dehydration or degradation products of 2-methylisoborneol (MIB), a compound responsible for taste and odour problems in various water environments. Previously, the identification of these products has been based on mass spectral analysis only. The dehydration of MIB
Laura Drummond +2 more
europepmc +10 more sources
Biosynthesis of 2-Methylisoborneol in Cyanobacteria [PDF]
The production of odiferous metabolites, such as 2-methlyisoborneol (MIB), is a major concern for water utilities worldwide. Although MIB has no known biological function, the presence of the earthy/musty taste and odor attributed to this compound result in the reporting of numerous complaints by consumers, which undermines water utility performance ...
S, Giglio +4 more
openaire +4 more sources
An automated micro solid phase extraction gas chromatography–mass spectrometry (μSPE-GC–MS) detection method for geosmin and 2-methylisoborneol in drinking water [PDF]
Geosmin and 2-methylisoborneol (2-MIB) are amongst the most common earthy and musty taste and odour (T&O) compounds found in drinking water. With low odour threshold detection limits below 10 ng L^−1, and the complexity of raw water matrices, these two ...
R. Bristow +6 more
semanticscholar +2 more sources
Genomics insights into production of 2-methylisoborneol and a putative cyanobactin by Planktothricoides sp. SR001 [PDF]
Planktothricoides is a free-living filamentous cyanobacterium belonging to the order Oscillatoriales and the family Phormidiaceae, capable of forming bloom in fresh and brackish waters.
Shu Harn Te +4 more
doaj +2 more sources
Biotransformations of 2-Methylisoborneol by Camphor-Degrading Bacteria [PDF]
ABSTRACTMany camphor-degrading bacteria that are able to transform 2-methylisoborneol (2-MIB) have been identified. Three of these strains have been examined in detail.Rhodococcus ruberT1 metabolizes camphor through 6-hydroxycamphor but converts 2-MIB to 3-hydroxy-2-MIB.Pseudomonas putidaG1, which metabolizes camphor through 5-hydroxycamphor, converts ...
Richard W, Eaton, Peter, Sandusky
openaire +3 more sources
eDNA- and eRNA-Based Detection of 2-Methylisoborneol-Producing Cyanobacteria and Intracellular Synthesis Dynamics in Freshwater Ecosystem [PDF]
Taste and odor (T&O) compounds in freshwater are frequently produced by certain cyanobacteria; however, their occurrence remains difficult to predict.
Keonhee Kim +3 more
doaj +2 more sources
Heterologous expression of mtf and mtc genes of Pseudanabaena foetida var. intermedia is sufficient to produce 2-methylisoborneol in Escherichia coli [PDF]
Microbial volatile metabolite 2-methylisoborneol (2-MIB) causes odor and taste issues in drinking water, making it unappealing for human consumption. It has been suggested that 2-MIB biosynthesis consists of two main steps, namely, methylation of geranyl
Kaushalya Dayarathne +8 more
semanticscholar +2 more sources
Ultrasonically induced degradation of 2-methylisoborneol and geosmin [PDF]
2-Methylisoborneol (MIB) and geosmin (GSM) are taste and odor compounds produced by cyanobacteria in surface waters. While the strong odors and musty flavors of MIB and GSM are generally associated with poor water quality, the removal of these semi-volatile compounds presents a significant challenge to drinking water providers. Likewise in aquaculture,
Weihua, Song, Kevin E, O'Shea
openaire +3 more sources
Heterologous expression of 2-methylisoborneol / 2 methylenebornane biosynthesis genes in Escherichia coli yields novel C11-terpenes. [PDF]
The structural diversity of terpenoids is limited by the isoprene rule which states that all primary terpene synthase products derive from methyl-branched building blocks with five carbon atoms.
Max J Kschowak +4 more
doaj +2 more sources

