Biodegradability and toxicity of monorhamnolipid biosurfactant diastereomers

Synthetic monorhamnolipids differ from biologically produced material because they are produced as single congeners, depending on the β-hydroxyalkanoic acid used during synthesis. Each congener is produced as one of four possible diastereomers resulting from two chiral centers at the carbinols of th...

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Bibliografiska uppgifter
I publikationen:J Hazard Mater
Huvudupphovsmän: Hogan, David E., Tian, Fei, Malm, Scott W., Olivares, Christopher, Pacheco, Ricardo Palos, Simonich, Michael T., Hunjan, Anoop S., Tanguay, Robert L., Klimecki, Walter T., Polt, Robin, Pemberton, Jeanne E., Curry, Joan E., Maier, Raina M.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2018
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6289288/
https://ncbi.nlm.nih.gov/pubmed/30390580
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhazmat.2018.10.050
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