Abstract:
:Glycerol has the potential of being a low-cost and extremely versatile building block. However, current transformation strategies such based on noble-metal-catalysts show several disadvantages including catalyst deactivation or negative environmental impacts. In this study glycerol was oxidized by 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) in the presence of laccase from Trametes hirsuta. Analysis of the reaction production indicated sequential oxidation to glyceraldehyde, glyceric acid and tartronic acid, finally resulting in mesoxalic acid. The number and nature of oxidation products was depended on the concentration of TEMPO used. At lower TEMPO concentrations (<6mM) the major initial reaction product was glyceraldehyde while at higher concentration in addition considerable amounts of glyceric acid were formed. Glycerol oxidation was also shown with laccase immobilised on alumina pellets which increased laccase stability.
journal_name
Bioresour Technoljournal_title
Bioresource technologyauthors
Liebminger S,Siebenhofer M,Guebitz Gdoi
10.1016/j.biortech.2009.04.051subject
Has Abstractpub_date
2009-10-01 00:00:00pages
4541-5issue
20eissn
0960-8524issn
1873-2976pii
S0960-8524(09)00469-6journal_volume
100pub_type
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