J. Onken et Rg. Berger, Biotransformation of citronellol by the basidiomycete Cystoderma carcharias in an aerated-membrane bioreactor, APPL MICR B, 51(2), 1999, pp. 158-163
The basidiomycete Cystoderma carcharias transformed citronellol into 3,7-di
methyl-1,6,7-octanetriol as the main product. 3,7-Dimethyl-6,7-epoxy-1-octa
nol was identified as important intermediary product of the biotransformati
on, and the allylic diols 2,6-dimethyl-2-octene-1,8-diol, 3,7-dimethyl-5-oc
tene-1,7-diol and 3,7-dimethyl-7-octene-1,6-diol were found to be minor pro
ducts, Microbial formation of rose oxide, a flavour-impact component, was o
bserved for the first time. The formation of the main products was inhibite
d by 70% after addition of 0.1 mmol 1(-1) cytochrome monooxygenase inhibito
rs. Formation of 3,7-dimethyl-1,6,7-octanetriol was effective in a bioreact
or with aeration over a coil of a hydrophobic microporous polypropene capil
lary membrane. Production rates of up to 150 mg 1(-1) day(-1) were reached
and led to a product concentration of 866 mg 1(-1) (conversion rate: 52%).
The total loss of the added volatile substrate via the exhaust air was 4.5%
when this aeration method was used.