1. It was recognized that intact cells and dried cells of
Saccharomyces saké could not oxidize glycerol. This seems to be resulted from the slow velocity of the following two reactions:
glycerol → glycerophosphate
and glycerophosphate → triose phosphate.
2.
Hansenula anomala can oxidize glycerol, glycerophosphate and other poly alcohols. In the earlier stage of glycerol-oxidation, the rate was accelerated by inorganic phosphate and diphosphopyridine nucleotide. A cell-free enzyme solution from the autolyzed cells contained glycerokinase which transfers phosphate from ATP to glycerol and glycerophosphatase which splits phosphate from glycerophosphate. Therefore, the authors propose that the phosphorylation of glycerol as the first reaction of glycerol-oxidation couples
in vivo with diphosphopyridine nucleotide, and that the first metabolite is glycerophosphate.
3. It was unsuccessful to extract enzymes which oxidize glycerol from
H. anomala, but it was recognized that dried cells and homogenates prepared from them could oxidize glycero-phosphate. As the dried cells of
S. saké can ferment glucose, it is apparent that they contain enzymes which metabolize triose phosphate. And the velocity of glycerophosphate-oxidation by
H. anomala was accelerated by the addition of the minced matter of
S. sake. 4. As metabolites resulting from glycerophosphate-oxidation by the extract of minced matter of intact cells of
H. anomala, pyruvate' and
a-ketoglutarate were found by the method of paper partition chromatography. And
H. anomala could oxidize organic acids in the TCA-cycle; citrate, succinate, fumarate and malate.
5. From these findings, glycerol (via glycerophosphate and triose phosphate) may be oxidized to pyruvate and finally to CO
2 through the TCA-cycle by
H. anomala. In this case, the process via dihydroxyacetone rom glycerol may be unreasonable by the fact that little activity of glycerol dehydrogenase and negligible oxidation of dihydroxyacetone are recognized.
View full abstract