Pallini R, Martelli P, Bardelli A M, Guazzi G C, Federico A
Istituto di Scienze Neurologiche, Università di Siena, Italy.
Neurology. 1987 Dec;37(12):1878-80. doi: 10.1212/wnl.37.12.1878.
The thiosulfate:cyanide sulfurtransferase (rhodanese) enzyme (EC 2.8.1.1.) was studied in human leukocytes from control subjects and from nine patients with Leber's hereditary optic atrophy. Enzyme activity was proportional to protein concentration in the tested range (0.09 to 0.39 mg) as well as to incubation time. The optimal pH for reaction was 8.7 and the apparent Km for thiosulfate was 7 X 10(-3) M. No significant difference of enzyme activity was present in Leber's disease.