Development of tyrosine aminotransferase and para-hydroxyphenylpyruvate dioxygenase activities in fetal and neonatal human liver.
Open Access
- 1 July 1982
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 70 (1) , 198-200
- https://doi.org/10.1172/jci110593
Abstract
In livers of fetuses of 220--340 g body wt, total cytosolic tyrosine aminotransferase activity was 1.0 nmol of product/mg of protein per min, and the corresponding values for autopsy livers of newborns of 740--1,475 g and 2,600--3,650 g were 1.5 and 5.7, respectively, as compared with the adult value of 12.7. On the other hand, para-hydroxyphenylpyruvate dioxygenase activity is at adult level already in fetuses less than 340 g body wt. The Km value for tyrosine of tyrosine aminotransferase (1 mM) was considerably higher than the corresponding value for para-hydroxyphenylpyruvate of para-hydroxyphenylpyruvate dioxygenase (50 micro M). These results suggest that tyrosine aminotransferase is the rate limiting enzyme in the catabolism of tyrosine in premature infants.This publication has 15 references indexed in Scilit:
- Tyrosine aminotransferase as the rate‐limiting step for tyrosine catabolism in isolated rat liver cellsFEBS Letters, 1981
- CSF Neurotransmitter StudiesAmerican Journal of Diseases of Children, 1980
- Regulation of the tyrosine oxidizing system in fetal rat liverArchives of Biochemistry and Biophysics, 1980
- Tyrosine and its metabolites in urine and serum of premature and mature newborns: Increased values during formula versus breast feedingEuropean Journal of Pediatrics, 1979
- Heterogeneity of Hepatic Tyrosine Aminotransferase. Separation of the Multiple Forms from Rat and Frog Liver by Isoelectric Focussing and Hydroxylapatite Column Chromatography and Their Partial Characterization.Acta Chemica Scandinavica, 1976
- Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependentClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- The origin of urinary p-hydroxyphenylpyruvate in a patient with hepatic cytosol tyrosine aminotransferase deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- Purification of p-Hydroxyphenylpyruvate Hydroxylase from Human Liver.Acta Chemica Scandinavica, 1971
- Ascorbic Acid, a Coenzyme in Tyrosine OxidationScience, 1951
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951