Unknown

Dataset Information

0

Purification and properties of the enzyme arylamine N-acetyltransferase from the housefly Musca domestica.


ABSTRACT: The enzyme arylamine N-acetyltransferase (ANAT) from the housefly (Musca domestica) has been purified. The M(r) of the purified enzyme was 27,600 +/- 1700 as estimated by gel filtration. SDS/PAGE yielded a value of 26,000 +/- 300, clearly indicating a monomeric structure. The purified enzyme had apparent Km values for acetyl-CoA and tyramine of 8.4 microM and 8.8 microM respectively, a pH optimum of 7.2 in 10 mM potassium phosphate buffer and an apparent pI of 5.8. ANAT activity showed a strong dependency on the presence of 2-mercaptoethanol during the purification stages. The enzyme could be completely inactivated by treatment with p-chloromercuribenzoate although the enzyme activity was protected by preincubation with acetyl-CoA. One or more cysteine residues are clearly required for catalytic activity, as demonstrated for the mammalian enzyme. In contrast, partial sequencing of the enzyme has yielded a number of peptide sequences, including the N-terminal sequence, which show no similarity with those reported for the mammalian and avian enzymes.

SUBMITTER: Whitaker DP 

PROVIDER: S-EPMC1134831 | biostudies-other | 1993 Oct

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC7217826 | biostudies-literature
| S-EPMC1138070 | biostudies-other
| S-EPMC6104014 | biostudies-literature
| S-EPMC8552782 | biostudies-literature
2017-06-13 | GSE88939 | GEO
| S-EPMC1217095 | biostudies-other
| S-EPMC10450350 | biostudies-literature
| S-EPMC5734023 | biostudies-literature
| S-EPMC5503848 | biostudies-literature
| S-EPMC5381375 | biostudies-literature