Abstract
Secretory granules of hatching gland were isolated from a 0.3 M sucrose homogenate of whole medaka embryos at prehatching stage by differential centrifugation followed by a Percoll density gradient centrifugation. The obtained preparation was almost free of melanosomes and composed exclusively of the secretory granules of hatching gland (hatching enzyme granules), as judged by morphological and as enzymological criteria. Aqueous extracts of the purified secretory granules showed a specific choriolytic activity as high as .apprx. 40 times that of a partially purified secretory granule preparation, P1000, and represented a single protein band with MW of .apprx. 21,000 on SDS[sodium dodecylsulfate]-polyacrylamide gel electrophoresis. A major component of the hatching enzyme preparation (PII-0.3 enzyme, 13) purified from the hatching liquid was identical with the 21,000 MW band. Apparently, the hatching enzyme is present in the secretory granules of prehatching embryos in an active molecular form.