Two PCR-amplified genomic DNA fragments encoding apple (cv. Fuji) polyphenol oxidase (PPO) were cloned and sequenced. A comparison of genomic DNA with cDNAs revealed that the PPOs lacked introns. Both PPO DNAs appear to encode a 66-kDa precursor protein consisting of a 56-kDa mature protein and a N-terminal transit peptide of 10-kDa N-terminal transit peptide. Apple PPO DNA was expressed in Escherichia coli, and the gene product (56 kDa) without a transit peptide was immunochemically detected and was the same size (ca. 65 kDa) as the main PPO of apple fruit by SDS-PAGE. © 1998, Taylor & Francis Group, LLC. All rights reserved.
CITATION STYLE
Haruta, M., Murata, M., Hiraide, A., Kadokura, H., Yamasaki, M., Sakuta, M., & Shimizu, S. (1998). Cloning genomic dna encoding apple polyphenol oxidase and comparison of the gene product in escherichia coli and in apple. Bioscience, Biotechnology and Biochemistry, 62(2), 358–362. https://doi.org/10.1271/bbb.62.358
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