Abstract
To allow to discriminate rapidly the strains of Porphyra tenera var. tamatsuensis, cultivars of which grow more vigorously than strains of P. tenera var. tenera, strains of both varieties were examined by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis using mitochondrial DNA related to the ATP synthase F0 subunit 6 (ATP6) gene. The lengths of all sequences in this region of three strains of each variety were 670 bp and had just a single nucleotide substitution. Digestion with the restriction enzyme of TaaI yielded three visible bands which appeared in the three strains of P. tenera var. tamatsuensis, whereas two bands appeared in the three strains of P. tenera var. tenera. We therefore conclude that PCR-RFLP analysis is a valuable tool for discrimination of P. tenera var. tamatsuensis among the stock of P. tenera strains used for mariculture.
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Acknowledgments
The authors wish to express our thanks to Dr. Kyosuke Niwa, Fisheries Technology Institute, Hyogo Prefectural Technology Center for Agriculture, Forestry and Fisheries for valuable advice in this study. We also thank Kabashima Suisan, Ariakekai Laboratory, Fukuoka Fisheries and Marine Technology Research Center, Kumamoto Prefectural Fisheries Research Center, Yamaguchi Prefectural Fisheries Research Center, Inland Sea Research Division, National Research Institute of Fisheries and Environment of Inland Sea, Fisheries Research Agency and Professor Miyuki Maegawa, Graduate School of Bioresources, Mie University for collecting samples.
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Abe, M., Kobayashi, M., Tamaki, M. et al. Rapid discrimination of Porphyra tenera Kjellman var. tamatsuensis Miura by PCR-RFLP. J Appl Phycol 22, 405–408 (2010). https://doi.org/10.1007/s10811-009-9472-3
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DOI: https://doi.org/10.1007/s10811-009-9472-3