首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Salinity responses of the juvenile penaeid shrimp Penaeus japonicus: II. Free amino acids
Institution:1. Department of Ocean Sciences, 0 Marine Lab Road, Memorial University, St John''s, NL A1C 5S7, Canada;2. Bamfield Marine Sciences Centre, Bamfield, BC V0R 1B0, Canada;3. Cape Eleuthera Institute, PO Box EL-26029, Rock Sound, Eleuthera, Bahamas;1. Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko-shi, Chiba-ken 270-1194, Japan;2. Laboratory of Marine Symbiotic Biology, Faculty of Education, Kochi University, 2-5-1 Akebono, Kochi-shi, Kochi-ken 780-8520, Japan
Abstract:The free amino acids (FAA) of juvenile Penaeus japonicus were measured after 48 h of exposure of the shrimps to hypo- and hyperosmotic salinity stress. The concentrations of FAA decreased linearly with decreasing salinity from 50‰ to 10‰. The highest amounts of individual FAA in seawater-adapted P. japonicus are exhibited by glycine (51%), followed by taurine (14%), arginine (10%), proline (9%), and alanine (6%). The main osmoeffectors are glycine, proline, and alanine, which together lower the FAA pool by 80% after a hypoosmotic shock from 40 to 10‰. The concentrations of taurine, arginine, ornithine, and glutamate are not affected by external salinity change. Under hypoosmotic conditions taurine, glutamate, and arginine decrease by only 13–15%, and asparate, ornithine, and lysine by 28–34%. All other amino acids in the FAA pool are reduced by 50 to 88% — the greatest loss is shown by proline (by 96%). Below 25‰ intracellular volume regulation is maintained entirely by proline and glycine, whereas the other FAA concentrations remain more or less constant. After hyperosmotic shock, the concentrations of nearly all FAA increase. This is also true for the essential FAA (+ 86%) — indicating protein hydrolysis. A salinity range between 25 and 40‰ is recommended for the extensive aquaculture of P. japonicus.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号