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Lipoxygenase activity in the oomyceteSaprolegnia is dependent on environmental cues and reproductive competence
Institution:1. International Centre for Aquaculture Research and Development (ICARD) and the Aberdeen Oomycete Laboratory, University of Aberdeen, Institute of Medical Sciences, Foresterhill, Aberdeen, AB25 2ZD, UK;2. Department of Pathology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh, 2202, Bangladesh;3. Fish Health and Welfare, Salmon and Fresh Water Fisheries, Marine Scotland Science (MSS), Aberdeen, AB11 9DB, UK;1. Laboratoire de Recherche en Sciences Végétales, Université de Toulouse, CNRS, UPS, 24 Chemin de Borde Rouge, Auzeville, BP42617, 31326 Castanet-Tolosan, France;2. Department for Innovation in Biological, Agro-Food and Forest Systems, University of Tuscia, Viterbo, Italy;3. Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Box 190 234 22 Lomma, Sweden;4. Department of Plant and Soil Science, School of Biological Sciences, University of Aberdeen, Aberdeen, AB24 3UU Scotland, UK;5. International Centre for Aquaculture Research and Development (ICARD), Aberdeen Oomycete Laboratory, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, AB25 2ZD Scotland, UK
Abstract:Saprolegnia ferax grows vegetatively when not nutrient limited; however, when starved, it switches to sexual reproduction.Saprolegnia parasitica does not show this reproductive competence in response to starvation. This study examined lipoxygenase activity inS. ferax andS. parasitica during starvation. Lipoxygenase activity in starved cultures ofS. ferax decreased in a time-dependent manner, reaching less than 20% of initial levels by 72 h and decreasing to less than 10% by 192 h, the onset of reproductive structures.S. ferax showed no decline in peroxidase activity over 72 h of starvation.S. parasitica had initial lipoxygenase activity 50% greater thanS. ferax and showed no decline in lipoxygenase activity during 72 h of starvation and only a small decline at 192 h. StarvedS. ferax cultures resumed vegetative growth after transfer back to rich medium, and lipoxygenase activity returned to 70–80% of initial levels after 24 h in rich medium.S. ferax cultures transferred to full-strength medium maintained initial lipoxygenase activity levels for 48 h, then showed a sharp decrease between 48 and 72 h, the time at which nutrients become limiting. Cultures transferred to 40 and 20% strength media showed more rapid declines in lipoxygenase activity. These data demonstrate that starvation, an environmental cue that initiates sexual reproduction, depresses lipoxygenase activity in the reproductively competentS. ferax but not in the reproductively recalcitrantS. parasitica. These data are consistent with the hypothesis that lipoxygenase products are associated with vegetative growth but not sexual reproduction.
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