[Objectives]To study the differences of growth rate,morphology,ultrastructure,pigment content and antioxidant enzyme activity of free-living conchocelis of cultivated type of Neopyropia yezoensis under different light...[Objectives]To study the differences of growth rate,morphology,ultrastructure,pigment content and antioxidant enzyme activity of free-living conchocelis of cultivated type of Neopyropia yezoensis under different light qualities(white,red,blue,and green light).[Methods]The study was carried out through light quality design and culture,growth rate determination,microstructure and ultrastructure observation,chlorophyll a content and carotenoid content determination,phycobiliprotein content determination,malondialdehyde(MDA)content determination,superoxide dismutase(SOD)activity determination.[Results]After 21 d of culture,the specific growth rate(SGR)and chlorophyll a content of free-living conchocelis of N.yezoensis were significantly increased by white light(WL),followed by red light(RL)and green light(GL),and they were the lowest under blue light(BL).Compared with the WL group,the BL group had the highest content of phycoerythrin(PE),and the RL and GL groups had the highest content of phycocyanin(PC).The algal body of WL group was normal black brown,and the cell wall was the thickest.In RL and GL groups,the algal bodies were green,and their diameters and cell wall thicknesses were similar to those in WL group.In BL group,the algal body was bright red,the diameter was the smallest,the cell wall was the thinnest,and the ultrastructure showed that the number of plastoglobulus on the thylakoid was the largest.After BL irradiation,the highest MDA content and the lowest SOD activity were observed.The results revealed that WL is the most beneficial to the growth of free-living conchocelis,followed by RL and GL,while BL has adverse effects.[Conclusions]This study explored the most suitable light quality conditions for the propagation of free-living conchocelis.It is expected to provide germplasm guarantee for the production and seedling of N.yezoensis.展开更多
The cytological characteristics of major green-tide-forming green algae <i>Ulva prolifera</i> collected from Yellow Sea were studied th<span style="white-space:normal;"><span style="...The cytological characteristics of major green-tide-forming green algae <i>Ulva prolifera</i> collected from Yellow Sea were studied th<span style="white-space:normal;"><span style="font-family:;" "="">r</span></span><span style="white-space:normal;"><span style="font-family:;" "="">ough cutting segments, long time low temperature or dark treatments. After </span></span><span style="white-space:normal;"><span style="font-family:;" "="">being </span></span><span style="white-space:normal;"><span style="font-family:;" "="">dried in the shade and preserved at -</span></span><span style="white-space:normal;"><span style="font-family:;" "="">20<span style="white-space:nowrap;">°</span></span></span><span style="white-space:normal;"><span style="font-family:;" "="">C for 30 days, the <i>U.</i> <i>prolifera</i> was cultured at 4<span style="white-space:nowrap;">°</span>C in sterilized seawater under 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> light intensity for 120 days, results indicated that the plastid of <i>U. prolifera</i> continuously shrank with the extension of treatment, and most cells turned white and died, only a small amount of cells still contained a few of visible inclusions at the 120d of treatment. Then those samples were transferred to 20<span style="white-space:nowrap;">°</span>C and 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> condition for recovery cultivation, after about 10 days, some recovery cells were observed in the thallus, and those cells developed to young thallus gradually and released germ cells almost in the same time. After about 60 days of recovery cultivation, the newly-grown green thallus broke through the original dead thallus, and the germ cells also grew to new individual thallus. Before dark treatment, the <i>U.</i> <i>prolifera</i> cells were filled with plastid, contained visible starch grain and discernible cell outlines, while after 120 days of dark treatment, the plastid shrank and degraded together with the disappearance of cell inclusions, and the cell outlines also blurred, then those samples were transferred to optimal culture conditions at 20<span style="white-space:nowrap;">°</span>C in 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> light intensity, and 15 days later, newly-grown cells appeared on the almost dead thallus, these cells divided continuously and grew to young thallus, and those newly-grown thallus also generated active germ cells, which developed to new thallus that cytologically identical to the original thallus. Observation of chopped tissue of <i>U.</i> <i>prolifera</i> cultivated at 20<span style="white-space:nowrap;">°</span>C, 40</span></span><span style="white-space:normal;"><span style="font-family:;" "=""> </span></span><span style="white-space:normal;"><span style="font-family:;" "="">μmol m</span></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">-</span></sup></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">2</span></sup></span><span style="white-space:normal;"><span style="font-family:;" "="">·s</span></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">-</span></sup></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">1</span></sup></span><span style="white-space:normal;"><span style="font-family:;" "=""> showed that the morphological upper part cells turned to germ cells first, those germ cells including gametophyte and sporophyte, which released later and grew to new individual thallus. These findings provided cytological evidences for how <i>U. prolifera</i> live through stress conditions such as low temperature, darkness, and also useful for understanding the mechanism of the occurrence of green tide.</span></span>展开更多
基金Supported by National Algae System(CARS-50)Modern Agricultural(Laver)Industrial Technology System of Jiangsu Province(JATS[2023]381)Research Project of Nantong City(MS22022065).
文摘[Objectives]To study the differences of growth rate,morphology,ultrastructure,pigment content and antioxidant enzyme activity of free-living conchocelis of cultivated type of Neopyropia yezoensis under different light qualities(white,red,blue,and green light).[Methods]The study was carried out through light quality design and culture,growth rate determination,microstructure and ultrastructure observation,chlorophyll a content and carotenoid content determination,phycobiliprotein content determination,malondialdehyde(MDA)content determination,superoxide dismutase(SOD)activity determination.[Results]After 21 d of culture,the specific growth rate(SGR)and chlorophyll a content of free-living conchocelis of N.yezoensis were significantly increased by white light(WL),followed by red light(RL)and green light(GL),and they were the lowest under blue light(BL).Compared with the WL group,the BL group had the highest content of phycoerythrin(PE),and the RL and GL groups had the highest content of phycocyanin(PC).The algal body of WL group was normal black brown,and the cell wall was the thickest.In RL and GL groups,the algal bodies were green,and their diameters and cell wall thicknesses were similar to those in WL group.In BL group,the algal body was bright red,the diameter was the smallest,the cell wall was the thinnest,and the ultrastructure showed that the number of plastoglobulus on the thylakoid was the largest.After BL irradiation,the highest MDA content and the lowest SOD activity were observed.The results revealed that WL is the most beneficial to the growth of free-living conchocelis,followed by RL and GL,while BL has adverse effects.[Conclusions]This study explored the most suitable light quality conditions for the propagation of free-living conchocelis.It is expected to provide germplasm guarantee for the production and seedling of N.yezoensis.
文摘The cytological characteristics of major green-tide-forming green algae <i>Ulva prolifera</i> collected from Yellow Sea were studied th<span style="white-space:normal;"><span style="font-family:;" "="">r</span></span><span style="white-space:normal;"><span style="font-family:;" "="">ough cutting segments, long time low temperature or dark treatments. After </span></span><span style="white-space:normal;"><span style="font-family:;" "="">being </span></span><span style="white-space:normal;"><span style="font-family:;" "="">dried in the shade and preserved at -</span></span><span style="white-space:normal;"><span style="font-family:;" "="">20<span style="white-space:nowrap;">°</span></span></span><span style="white-space:normal;"><span style="font-family:;" "="">C for 30 days, the <i>U.</i> <i>prolifera</i> was cultured at 4<span style="white-space:nowrap;">°</span>C in sterilized seawater under 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> light intensity for 120 days, results indicated that the plastid of <i>U. prolifera</i> continuously shrank with the extension of treatment, and most cells turned white and died, only a small amount of cells still contained a few of visible inclusions at the 120d of treatment. Then those samples were transferred to 20<span style="white-space:nowrap;">°</span>C and 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> condition for recovery cultivation, after about 10 days, some recovery cells were observed in the thallus, and those cells developed to young thallus gradually and released germ cells almost in the same time. After about 60 days of recovery cultivation, the newly-grown green thallus broke through the original dead thallus, and the germ cells also grew to new individual thallus. Before dark treatment, the <i>U.</i> <i>prolifera</i> cells were filled with plastid, contained visible starch grain and discernible cell outlines, while after 120 days of dark treatment, the plastid shrank and degraded together with the disappearance of cell inclusions, and the cell outlines also blurred, then those samples were transferred to optimal culture conditions at 20<span style="white-space:nowrap;">°</span>C in 40 μmol photons m<sup>-2</sup>·s<sup>-1</sup> light intensity, and 15 days later, newly-grown cells appeared on the almost dead thallus, these cells divided continuously and grew to young thallus, and those newly-grown thallus also generated active germ cells, which developed to new thallus that cytologically identical to the original thallus. Observation of chopped tissue of <i>U.</i> <i>prolifera</i> cultivated at 20<span style="white-space:nowrap;">°</span>C, 40</span></span><span style="white-space:normal;"><span style="font-family:;" "=""> </span></span><span style="white-space:normal;"><span style="font-family:;" "="">μmol m</span></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">-</span></sup></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">2</span></sup></span><span style="white-space:normal;"><span style="font-family:;" "="">·s</span></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">-</span></sup></span><span style="white-space:normal;"><sup><span style="font-family:;" "="">1</span></sup></span><span style="white-space:normal;"><span style="font-family:;" "=""> showed that the morphological upper part cells turned to germ cells first, those germ cells including gametophyte and sporophyte, which released later and grew to new individual thallus. These findings provided cytological evidences for how <i>U. prolifera</i> live through stress conditions such as low temperature, darkness, and also useful for understanding the mechanism of the occurrence of green tide.</span></span>