A simple instrument for the real-time measurement of algae concentration and mapping is described. The instrument uses a pulsed short arc xenon flashlamp as the excited light sources. Both the exciting light and the f...A simple instrument for the real-time measurement of algae concentration and mapping is described. The instrument uses a pulsed short arc xenon flashlamp as the excited light sources. Both the exciting light and the fluorescence from algae chlorophyll are transmitted along a fiber bundle. The measurement sensitivity is analyzed and the experiment result is given. The instrument is practical to in-situ measurement at sea.展开更多
We measured the concentrations of dimethylsulfide(DMS),acrylic acid(AA),and dimethylsulfoniopropionate(DMSP) during growth of three microalgae:Prorocentrum micans,Gephyrocapsa oceanica,and Platymonas subcordiformis.Th...We measured the concentrations of dimethylsulfide(DMS),acrylic acid(AA),and dimethylsulfoniopropionate(DMSP) during growth of three microalgae:Prorocentrum micans,Gephyrocapsa oceanica,and Platymonas subcordiformis.The DMSP,AA,and DMS concentrations in culture media varied significantly among algal growth stages,with the highest concentrations in the late stationary growth stage or the senescent stage.In the stationary growth stage,the average DMSP concentration per cell in P.micans(0.066 5 pmol/cell) was 1.3 times that in G.oceanica(0.049 5 pmol/cell) and 20.2 times that in P.subcordiformis(0.003 29 pmol/cell).The average concentrations of AA were0.044 6,0.026 9,and 0.003 05 pmol/cell in P.micans,G.oceanica,and P.subcordiformis,respectively,higher than the concentrations of DMS(0.272,0.497,and 0.086 2 fmol/cell,respectively).There were significant positive correlations between cell density and AA,DMSP,and DMS concentrations.The ratios of DMS/AA and AA/(DMSP+AA) in the three algae differed significantly over the growth cycle.In all three microalgae,the DMS/AA ratios were less than 25%during the growth period,suggesting that the enzymatic cleavage pathway,which generates DMS,was not the main DMSP degradation pathway.The changes in the DMS/AA ratio indicated that there was a higher rate of enzymatic breakdown of DMSP in the early growth period and a lower rate during senescence.In all three microalgae,the AA/(DMSP+AA) ratio(degradation ratio of DMSP) decreased during the exponential growth phase,and then increased.The variations in these ratios can approximately indicate the cleavage mechanism of DMSP at different stages of algal growth.展开更多
Inducing lipid accumulation in microalgae cells without suppressing cell growth is vital to the economical production ofbiodiesel from microalgae. In two experiments, we demonstrate that the eel1 concentration and lip...Inducing lipid accumulation in microalgae cells without suppressing cell growth is vital to the economical production ofbiodiesel from microalgae. In two experiments, we demonstrate that the eel1 concentration and lipid content of marine microalgae Isochrysis galbana depend upon the iron concentration in the growth media. In Experiment I, adding chelated FeC13 to the medium at the late exponential growth phase prolonged this phase and increased the lipid content in I. galbana cells. The final cell density and lipid content of I. galbana supplemented with chelated FeC13 was approximately 2 and 1.65 times higher than that of non-supplemented cultures, respectively. In Experiment II, I. galbana cells in the late exponential phase were collected and re-inoculated into new media containing Fe3+ at various concentrations. The final cell concentration and lipid content were maximized at the highest iron concentration (38% biomass by dry weight at 1.2×10^-5 mol/L Fe3+). In this study, intracellular neutral lipid storage was evaluated by fluorescent spectrophotometry using fluorochrome Nile red, and the measurement conditions were optimized.展开更多
In this study, we evaluated the anti-proliferative activity of phlorotannins derived from brown algae Laminariajaponica Aresch extracts on the human hepatocellular carcinoma cell (BEL-7402) and on routine leukemic c...In this study, we evaluated the anti-proliferative activity of phlorotannins derived from brown algae Laminariajaponica Aresch extracts on the human hepatocellular carcinoma cell (BEL-7402) and on routine leukemic cells (P388) by MTT assay. Cells were incubated with 100 μg/mL of the phlorotannin extract (PE) for 48 h. The inhibitory rate of PE on BEL-7402 and P388 cells was 30.20±1.16% and 43.44±1.86%, respectively, and the half-inhibitory concentration of PE (IC50) on P388 and BEL-7402 cells was 120 μg/mL and 〉200 μg/mL, respectively. Microscopic observation shows that the morphologic features of tumor cells treated with PE and 5-fluorouracil are markedly different from the normal control group. The inhibitory rate of fraction A2 isolated from PE by sephadex LH-20 for BEL-7402 and P388 cells at the sample concentration of 70.42 μg/mL was 61.96±7.02% and 40.47±8.70%, respectively. The apoptosis peak for fraction A2 was the most profound of all fractions used in the flow cytometry assay. The results indicate that the anti-proliferative of this algal extract is associated with the total phlorotannin content.展开更多
文摘A simple instrument for the real-time measurement of algae concentration and mapping is described. The instrument uses a pulsed short arc xenon flashlamp as the excited light sources. Both the exciting light and the fluorescence from algae chlorophyll are transmitted along a fiber bundle. The measurement sensitivity is analyzed and the experiment result is given. The instrument is practical to in-situ measurement at sea.
基金Supported by the National Natural Science Foundation of China(No.41176062)
文摘We measured the concentrations of dimethylsulfide(DMS),acrylic acid(AA),and dimethylsulfoniopropionate(DMSP) during growth of three microalgae:Prorocentrum micans,Gephyrocapsa oceanica,and Platymonas subcordiformis.The DMSP,AA,and DMS concentrations in culture media varied significantly among algal growth stages,with the highest concentrations in the late stationary growth stage or the senescent stage.In the stationary growth stage,the average DMSP concentration per cell in P.micans(0.066 5 pmol/cell) was 1.3 times that in G.oceanica(0.049 5 pmol/cell) and 20.2 times that in P.subcordiformis(0.003 29 pmol/cell).The average concentrations of AA were0.044 6,0.026 9,and 0.003 05 pmol/cell in P.micans,G.oceanica,and P.subcordiformis,respectively,higher than the concentrations of DMS(0.272,0.497,and 0.086 2 fmol/cell,respectively).There were significant positive correlations between cell density and AA,DMSP,and DMS concentrations.The ratios of DMS/AA and AA/(DMSP+AA) in the three algae differed significantly over the growth cycle.In all three microalgae,the DMS/AA ratios were less than 25%during the growth period,suggesting that the enzymatic cleavage pathway,which generates DMS,was not the main DMSP degradation pathway.The changes in the DMS/AA ratio indicated that there was a higher rate of enzymatic breakdown of DMSP in the early growth period and a lower rate during senescence.In all three microalgae,the AA/(DMSP+AA) ratio(degradation ratio of DMSP) decreased during the exponential growth phase,and then increased.The variations in these ratios can approximately indicate the cleavage mechanism of DMSP at different stages of algal growth.
基金Supported by the National Natural Science Foundation of China(No.40966002)the Natural Science Foundation of Hainan Province,China(No.409001)
文摘Inducing lipid accumulation in microalgae cells without suppressing cell growth is vital to the economical production ofbiodiesel from microalgae. In two experiments, we demonstrate that the eel1 concentration and lipid content of marine microalgae Isochrysis galbana depend upon the iron concentration in the growth media. In Experiment I, adding chelated FeC13 to the medium at the late exponential growth phase prolonged this phase and increased the lipid content in I. galbana cells. The final cell density and lipid content of I. galbana supplemented with chelated FeC13 was approximately 2 and 1.65 times higher than that of non-supplemented cultures, respectively. In Experiment II, I. galbana cells in the late exponential phase were collected and re-inoculated into new media containing Fe3+ at various concentrations. The final cell concentration and lipid content were maximized at the highest iron concentration (38% biomass by dry weight at 1.2×10^-5 mol/L Fe3+). In this study, intracellular neutral lipid storage was evaluated by fluorescent spectrophotometry using fluorochrome Nile red, and the measurement conditions were optimized.
基金Supported by the National Key Technology Research & Development Program of the 11th Five Year Plan of China (No. 2006BAD30B01)the National Natural Science Foundation of China (No. 30871945)
文摘In this study, we evaluated the anti-proliferative activity of phlorotannins derived from brown algae Laminariajaponica Aresch extracts on the human hepatocellular carcinoma cell (BEL-7402) and on routine leukemic cells (P388) by MTT assay. Cells were incubated with 100 μg/mL of the phlorotannin extract (PE) for 48 h. The inhibitory rate of PE on BEL-7402 and P388 cells was 30.20±1.16% and 43.44±1.86%, respectively, and the half-inhibitory concentration of PE (IC50) on P388 and BEL-7402 cells was 120 μg/mL and 〉200 μg/mL, respectively. Microscopic observation shows that the morphologic features of tumor cells treated with PE and 5-fluorouracil are markedly different from the normal control group. The inhibitory rate of fraction A2 isolated from PE by sephadex LH-20 for BEL-7402 and P388 cells at the sample concentration of 70.42 μg/mL was 61.96±7.02% and 40.47±8.70%, respectively. The apoptosis peak for fraction A2 was the most profound of all fractions used in the flow cytometry assay. The results indicate that the anti-proliferative of this algal extract is associated with the total phlorotannin content.