The changes in arachidonic acid (AA) and fatty acids profiles along the growth curve of Parietochloris incisa, a coccoid snow green alga, were studied in a 2.8 cm light-path flat photobioreactor, exposed to strong pho...The changes in arachidonic acid (AA) and fatty acids profiles along the growth curve of Parietochloris incisa, a coccoid snow green alga, were studied in a 2.8 cm light-path flat photobioreactor, exposed to strong photon flux density [PFD, 2400 μEmol/(m 2·s)]. Sixteen fatty acids were identified by gas chromatography showing that AA was the dominant fatty acid (33%-41%) followed by linoleic acid (17%-21%). AA content was closely investigated with respect to total fatty acids (TFA), ash free dry weight (AFDW) of cell mass as well as total culture content. These parameters were influenced significantly in a similar manner by culture growth phase, i.e., slightly decreasing in the lag period, gradually increasing in the logarithmic phase, becoming maximal at the early stationary phase, starting to decrease at the late stationary phase, sharply dropping at the decline phase. The increase in AA per culture volume during the logarithmic phase was not only associated with the increase in AFDW but also connected with a corresponding increase in AA/TFA, TFA/AFDW as well as AA/AFDW. The sharp decrease in AA content of the culture during the decline phase was mainly due to the decrease in AA/TFA, TFA/AFDW and AA/AFDW, although AFDW declined only a small extent. Maximal AA concentration, obtained at the early stationary phase, was 900 mg/L culture volume, and the average daily net increase of AA during 9 days logarithmic growth was 1.7 g/(m 2·day). Therefore, harvesting prior to the decline phase in a batch culture, or at steady state in continuous culture mode seems best for high AA production. The latter possibility was also further confirmed by continuous culture with 5 gradients of harvesting rate.展开更多
Objective: To observe the oxidative modification of high density lipoprotein (HDL) induced by cultured human arterial smooth muscle cells (SMCs). Methods: HDL cocultured with SMCs at 37℃ in 48 h was subjected, and na...Objective: To observe the oxidative modification of high density lipoprotein (HDL) induced by cultured human arterial smooth muscle cells (SMCs). Methods: HDL cocultured with SMCs at 37℃ in 48 h was subjected, and native HDL (N-HDL) served as control. Oxidative modification of HDL was identified by using agarose gel electrophoresis. Absorbances of conjugated diene (CD) and lipid hydroperoxide (LOOH) were measured with ultraviolet spectrophotometry at 234 and 560 nm respectively, and fluorescence intensity of thiobarbuturic acid reaction substance (TBARS) with fluorescence spectrophotometry at 550 nm emission wavelength with excitation at 515 nm. Results: In comparison with N-HDL, the electrophoretic mobility of SMCs-cocultured HDL was increased, and the contents of CD, LOOH and TBARS HDL were very significantly higher than those of the control HDL (P<0.01). Conclusion: Oxidative modification of HDL can be induced by human arterial SMCs.展开更多
The key limiting factors to high-density culture of Porphyridium cruentum are the uptake of light energy and nutrient by the microalgal cells. Under the optimal conditions of carrier culture, both cell mass and cell d...The key limiting factors to high-density culture of Porphyridium cruentum are the uptake of light energy and nutrient by the microalgal cells. Under the optimal conditions of carrier culture, both cell mass and cell density were increased significantly up to 5.2 g/L (DW) and 5.2107/ml. Furthermore, the effects of the liquid circulation velocity, light intensity and initial cell density on cell mass productivity of P. cruentum were investigated in a 42 L internal loop airlift photobioreactor. Although the light intensity was as low as 100 mmol/(m2s), the light damage or the photoinhibition phenomenon was observed under the culture condition of low initial cell mass (0.10 g/L, DW) and high liquid circulation velocity (0.30 m/s). However, a higher cell growth rate and a high cell mass productivity were achieved with the same conditions only at high initial cell mass (about 0.80 g/L, DW). Under the optimal conditions, the cell specific growth rate, cell mass volumetric and areal output rate reached to 0.95 d-1, 0.80 g/(Ld) and 42.5 g/(m2d) respectively. Finally, a method of nutrient feeding and gradual increase of light intensity in different cultural stages was developed, which further improved the cell mass, cell mass volumetric and areal output rate to 5.9 g/L, 1.2 g/(Ld) and 61.7 g/(m2d) respectively.展开更多
文摘The changes in arachidonic acid (AA) and fatty acids profiles along the growth curve of Parietochloris incisa, a coccoid snow green alga, were studied in a 2.8 cm light-path flat photobioreactor, exposed to strong photon flux density [PFD, 2400 μEmol/(m 2·s)]. Sixteen fatty acids were identified by gas chromatography showing that AA was the dominant fatty acid (33%-41%) followed by linoleic acid (17%-21%). AA content was closely investigated with respect to total fatty acids (TFA), ash free dry weight (AFDW) of cell mass as well as total culture content. These parameters were influenced significantly in a similar manner by culture growth phase, i.e., slightly decreasing in the lag period, gradually increasing in the logarithmic phase, becoming maximal at the early stationary phase, starting to decrease at the late stationary phase, sharply dropping at the decline phase. The increase in AA per culture volume during the logarithmic phase was not only associated with the increase in AFDW but also connected with a corresponding increase in AA/TFA, TFA/AFDW as well as AA/AFDW. The sharp decrease in AA content of the culture during the decline phase was mainly due to the decrease in AA/TFA, TFA/AFDW and AA/AFDW, although AFDW declined only a small extent. Maximal AA concentration, obtained at the early stationary phase, was 900 mg/L culture volume, and the average daily net increase of AA during 9 days logarithmic growth was 1.7 g/(m 2·day). Therefore, harvesting prior to the decline phase in a batch culture, or at steady state in continuous culture mode seems best for high AA production. The latter possibility was also further confirmed by continuous culture with 5 gradients of harvesting rate.
文摘Objective: To observe the oxidative modification of high density lipoprotein (HDL) induced by cultured human arterial smooth muscle cells (SMCs). Methods: HDL cocultured with SMCs at 37℃ in 48 h was subjected, and native HDL (N-HDL) served as control. Oxidative modification of HDL was identified by using agarose gel electrophoresis. Absorbances of conjugated diene (CD) and lipid hydroperoxide (LOOH) were measured with ultraviolet spectrophotometry at 234 and 560 nm respectively, and fluorescence intensity of thiobarbuturic acid reaction substance (TBARS) with fluorescence spectrophotometry at 550 nm emission wavelength with excitation at 515 nm. Results: In comparison with N-HDL, the electrophoretic mobility of SMCs-cocultured HDL was increased, and the contents of CD, LOOH and TBARS HDL were very significantly higher than those of the control HDL (P<0.01). Conclusion: Oxidative modification of HDL can be induced by human arterial SMCs.
基金Supported by the China Ministry of Science and Technology(No. 96-C02-04-05)
文摘The key limiting factors to high-density culture of Porphyridium cruentum are the uptake of light energy and nutrient by the microalgal cells. Under the optimal conditions of carrier culture, both cell mass and cell density were increased significantly up to 5.2 g/L (DW) and 5.2107/ml. Furthermore, the effects of the liquid circulation velocity, light intensity and initial cell density on cell mass productivity of P. cruentum were investigated in a 42 L internal loop airlift photobioreactor. Although the light intensity was as low as 100 mmol/(m2s), the light damage or the photoinhibition phenomenon was observed under the culture condition of low initial cell mass (0.10 g/L, DW) and high liquid circulation velocity (0.30 m/s). However, a higher cell growth rate and a high cell mass productivity were achieved with the same conditions only at high initial cell mass (about 0.80 g/L, DW). Under the optimal conditions, the cell specific growth rate, cell mass volumetric and areal output rate reached to 0.95 d-1, 0.80 g/(Ld) and 42.5 g/(m2d) respectively. Finally, a method of nutrient feeding and gradual increase of light intensity in different cultural stages was developed, which further improved the cell mass, cell mass volumetric and areal output rate to 5.9 g/L, 1.2 g/(Ld) and 61.7 g/(m2d) respectively.
