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Impact of Some Agronomic Practices on Paddy Field Soil Health Under Varied Ecological Conditions: II. Influence of Soil Temperature 被引量:1
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作者 A.SUBHANI HUANGCHANGYONG 《Pedosphere》 SCIE CAS CSCD 2001年第2期143-150,共8页
A 21-d incubation experiment was conducted under controlled laboratory conditions to study the effects of elevated temperatures (10, 25, and 40 ℃) on some microbiological and biochemical properties in flooded paddy s... A 21-d incubation experiment was conducted under controlled laboratory conditions to study the effects of elevated temperatures (10, 25, and 40 ℃) on some microbiological and biochemical properties in flooded paddy soil amended or unamended with urea at 100 μg N g-1 soil and/or insecticide (triazophos) at field rate (FR). Enhancements in temperature led to increase the electron transport system (ETS) / dehydrogenase activity and phospholipid contents of the soil, while soil organic matter phenol and protein contents decreased with increasing temperature with or without the addition of inputs. An increase of temperature from 10 ℃ to 25 or 40 ℃ enhanced the ETS activity 2 folds (on average for all soils), while the inclusion of N and insecticide increased and decreased it, respectively, compared to the control. The soil phenol and protein contents were highly correlated with temperatures (for all soils, r = -0.936 and -0.971, respectively) and the additions of N and insecticide produced slight reductions and enhancements in them, respectively. At a particular temperature, the soil protein contents remained unaffected among all the soil treatments. An overall slight increase in phospholipid contents with N and a small decline with insecticide addition were noticed against the untreated soil. The toxicity of fertilizer and insecticide decreased as the incubation temperature increased, suggesting faster degradation of agrochemicals with raising temperature. 展开更多
关键词 electron transport system (ETS) activity PHENOL PHOSPHOLIPIDS PROTEIN temperature
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Purification and Antioxidant Activities of Phycocyanin from Spirulina Platensis
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作者 Pimporn Leelapompisid Watcharaporn Khamrat Dummrong Santiarworn 《Journal of Chemistry and Chemical Engineering》 2010年第7期12-16,共5页
This study aimed to purify and determine antioxidant activities of different fractions obtained during the purification process of phycocyanin from Spirulina platensis. The dried powder of Spirulina platensis, after g... This study aimed to purify and determine antioxidant activities of different fractions obtained during the purification process of phycocyanin from Spirulina platensis. The dried powder of Spirulina platensis, after ground with sands, was extracted with 50 mM sodium phosphate buffer at pH 6.8 before centrifuged to precipitate unwanted proteins. Then the supernatant was separated by celit column to obtain semi-pure phycocyanin and further purified by treated with ammonium sulfate. The purity of phycocyanin was monitored by measuring the absorbance spectrum from 200 to 700 nm. Its purity ratio A620A280 was determined. The antioxidant activities of the obtained phycocyanin were determined by 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) assay and lipid peroxidation (linoleie acid) assay. The purity ratio of phycocyanin in the Spirulina crude extract was 0.36 and increased to 2.68 after purification. The fraction with the highest purity ratio of phycocyanin demonstrated the hightest antioxidant activities. For ABTS assay, it presented the Vitamin C Equivalent Antioxidant Capacity (VCEAC) value of 0.0405 ±0.0002 mg of ascorbic acid/mg of sample and the Trolox Equivalent Antioxidant Capacity (TEAC) value of 0.0485 ±0.0002 mg oftrolox/mg of sample respectively. The result from lipid peroxidation assay exhibited IC50 value of 5.9336 ±0.2565 mg/mL. The purification of Spirulinaplatensis crude extract obtained from this study increased the purity ratio of phycocyanin and its antioxidant activities. This will be further investigated for the development into anti-aging cosmetic products. 展开更多
关键词 Spirulina platensis PHYCOCYANIN antioxidant activities.
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阿霉素诱导HK-2细胞损伤机制的研究 被引量:2
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作者 汤文洁 刘文超 高峰 《毒理学杂志》 CAS CSCD 北大核心 2016年第4期299-301,共3页
目的探讨阿霉素诱导人肾近端小管上皮细胞(HK-2 cells)损伤作用机制。方法用刃天青试验法检测阿霉素0-100μmol/L暴露HK-2细胞24 h对细胞存活率的影响,并计算半数致死浓度(LC50);检测细胞培养上清中乳酸脱氢酶(LDH)含量以及细胞内... 目的探讨阿霉素诱导人肾近端小管上皮细胞(HK-2 cells)损伤作用机制。方法用刃天青试验法检测阿霉素0-100μmol/L暴露HK-2细胞24 h对细胞存活率的影响,并计算半数致死浓度(LC50);检测细胞培养上清中乳酸脱氢酶(LDH)含量以及细胞内Caspase-3/7蛋白活性的变化;用荧光显微镜观察细胞内磷脂质蓄积情况。结果阿霉素暴露HK-2细胞24 h,可明显抑制HK-2细胞存活,且具有浓度依赖性(LC50=2.01±0.16μmol/L);阿霉素可以引起HK-2细胞培养上清中LDH含量显著升高(P〈0.01),细胞内Caspase-3/7蛋白活性显著升高(P〈0.01),且细胞存活率与胞外LDH含量及胞内Caspase-3/7蛋白活性均呈现明显的负相关性(r^2=0.986和r^2=0.991),LDH含量与Caspase-3/7蛋白活性呈现明显正相关性(r^2=0.999);荧光标记染色法观察到明显的细胞内磷脂质蓄积。结论阿霉素可诱导磷脂质在HK-2细胞内大量蓄积,导致细胞膜受损和细胞功能障碍,以及引发细胞凋亡,产生细胞毒性。 展开更多
关键词 阿霉素 HK-2细胞 磷脂质化 细胞毒性
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