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不同硝酸钾浓度对蔷薇藻生长及生理特性的影响 总被引:2,自引:0,他引:2
蔷薇藻(Rhodella reticulata)是属于红藻门的一种海洋单细胞微藻,其生长过程中产生藻胆蛋白、胞外多糖等生物活性物质.研究了不同硝酸钾浓度对蔷薇藻生长代谢的影响,分析测定蔷薇藻比生长速率、胞外多糖产量、藻蓝蛋白含量、色素含量、硝酸还原酶活性和SOD活性等参数.结果表明,与无氮培养基相比,蔷薇藻在以硝酸钾为氮源,浓度为0.75 g/L的条件下生长最好,硝酸还原酶活性最大,分别得到最大的藻蓝蛋白产量(24 mg/L)和类胡萝卜素含量(1.42 mg/L);当KNO3浓度为7.5 g/L时,获得最高叶绿素a含量为1.91 mg/L;高氮源有利于产糖,当KNO3浓度为30 g/L时,得到最高胞外多糖产量为1.633 g/L;SOD活性随硝酸钾浓度增加而增大. 相似文献
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蔷薇藻Rhodella reticulata是属于红藻门的一种海洋单细胞微藻,其生长过程中产生藻胆蛋白、胞外多糖等生物活性物质。蔷薇藻经过破碎,通过硫酸铵沉淀和DEAE Sepharose FF柱层析后,可以分离出较纯的藻蓝蛋白。本文从pH、温度、光照、食品添加剂、金属离子等方面对蔷薇藻藻蓝蛋白稳定性作了较全面的研究:藻蓝蛋白在pH为7时最稳定;低温有利于保持藻蓝蛋白的活性;相对于光照,在避光条件下,藻蓝蛋白有较高的稳定性;适当浓度的蔗糖和葡萄糖都有利于藻蓝蛋白的保存;金属离子影响藻蓝蛋白的稳定性。 相似文献
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响应面法优化螺旋藻藻蓝蛋白的超声波提取工艺 总被引:1,自引:0,他引:1
利用超声波破壁技术提取螺旋藻中的藻蓝蛋白,采用响应曲面法对工艺条件进行优化,模型决定系数(R2=99.95%)表明模型的拟合性好,得到的最佳工艺条件为:液料比为21 mL/g,超声波功率为640W,超声时间为14min。此条件下藻蓝蛋白的得率为10.76%,与模型预测值10.77%相近。对超声波提取法、冻融法、恒温浸提法进行比较研究,藻蓝蛋白的得率分别为10.76%、7.89%、6.57%,得知超声波提取法用时短、藻蓝蛋白得率高。 相似文献
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微鞘藻胞外多糖在沙漠土壤成土中的作用 总被引:27,自引:4,他引:23
研究了沙坡头藻结皮中的优势物种——微鞘藻的胞外多糖对沙漠表层土壤水分分布状况的影响及其光合特性。随着胞外多糖浓度的升高 ,土壤持水量增大 ,土壤水分蒸发速率降低 ,水分在土壤中运动的速率被延缓。藻总水溶性多糖产率为 2 8.82 % ,胞外水溶性多糖产率为 1 6 .0 9% ;多糖产量在稳定期生物量最大时增长最快。微鞘藻光合作用最适温度为 2 5℃ ,最适光强为 40 0 μE.m- 2 .s- 1,在 0 .3 mol/ L Na Cl浓度下其光合作用活性被强烈抑制 ;微鞘藻的吸收光谱表明它比生长在湿润地区的藻类含有更多的胡萝卜素成分 ;叶绿素 a荧光 (Fv/ Fm)分析表明在失水约为初始湿重的 5 6 %时 Fv/ Fm值恢复到水培养的 96 % ;其光合作用特性有利于对逆境的适应和生物量的积累。表明微鞘藻胞外多糖可影响沙漠表层土壤水分分布状况 ,并可作为一种潜在的生物肥料 ,在荒漠原始成土过程中扮演着重要角色。 相似文献
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水分对具鞘微鞘藻构建人工藻结皮的作用 总被引:3,自引:0,他引:3
为探讨水分在利用室内培养具鞘微鞘藻构建人工藻结皮中的作用,本文研究了不同施水量和施水时间下人工藻结皮中的藻类生物量、结皮厚度、抗压强度和微结构变化.结果表明:利用具鞘微鞘藻在裸沙上接种,无水处理藻类生物量极低,无藻结皮形成.随着施水量的增加,藻结皮开始出现直至形成稳定的藻结皮,藻类生物量、结皮厚度和抗压强度显著增加,藻丝和胞外多糖逐渐增多,与沙粒缠绕成复杂的网状结构.施水15 d,形成稳定的藻结皮,藻类生物量、结皮厚度和抗压强度最高.具鞘微鞘藻形成藻结皮的最适施水量是3~4L·m-2·d-1,施水时间为15 d.土壤可利用水分可促进具鞘微鞘藻的代谢活动和胞外多糖合成,从而增加藻类生物量,提高其耐旱能力,早期的水分获得是其成功形成藻结皮的关键因素.研究结果将为利用荒漠藻类进行人工生物结皮恢复提供重要的理论依据. 相似文献
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均匀设计法优化发菜细胞悬浮培养条件 总被引:2,自引:0,他引:2
通过摇瓶发酵实验研究了培养温度、光照强度等培养条件对发菜细胞悬浮培养生物量和代谢产物发菜多糖累积的影响,通过均匀设计试验对培养条件进行了优化。结果表明:在培养温度24℃、培养基初始pH8.0、光照强度60μmol/(m2.s)、转速150r/min的条件下培养20d,发菜细胞生物量(细胞质量浓度)达到1.34g/L,胞外多糖产量达到208.32mg/L;与优化前相比,发菜细胞生物量和胞外多糖产量分别提高27.3%、111.17%。 相似文献
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优化了爪哇曲壳藻亚缢变种(Achnanthes javanica var. subconstricta)胞外多聚物提取方法并分析了其化学组成。结果表明, 使用0.3 mol/L的碳酸氢钠提取时间为2.53h可充分提取非水溶性胞外多聚物而不会破碎细胞, 是最优的提取方法。爪哇曲壳藻亚缢变种胞外多聚物多糖占80%以上, 蛋白质占16%19%, 不含脂类。水溶性多糖的单糖组分摩尔比为: 岩藻糖:半乳糖:葡萄糖:甘露糖:木糖:鼠李糖=2.47:2.13:1:0.69:0.57:0.46,而非水溶性多糖的单糖组分摩尔比为: 半乳糖:岩藻糖:木糖:葡萄糖:甘露糖:鼠李糖=3.56:2.73:1.30:1:0.67:0.57。 相似文献
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In experiments on Black Sea skates (Raja clavata), the potential of the receptor epithelium of the ampullae of Lorenzini and spike activity of single nerve fibers connected to them were investigated during electrical and temperature stimulation. Usually the potential within the canal was between 0 and –2 mV, and the input resistance of the ampulla 250–400 k. Heating of the region of the receptor epithelium was accompanied by a negative wave of potential, an increase in input resistance, and inhibition of spike activity. With worsening of the animal's condition the transepithelial potential became positive (up to +10 mV) but the input resistance of the ampulla during stimulation with a positive current was nonlinear in some cases: a regenerative spike of positive polarity appeared in the channel. During heating, the spike response was sometimes reversed in sign. It is suggested that fluctuations of the transepithelial potential and spike responses to temperature stimulation reflect changes in the potential difference on the basal membrane of the receptor cells, which is described by a relationship of the Nernst's or Goldman's equation type.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. I. M. Sechenov, Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Pacific Institute of Oceanology, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 67–74, January–February, 1980. 相似文献
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N. P. Vesselkin Yu. V. Natochin 《Journal of Evolutionary Biochemistry and Physiology》2010,46(6):592-603
Evolution of living organisms is closely connected with evolution of structure of the system of regulations and its mechanisms.
The functional ground of regulations is chemical signalization. As early as in unicellular organisms there is a set of signal
mechanisms providing their life activity and orientation in space and time. Subsequent evolution of ways of chemical signalization
followed the way of development of delivery pathways of chemical signal and development of mechanisms of its regulation. The
mechanism of chemical regulation of the signal interaction is discussed by the example of the specialized system of transduction
of signal from neuron to neuron, of effect of hormone on the epithelial cell and modulation of this effect. These mechanisms
are considered as the most important ways of the fine and precise adaptation of chemical signalization underlying functioning
of physiological systems and organs of the living organism 相似文献
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