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以文心兰侧芽为外植体,研究侧芽采前处理、消毒次数、培养基中不同椰子汁含量配比对丛生芽诱导的影响。结果表明,采用在培养基中添加天然植物体,以幼嫩的椰子汁本身所含的微量激素和植物细胞分裂所需的关键诱导因子代替人工合成激素,对以文心兰侧芽为外植体进行丛生芽的诱导效果明显;以文心兰侧芽为外植体,通过采前5~7 d对植株的控水和喷施抗菌剂相结合的方法处理后,可避免病菌感染;经过连续2次0.15% 的升汞溶液灭菌(其中消毒时间为第1次7~8 min,第2次30~50 s),消毒效果最好;以(1/3大量元素)MS+15 相似文献
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以文心兰的侧芽为外植体,对侧芽的选择、处理,外植体的消毒方法、培养基的选择等技术进行研究。结果表明:最适合的材料为叶片还未展开的侧芽,二次消毒对文心兰侧芽消毒效果最好。文心兰理想的诱导培养基为MS+6-BA 5.0 mg/L+NAA 0.5 mg/L+椰子水100 mL/L,增殖培养基为MS+6-BA 2.0 mg/L+NAA 0.2mg/L+椰子水100 mL/L,壮苗培养基为MS+香蕉20g/L,生根培养基为1/2MS+NAA 1.0 mg/L+香蕉50 g+土豆20 g/L+AC2.0 g/L。同时 相似文献
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采用单因素随机区组试验方案探究降香种子玻璃化超低温保存最适条件,结合显微切片观察和生理生化特性检测对冷冻后细胞形态和生理生化指标变化进行分析,同时运用形态观察法和相关序列扩增多态性(SRAP)分子标记法对超低温保存后的降香植株遗传稳定性进行检测。结果表明:降香种子玻璃化超低温保存最佳条件为:室温(25 ℃)装载 25 min,0 ℃ 玻璃化脱水 30 min,40 ℃水浴解冻 5 min。对比检测不同冷冻时间的降香种子超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、α-淀粉酶、脱氢酶活性、丙二醛(MDA)含量以及电导率等生理生化指标,无明显差异。显微观察超低温保存前后的降香种胚内部结构,未见明显变化。超低温保存后的降香种子发芽时,出现短暂的生长停滞期,恢复培养后,其表观形态指标与对照植株无明显差异。SRAP技术分析了超低温冷冻前后的降香再生植株,其 SRAP 带型基本一致,未见明显差异带型。综上表明,超低温保存降香种子是长期稳定、安全可靠的。 相似文献
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对华贵栉孔扇贝(Chlamys nobilis)注射不同密度的溶藻弧菌(Vibrio alginolyticus),于注射后6,12,18,48,72h测定体内过氧化氢酶(CAT)、超氧化物岐化酶(SOD)、碱性磷酸酶(ALP)和酸性磷酸酶(ACP)的活力。结果表明:5×107cell.mL-1,5×108cell.mL-1组血淋巴中CAT活性均有升高趋势,其中5×108cell.mL-1组在18h极显著增加(P≤0.01),24h显著增加(P≤0.05)。5×108cell.mL-1组SOD活性最初表现为抑制,在12h和18h显著低于对照组(P≤0.05),24h后明显升高,5×107cell.mL-1组与对照组相比差异不明显。肝脏中ALP活性在18h与对照组相比,5×108cell.mL-1组极显著升高(P≤0.01),5×107cell.mL-1组显著升高(P≤0.05)。注射后ACP活性有明显升高的趋势,5×108cell.mL-1组在12h和18h显著高于对照组(P≤0.05),且在注射后24h5×107cell.mL-1,5×108cell.mL-1组活性均达到最高。 相似文献
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以文心兰南茜品种为原材料,筛选出自然变异优良单株博大1号,经组培扩繁获得新种苗,通过品种对比试验,对选育的新品种进行性状鉴定;再以引进的其他6个不同来源(品种)的文心兰产品为对照,在大田生产统一管理下,对植株生长、开花特性、切花等级、病虫害等进行比较。结果表明:7种材料中,博大1号整体综合性状优良,植株长势较为粗壮,全年感病率最低,仅3.4%,当年开花率最高,达81.96%,且具有较高的切花等级;切花后从新芽露出到花朵开放需要时间最短,仅175.1 d,切花株抽芽数最多,双芽以上株比例达92.5%,具有最高产的潜力。 相似文献
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AIM: To investigate the protective role of heat-shock protein 70 (HSP70) in the pathogenesis of gastric mucosal damage in cirrhotic rats with portal hypertensive gastropathy (PHG).METHODS: The rat model of liver cirrhosis with PHG was established by injection with tetrachloride.The animals were divided into normal control group, PHG group, PHG+heat treatment group, PHG+BPI21 group and PHG+endotoxin groups.The endotoxin used in the experiment was at the dose of 3 mg/kg and endotoxin antagonist BPI21 was at the dose of 2 mg/kg.HSP70 was induced by pre-treating the animals with mild whole-body heating.The levels of HSP70 and tumor necrosis factor alpha (TNF-α) in the gastric mucosa were measured by ELISA.Furthermore, the pathological changes of the gastric mucosa were observed under microscope with HE staining.RESULTS: Compared with the normal control rats, the rats in PHG group showed obvious gastric pathological lesion, decrease in HSP70 production and increase in TNF-α level in the gastric mucosa, and increased endotoxin concentration in the plasma.Compared with PHG+endotoxin group, the gastric mucosal lesion in PHG+BPI21 group was significantly attenuated, accompanied by the increase in HSP70 production and decrease in TNF-α level in the gastric mucosa.Heat treatment increased HSP70 production and decreased TNF-α concentration in the PHG rats, thus attenuating the gastric mucosal damage.CONCLUSION: HSP70 alleviates the gastric mucosal lesion induced by endotoxin in cirrhotic rats with PHG and decreases the concentration of TNF-α in gastric mucosa, indicating a protective role of HSP70 in the pathogenesis of gastric mucosal damage in PHG. 相似文献