文心兰高效再生体系的建立

[目的]建立文心兰高效再生体系,为利用转基因技术进行品种改良提供科学依据.[方法]以文心兰柠檬绿的无菌苗叶片为材料,探讨不同植物生长调节剂配比对其原球茎诱导的影响,开展增殖、生根及移栽研究,建立其高效稳定的再生体系.[结果]影响文心兰原球茎诱导的3种植物生长调节剂主次排序为萘乙酸(NAA)>噻苯隆(TDZ)>6-苄氨基嘌呤(6-BA),在1/2MS培养基中添加0.5 mg/L NAA、0.5 mg/L 6-BA和0.3 mg/L TDZ的诱导率最高,达48.0%.培养基中活性炭含量及碳水化合物种类对文心兰原球茎增殖的影响存在明显差异,不同活性炭含量处理间的原球茎增殖系数存在显著差异(P<0.05,下同),添加1.0 g/L活性炭较添加0.5 g/L活性炭的增殖系数显著升高,不同碳水化合物种类间的原球茎增殖系数排序为海藻糖>麦芽糖>蔗糖,最佳增殖和分化培养基为1/2MS+4.0 mg/L 6-BA+0.4 mg/L NAA+1.0 g/L活性炭+20 g/L海藻糖.添加10%椰子水的文心兰幼苗生根数显著高于添加10%香蕉汁和10%苹果汁,每株平均生根量接近4.00条,即生根效果最佳的培养基为1/2MS+0.8 mg/L 6-BA+0.2 mg/L NAA+10%椰子水.移栽过程中根部用水苔包裹后再移至椰糠中,保证光照、水分适宜,适当添加缓释肥,移栽成活率可达100%.[结论]利用海藻糖或麦芽糖作为碳源的文心兰原球茎增殖效果较优,生根数和生根质量优势明显;不同植物生长调节剂配比、碳源和有机物的添加对文心兰组织培养具有明显的促进效果.     

小黑麦不同品种劣变种子的胚培养效果研究

试验选用从澳大利亚引进的10个小黑麦品种的劣变种子的胚在1/2MS+2%蔗糖+0.1%麦芽糖+0.5%琼脂、pH 5.8的培养基中进行培养。结果表明:劣变小黑麦品种种子胚的发育率和成苗率由高到低分别为:DH265Cherokee2090WhiteAT528WhileM96-3182-1AT754AT315和CherokeeDH2652090WhiteAT528WhileM 96-3182-1AT754AT315,试验材料的胚发育率和成苗率均显著低于正常小黑麦材料(CK1,CK2);小黑麦品种33rd ITSN,32rd ITSN和Rhino的胚发育率和成苗率均为0;劣变小黑麦种子进行胚培养时,诱导培养的适宜时间为27d。     

2种低毒杀虫剂防治水稻粘虫示范试验

为合理使用低毒农药防治水稻粘虫,2015年7月在广西乐业县同乐镇和甘田镇进行25%灭幼脲悬浮剂和2.2%甲氨基阿维菌素苯甲酸盐微乳剂防治粘虫大田示范试验。结果表明:施药后17 d,核心区25%灭幼脲对粘虫的防治效果和保叶率分别为96.19%和94.73%,在培训指导农民防治示范区的防效分别为93.50%和95.10%;施药后10 d,核心区2.2%甲氨基阿维菌素苯甲酸盐对粘虫的防治效果和保叶率分别为96.61%和97.35%,在培训指导农民防治示范区的防效分别为90.07%和89.59%。25%灭幼脲和2.2%甲氨基阿维菌素苯甲酸盐处理区对粘虫的防效均要高于农民自防区。     

政府渔业补助政策与博弈

渔业补助政策是政府为弥补市场经济缺陷而采取的重要措施，本文应用博弈论对政府与渔民的互动博弈展开研究，并确立了混合策略模型下的政府和渔民各自最佳选择概率，达到纳什均衡，这对于解释当前政府渔业补助政策内涵与指导修订补助政策有参考意义。     

马传贫驴白细胞弱毒疫苗株跨膜蛋白主要免疫决定区基因的克隆与表达

从感染驴白细胞的马传贫驴白细胞弱毒疫苗株前病毒DNA中克隆了编码跨膜蛋白主要免疫决定区(TMIR)的基因，并在大肠杆菌中进行了表达。所表达的融合蛋白有一部分是可溶的，其氨基端带有6个组氨酸的标签，因此可以用固定化金属离子亲和层析法在非变性条件下进行纯化。在间接酶联免疫吸附试验(ELISA)和免疫印迹试验中，重组的TMIR蛋白可与马传贫阳性血清样品发生反应，而与健康马血清无任何反应。这表明该重组蛋白具有良好的抗原性和特异性，可用于马传贫弱毒疫苗株在体内外复制、接种马体内免疫应答及马传贫诊断的研究。     

Development of Chinese Near-isogenic Line of Rice and Their Differentiating Ability of Pathogenic Races of Blast Fungus

The rice( Oryza L. ) variety, Lijiangxintuanheigu(LTH), is a universally susceptible variety. A set of near-isogenic lines (NILs) of rice which has single resistance gene for each line was developed by use of LTH as recurrent parent and Kusabue,Tsuyuake, K1, PiNo. 4, K60 and BL1, which are from Kiyosawa‘s differential varieties(KDV), as donor parents. Differentiating ability of these NILs to Philippine isolates was compared with that of their donor parents, KDV and IRRI‘ s NILs. The results of comparative studies were as follows: (1) Differentiating ability of Chinese NILs to Philippine isolates was much stronger than that of their donor parents and that of KDV. (2) Chinese NILs had similar ability to differentiate races to IRRI‘s NILs or higher differentiating ability than them. But IRRI‘s NILs almost had no differentiating ability to isolates from japonica rice-growing regions. They can not be used to differentiate races of isolates from japonica ricegrowing regions. Whereas, Chinese NILs can be used to differentiate races of isolates from both japonica ricegrowing regions and indica rice-growing regions. It was concluded that the set of Chinese NILs can be used as international differentials.     

法氏囊活性肽对鸡体增重及饲料转化率的影响

把不同剂量的法氏囊活性肽 (BS)冻干粉与传染性法氏囊病 (IBD)活苗混合后 ,对 2 1日龄SPF鸡滴鼻点眼 ,同时另选一批同样生长状态的鸡 ,在颈部皮下接种IBD细胞毒油苗 ,同时肌肉注射上述不同剂量法氏囊活性肽 ,观察法氏囊活性肽对鸡生长性能的影响。结果发现 :免疫后7d ,活苗 0 2mLBS组增长最快 ,比免疫对照组多增 82 5 % ,并且饲料报酬高。但从整个试验期看 ,0 4mLBS组增重效果较好 ,比免疫对照组多增 1 9 8% ,并且有较高的饲料转化率。而肌肉注射BS组中 ,高剂量 (0 8mL)BS组的增重效果一直很好 ,比对照组总增重平均多增 7 2 3 % ,并有较高的饲料报酬。这说明滴鼻点眼或是肌肉注射 ,BS都有促生长的作用     

脂肪细胞培养研究现状

脂肪细胞培养为研究脂肪代谢紊乱疾病提供了一种有效的途径。基质血管成分系统的研究形成了完整的前脂肪细胞理论,随后脂肪细胞原代培养技术得到了广泛的研究,国外各种家畜的脂肪细胞培养模型得以建立,而国内在脂肪细胞培养方面的研究起步较晚,且多集中于人及鼠的脂肪细胞培养。脂肪细胞的传代培养在单一因子对脂肪细胞的功能研究上有一定的优越性,尤其对不宜于在活体采样的人及动物。脂肪细胞培养的另一个研究方向是脂肪细胞与其他组织细胞的联合培养,对研究机体内各种组织细胞间的相互作用提供了良好的基础。     

Effects of oxidized low density lipoprotein and lysophosphatidylcholine on cholesterol efflux from mouse peritoneal macrophage foam cells

AIM:To explore the effects of oxidized low density lipoprotein (OxLDL) and one of its component— lysophosphatidylcholine (LPC) on cholesterol efflux from mouse macrophage foam cells.METHODS:(1) Cholesterol efflux induced by apoAI from mouse peritoneal macrophage foam cells loaded with OxLDL or acylated LDL(AcLDL) was measured. (2) Cholesterol efflux induced by LPC and apoAI from macrophage foam cells separated from normal or apoE gene deficient (E⁰) mouse loaded with AcLDL were measured.RESULTS:(1) When the macrophage foam cells were incubated with apoAI, cholesterol efflux from AcLDL-induced macrophage foam cells increased significantly compared to that of OxLDL-induced macrophage foam cells. (2) LPC promoted cholesterol efflux from macrophage foam cells in relation to both dosage and time. When LPC was incubated with E⁰ mouse macrophage foam cells, the released cholesterol mass was significantly lower than that of normal mouse macrophage foam cells. It was also found that cholesterol efflux induced by apoAI normally occurred in E⁰ mouse macrophage foam cells.CONCLUSIONS:(1) OxLDL accumulated cholesterol in macrophages and impair cholesterol efflux. (2) LPC induced cholesterol efflux from macrophage foam cells, which may occur via apoE pathway.     

Effect of antifibrotic herb serum on rat hepatic stellate cell proliferation and collagen synthesis

AIM: To investigate the effect of Chinese herbs, Ganxianfang(GXF), on rat hepatic stellate cells (HSC) proliferation and collagen synthesis. METHODS: Two types of herb serum, portal venous serum and circumferential venous serum, were prepared from rats infused intragastrically with 16, 8, 4 times adult dose of GXF decoction. HSC isolated from rat liver were processed with the above sera in vitro. Then we mensurated the radioactivity of HSC admixed with [[³H]H]proline and [[³H]H]thymine to judge the effect on proliferation and collagen synthesis of HSC. RESULTS: Both two types of serum collected 0.5, 1, 2 h after intragastrical infusion inhibited HSC proliferation (P＜0.05), and the serum collected 1 h after intragastrical infusion had the strongest effect (P＜0.05). Portal serum decreasea collagen synthesis (P＜0.05), but circumferential serum had no effect (P＞0.05). CONCLUSION: Inhibition of HSC proliferation and decrease of collagen synthesis may contribute to the GXF antifibrotic action.