狗牙根与空心莲对水库消落带土壤氮磷释放影响的模拟

通过水库水位涨落室内模拟试验,探究丹江口库区消落带优势物种狗牙根和空心莲2种草本植物对土壤氮磷释放过程影响。结果表明:(1)水淹结束后(32天),空心莲子草土壤TN、TP分别降低11.75%,25.28%,狗牙根分别降低3.62%,25.77%。(2)干湿交替环境主要影响土壤中NH_4~+-N、NO_3~--N和AP的含量的变化,对土壤中的TN、TP含量的影响较小。(3)狗牙根的死亡增加土壤TN、NH_4~+-N、TP量,即不耐淹植被过滤带虽然能净化径流中N、P等污染物,但截留的污染物和植物吸收的养分随着植物体的分解再次进入水体或土壤,无法达到有效防控农业面源污染的目的。该研究为丹江口水库利用植被缓冲带防控水体富营养化提供一定理论依据。     

大型真菌重金属富集能力与机制研究进展

部分大型真菌有媲美甚至超过超累积植物的重金属富集能力,如蛹虫草(Cordyceps militaris)对Zn富集浓度可达20 000mg·kg-1以上,因而在污染环境的生态修复方面有着重要的应用前景。本文综述了近年报道的部分大型真菌的重金属富集能力,分析了不同生长时期、生长部位对重金属的富集特性,并对不同品种做了对比分析。大型真菌对自身重金属富集能力的调控有多种机制,包括胞外聚合物沉淀、细胞壁吸附和细胞内吸收,进入细胞的重金属可通过螯合、转运或引起氧化胁迫应激等途径来降低对细胞的毒害。基于大型真菌重金属富集能力强的优势,本文提出了拓展应用的方向及对目前存在问题的若干对策,从而为国内这一方向的发展提供参考。     

碱蓬根际和内生细菌菌株对盐碱胁迫下苜蓿生长的影响

为研究碱蓬根际和内生细菌菌株对盐碱胁迫下苜蓿幼苗生长的影响,试验以龙牧801紫花苜蓿为供试品种,将前期从碱蓬根内(JG1)、根际土壤(JT4)和茎内(JJ5)筛选出的具有较强耐盐碱胁迫能力的根际及内生细菌菌株接种于苜蓿幼苗根部。接菌1周后将中性盐(NaCl、Na₂SO₄)和碱性盐(NaHCO₃、Na₂CO₃)按NaCl∶Na₂SO₄∶NaHCO₃∶Na₂CO₃=9∶1∶1∶9混合,并设置0、100、150、200 mmol·L^-1盐碱浓度溶液浇灌苜蓿幼苗根部,进行盐碱胁迫处理。分析盐碱胁迫下碱蓬根际及内生细菌菌株对苜蓿生长及生理的影响,并通过隶属函数和主成分分析综合评价碱蓬根际和内生细菌菌株对盐碱胁迫下苜蓿生长的影响。结果表明:3株促生细菌均能缓解盐碱胁迫对紫花苜蓿生长的抑制作用,促进紫花苜蓿生长,不同促生细菌对盐碱胁迫下苜蓿促生效果为JT4>...     

无核白浓缩汁加工工艺

以无核白葡萄干为原料,对无核白浓缩汁的生产工艺进行研究,确定最佳的工艺条件。结果表明,料液比1∶3,复水温度50℃,复水时间4 h为无核白葡萄干最佳复水条件;酶解最佳工艺条件酶解时间60 min,pH值3,酶解温度40℃;旋转蒸发最佳条件温度80℃,浓缩无核白汁可溶性固形物为40 Brix。     

超微气泡增氧灌溉对水稻生育特性及产量的影响

以常规粳稻秀水09和杂交籼稻两优培九、国稻6号为试验材料,在2007和2008年采用大田试验,研究了超微气泡增氧灌溉对水稻生物学特性和产量的影响。结果表明,与常规灌溉相比,增氧灌溉处理具有分蘖发生快,叶面积指数大,干物质积累多等优点,尤其在生育后期表现出较大的干物质积累优势。增氧灌溉显著增加了水稻产量,其中秀水09分别增产8.45%(2007)和6.23%(2008)、国稻6号增产9.13%、两优培九增产7.49%。而且增氧灌溉明显提高了水稻有效穗数及结实率,但对水稻每穗总粒数和千粒重影响不明显。     

8种食用菌菌渣中3种饲用酶活性的测定

对可商业化人工栽培的8种常见食用菌菌渣中的木聚糖酶、β-葡聚糖酶和植酸酶生物活性进行了测定.结果表明,被测的8个样品均不同程度具有木聚糖酶和β-葡聚糖酶活性.其中,双孢蘑菇和毛木耳菌渣木聚糖酶活性最高,分别为2.856 U·g-1和1.109 U·g-1;杏鲍菇和毛木耳菌渣β-葡聚糖酶活性最高,分别为0.389 U·g-1和0.351 U·g-1;毛木耳在pH 2.5和pH 5.2下均具有植酸酶活性,分别为0.139 U·g-1和0.222 U·g-1;杏鲍菇和糙皮侧耳在pH 5.2下,植酸酶活性分别为0.126 U·g-1和0.122 U·g-1;其它菌渣均不具有明显的植酸酶活性.本研究表明,食用菌菌渣中具有一定的饲用酶活性,利用食用菌菌渣作为畜禽饲料,可在一定程度上减少饲用酶的添加,从而降低生产成本.     

Effect of 2, 3-butanedione monoxime (BDM) on myocardial protection in cold cardioplegia

AIM: The effects of BDM on isolated rat heart in cold cardioplegia were studied. METHODS: Rat heart were subjected to cold cardioplegia at 4℃ for 8, 18 and 24 h.Then each heart was perfused (90 cm H₂O) in Langendorff model at 37℃ for 40 min. In the high K⁺ group(n=24) the hearts were preserved in St.Thomas cardioplegic solution, in BDM group(n=24) hearts were preserved in K-H solution with BDM 30 mmoL/L. RESULTS: After 18 h, heart rate and the coronary flow in BDM group were significantly higher than in high K⁺ group(P＜0.05). Activity of Na⁺-K⁺-ATPase in cell membrane and in mitochondrial membrane in the BDM group was significantly higher than high K⁺ group(P＜0.01). After 24 h, all hearts in high K⁺ group were dead, but were alive in BDM group. CONCLUSION: Under given experiment conditions, BDM did enhance the tolerance to cold ischemia significantly. The results showed that BDM may become a useful agent for prolong the storage period of heart in cold cardioglegia.     

Protective effects of multi-enzyme Ⅱ on vascular endothelial cell injury induced by hyperlipidemia serum

AIM and METHODS: The protective effects of multi-enzyme Ⅱ was studied on cultured endothelial cells which was injuried by hyperlipidemia serum. RESULTS: Hyperlipidemia serum increased ICAM-1 expression on the surface of endothelial cells, and decreased NO₂^- release significantly (P＜0.01). ICAM-1 expression could be reduced and NO₂^- release could be enhanced markedly by multi-enzyme Ⅱ (P＜0.01). CONCLUSION: Multi-enzyme Ⅱ had an obvious protective effect on vascular endothelial cells which was injuried by hyperlipidemia seurm. Multi-enzyme Ⅱ could clean out oxide free radicals effectively because it had the acitive structure of both SOD and CAT.     

Effect of lncRNA FEZF1-AS1 on viability and apoptosis of LPS-induced vascular endothelial cells by regulating miR-363-3p expression

AIM To investigate the mechanism of long noncoding RNA （lncRNA） FEZF1-AS1 regulating microRNA-363-3p （miR-363-3p） on the viability and apoptosis of lipopolysaocharide （LPS）-induced vascular endothelial cells. METHODS Human umbilical vein endothelial cells （HUVECs） were cultured in vitro. pcDNA-NC, pcDNA-FEZF1-AS1, anti-miR-NC, anti-miR-363-3p, miR-NC and miR-363-3p mimics were transfected into the HUVECs and LPS stimulation was applied for 24 h. RT-qPCR was used to detect the expression of FEZF1-AS1 and miR-363-3p. The cell viability was measured by MTT assay. The apoptotic rate was analyzed by flow cytometry. The dual-luciferase reporter experiment was used to verify the targeted regulation of FEZF1-AS1 and miR-363-3p. Western blot was used to determined the expression of cyclin D1, Ki67 and cleaved caspase-3. RESULTS Compared with control group, the expression level of FEZF1-AS1 in LPS group was significantly reduced （P<0.05）, and the expression level of miR-363-3p was significantly increased （P<0.05）. Compared with pcDNA-NC+LPS group, the cell viability in pcDNA-FEZF1-AS1+LPS group was significantly increased （P<0.05）, the apoptotic rate was significantly reduced （P<0.05）, the protein levels of cyclin D1 and Ki67 were significantly increased （P<0.05）, and the protein level of cleaved caspase-3 was significantly reduced （P<0.05）. Compared with anti-miR-NC+LPS group, the cell viability in anti-miR-363-3p+LPS group was significantly increased （P<0.05）, the apoptotic rate was significantly reduced （P<0.05）, the protein levels of cyclin D1 and Ki67 were significantly increased （P<0.05）, and the protein level of cleaved caspase-3 was significantly reduced （P<0.05）. Dual-luciferase reporter experiment confirmed that FEZF1-AS1 targeted miR-363-3p. Compared with miR-NC+pcDNA-FEZF1-AS1+LPS group, the cell viability in miR-363-3p+pcDNA-FEZF1-AS1+LPS group was significantly reduced （P<0.05）, the apoptotic rate was significantly increased （P<0.05）, the protein levels of cyclin D1 and Ki67 were significantly reduced （P<0.05）, and the protein level of cleaved caspase-3 was significantly increased （P<0.05）. CONCLUSION Over-expression of FEZF1-AS1 promotes the viability and inhibits apoptosis of LPS induced vascular endothelial cells by inhibiting the expression of miR-363-3p.     

中美德系玉米品种的耐密性对深松耕作措施的响应分析

采取耕作方式×种植密度×品种三因素裂区试验,深松40 cm和旋耕15 cm耕作条件,在9.0万株/hm~2和10.5万株/hm~2种植密度下,对中系郑单958和登海618、美系先玉335和华美1号、德系KX3564和KWS2564不同血缘玉米品种的地上部形态、生理及产量构成指标进行对比分析。结果表明,深松可降低增密后玉米净光合速率、LAI、SPAD值和单株生产能力的下降幅度,缓解株型的变化,提高玉米的耐密性。我国玉米品种的耐密性对深松耕作响应与美系和德系玉米品种存在差异,深松耕作与旋耕相比,华美1号、KX3564、KWS2564、先玉335增加种植密度后,其穗位叶叶倾角、净光合速率、LAI、SPAD值下降缓慢,产量、耐密系数显著提高,其耐密适应性对深松耕作的响应度高于郑单958、登海618。