鱼类肝脏酯酶的同工酶构成及其对磷酸三苯酯和马拉氧磷的敏感性

用聚丙烯酰胺凝胶电泳法分离了麦穗鱼 (Pseudorasbora p arva)、金鱼 (Carassius auratus)、尼罗罗非鱼 (Tilapja nilotica)、食蚊鱼 (Gambusia affinis)、虹鳟 (Salmo gairdneri)等五种鱼的肝脏酯酶的同工酶 ,以乙酸α-萘酯为底物测定了它们的活性。在麦穗鱼、金鱼、尼罗罗非鱼体内发现两条酶带 ,在食蚊鱼和虹鳟体内发现一条酶带。离体抑制率实验表明 ,五种鱼肝脏内均含有对磷酸三苯酶敏感的酶带 ,而对马拉氧磷敏感的酶带只存在于麦穗鱼、金鱼、尼罗罗非鱼体内。酯酶同工酶分布型的意义及与马拉硫磷选择毒性的关系在本文中进行了讨论。     

植物生长调节剂DTA-6对花生产量、品质及其根系生理调控研究

在大田栽培条件下,经过3年试验,研究了在花针期叶面喷施植物生长调节剂DTA-6对花生产量、品质及器官生理功能的影响。结果表明:与清水对照比较,DTA-6可显著增加荚果和籽仁产量,表现在单株干物质增加,饱荚数、饱荚重和籽仁重显著提高,秕荚数显著减少;DTA-6对籽仁中含油量具有促进作用,而对游离氨基酸、蛋白质含量有降低的趋势;同时DTA-6提高了花生的根系活力和根系伤流量以及根系的吸收和合成能力,提高了花生的结瘤性和固氮能力。     

Repression of deoxynivalenol accumulation and expression of Tri genes in Fusarium culmorum by fungicides in vitro

A defined medium was developed in which to monitor deoxynivalenol (DON) accumulation, fungal growth and expression of genes involved in trichothecene biosynthesis (designated Tri genes). In liquid culture, DON accumulated shortly after maximum expression of Tri6 and coincident with expression of Tri5. This was generally 96 h after inoculation. The effects of sublethal concentrations of the fungicides azoxystrobin, trifloxystrobin, kresoxim-methyl and tebuconazole on biosynthesis of the trichothecene DON by Fusarium culmorum were studied using this medium. The strobilurin fungicides trifloxystrobin and azoxystrobin significantly reduced the accumulation of DON in culture medium at a range of concentrations. Kresoxim-methyl, also a strobilurin, and tebuconazole, a triazole, did not significantly reduce the accumulation of DON, although levels were lower than those in nonamended cultures. Trifloxystrobin significantly reduced the accumulation of DON when added to cultures before initiation of trichothecene biosynthesis. RT-PCR assays of the expression of Tri6 and Tri5 genes indicated that trifloxystrobin acted by inhibiting the initiation of trichothecene biosynthesis.     

草炭对土壤中尿素中氮的动态影响

采用室内培养,研究了两种草炭对尿素在土壤中转化后的铵态氮和碱解动态变化的影响以及其原因。表明,不论是石河子草炭或是加拿大草炭,在抑制尿素硝化产生硝态氮的同时对氨的挥发有一定的抑制作用,土壤在较长的内（２周内）保持较高的铵态氮含量,草炭的加入活跃了土壤中微生物,减少了肥料氮素的损失。     

洱源丛枝瑚杀虫活性成分研究

洱源丛枝瑚(Ramaria eryuanensis)石油醚萃取物经过柱层析得到单体化合物B8,该化合物对小菜蛾3龄幼虫72 h的LC50为3.375 7 mg/mL。经FAB-MS、1HNMR、13CNMR及DEPT等波谱鉴定,并与文献值对照,确定其为麦角甾-7,22-二烯-3β,5α,6β-三醇。     

苜蓿盲蝽属三种害虫对环氧虫啶的敏感性

环氧虫啶是我国自主研发的一种新型的新烟碱杀虫剂,主要用于防治刺吸式口器害虫。本文采用点滴法测定了环氧虫啶对中黑盲蝽、苜蓿盲蝽、三点盲蝽的毒力,结果表明,三种盲蝽对环氧虫啶均具有较高的敏感性,其中中黑盲蝽的敏感性最高,LD_(50)值为2.03ng/头,其次为苜蓿盲蝽和三点盲蝽,LD_(50)分别为3.12和3.34ng/头。多功能氧化酶抑制剂PBO能明显增加环氧虫啶对三种盲蝽的毒力,谷胱甘肽S-转移酶抑制剂DEM只在中黑盲蝽上对环氧虫啶表现出增效作用,而羧酸酯酶抑制剂TPP未显示增效作用。这说明,环氧虫啶具有防治苜蓿盲蝽属三种害虫的应用潜力,细胞色素P450-单加氧酶可能在环氧虫啶代谢中起重要作用。     

抗青枯病番茄砧木品种宝砧6号的选育

宝砧6号是以自交系Y0609-4-6为母本,自交系T0802-7-4为父本配置而成的番茄砧木一代杂交种。该品种为无限生长型,生长旺盛,茎秆粗壮,株型紧凑,高抗青枯病;与生产上主栽品种嫁接亲和性好,对果实品质、商品性无不良影响,作砧木嫁接栽培抗青枯病和抗早衰能力效果明显,嫁接种植田后期可延长采收15~20 d,增产幅度超过15%。目前该品种已成为资源车田、永福三皇等番茄产业基地嫁接砧木的主要应用品种,推广应用面积达400 hm~2。     

苹果6–磷酸葡萄糖酸脱氢酶基因Md6PGDH1的克隆和功能分析

以‘嘎拉’苹果为材料,克隆了6–磷酸葡萄糖酸脱氢酶基因Md6PGDH1(序列号:MDP0000279299)全长。序列分析显示,该基因包含一个长为1 047 bp完整的开放阅读框,编码347个氨基酸,分子量为36.430 k D,预测等电点为9.24。同源性分析表明Md6PGDH1还有另外3个同源基因;功能域分析表明Md6PGDH蛋白含有两个保守的绑定域;亚细胞预测表明Md6PGDH定位存在差异。分析Md6PGDH1启动子发现存在多个响应非生物胁迫的顺式作用元件。定量分析显示,Md6PGDH1在苹果的不同组织中都有表达,且受非生物胁迫诱导。原核诱导Md6PGDH1蛋白并进行蛋白酶活的测定,为后续蛋白功能鉴定奠定了基础。Md6PGDH1在苹果愈伤组织中过量表达,提高其抗盐胁迫的能力。     

Suberoylanilide hydroxamic acid induces apoptosis of HepG2 cells by endoplasmic reticulum stress apoptotic pathway

AIM: To investigate the effect of suberoylanilide hydroxamic acid (SAHA) on the proliferation and apoptosis of human hepatocellular carcinoma HepG2 cells and to explore its possible mechanism. METHODS: HepG2 cells were treated with SAHA at different concentrations for 48 h. The proliferation of HepG2 cells was detected by real-time cellular analysis. The protein levels of acetylated histones H3K9 and H3K27, glucose-regulated protein 78 (GRP78), protein kinase R-like endoplasmic reticulum kinase (PERK) and p-PERK were determined by Western blot. The cell apoptosis was analyzed by flow cytometry. RESULTS: Compared with control group, treatment with SAHA at 0.1 μmol/L and 1 μmol/L for 48 h showed no significant inhibitory effect on the proliferation of HepG2 cells, while SAHA at 6 μmol/L and 12 μmol/L significantly inhibited the proliferation of HepG2 cells (P<0.05). The results of Western blot showed that the protein levels of acH3K9, acH3K27, GRP78 and p-PERK increased significantly after treated with SAHA at diffe-rent concentrations for 48 h, while the protein level of PERK was decreased significantly (P<0.05). The results of flow cytometry analysis showed that the apoptotic rates of the HepG2 cells increased with the increase in SAHA concentration. CONCLUSION: SAHA up-regulates the acetylation of H3K9 and H3K27 in the HepG2 cells and induces apoptosis of HepG2 cells by activating the endoplasmic reticulum stress-related apoptosis pathway.