杨桃果实生长发育过程中营养品质的变化

杨桃（Averrhoa arambola L．）为华南地区重要的热带水果。本试材为华南农业大学园艺分场种植的3年生盆栽马来西亚甜杨桃，砧木为酸杨桃。在杨桃的开花期，选择生长势、开花数量和时间较一致45株为试材，再选择受精时间一致的果实做标记。采样时问从开花后（2003年7月15日）至杨桃充分成熟（2003年10月25）。测定杨桃果实中的糖（蒽酮比色法）、有机酸（HPLC法）、维生素C（2，6-二氯靛酚钠滴定法）和单宁（高锰酸钾滴定法）的含量。     

黑穗醋栗新品种‘甜蜜’

 ‘甜蜜’是从波兰引进的黑穗醋栗试材中筛选出来的晚熟品种, 生长势强, 果穗长, 单果质量1.47 g, 可溶性固形物14% , 维生素C 1.6 g/kg FM。果实出汁率70%。风味酸甜, 鲜食口味佳。丰产性好。在长春地区7月中下旬成熟。     

嫁接西瓜肥料试验初报

试验结果表明,在土壤有机质含量高达4.07%的单栋钢管大棚中,进行嫁接西瓜栽培时,与常规施肥量相比,在4个减肥处理中,以减量20%的处理增产优质效果最佳。     

彩色甜椒花药培养若干影响因子的研究

利用硝酸银、ATP钠盐、NAA、KT进行了四因素三水平正交试验,材料为彩色甜椒品种7160的花药。结果表明,硝酸银是影响彩色甜椒花药培养胚状体诱导率的最主要因素,在其浓度为1.0mg/L时胚状体诱导率最高;ATP钠盐为次主要因素,在其浓度为100.0mg/L时效果最好。KT比NAA对胚状体诱导率的影响大;KT浓度1.0或1.5mg/L时较好。     

人为影响下古尔班通古特沙漠小尺度生态环境变化

随着沙漠中油气资源勘探开发、公路建设和重大工程相继实施 ,对生态环境的人为影响日益加深。本文以重大工程实验点为例 ,通过研究对比工程影响区内人工沙垄和自然沙垄的砂质新成土理化性状和植被群落特征 ,指出了沙漠生态环境在人为干扰下发生的一系列变化 ,以及受损生态环境在人们采取积极补救措施的情况下所具有的自然修复能力     

Insulin induced LPL mRNA expression in THP-1 macrophage and acceleration of transferring the macrophage to foam cell

AIM:To investigate the effect of insulin on ox-LDL transferring the THP-1 cells to foam cells and influencing the LPL mRNA expression in THP-1 cells.METHODS:THP-1 cells were incubated with 50 mg/Lox-LDL and insulin at concentrations of 10 mU/L, 100 mU/L, 1 000 mU/L and 10 000 mU/L, respectively. The expression of LPL mRNA in cells was detected by RT-PCR. Lipoprotein lipase of THP-1 cells was presented by no-specific lipase staining. THP-1 cells were stained with oil red O. Accumulation of total cholesterol (TC) in THP-1 cells was determined with oxidase assay.RESULTS:In 100 mU/L、1 000 mU/L、10 000 mU/L insulin groups, LPL mRNA expression increased 2 times, the average cell perilength was longer, the percentage of positive oil red O staining cells was significant higher, the content of cholesterol in THP-1 cells was higher than in ox-LDL control (P＜0.05).CONCLUSION:Insulin accelerates transferring of THP-1 cells to foam cell with exposed to ox-LDL because LPL mRNA expression increased in the cells.     

Bcl-2 antisense oligodeoxynucleotide increases the sensitivity of HL60 and K562 cells to daunorubicin

AIM:To investigate whether the bcl-2 antisense oligonucleotide increases the sensitivity of HL60 and K562 cell lines to daunorubicin.METHODS:IC50 for HL60 and K562 was determined with MTT method, the expression levels of Bcl-2 protein were assayed by immunofluorescence using fluoresce isothiocyanate labeling. In addition, apoptosis was detected by morphological observation and flow cytometric analysis of DNA fragmentation.RESULTS:It was found that the two oligonucleotides directed against the coding region and the translation initiation of bcl-2 mRNA, combined respectively with daunorubicin, inhibited expression of bcl-2 protein, increased apoptosis in HL60 and K562 cells, and decreased IC50 of daunorubicin significantly (P＜0.05). Compared to the antisense oligonucleotide directed against the translation initiation of bcl-2 mRNA, the antisense oligonucleotide directed against the coding region showed stronger effects in the aspects of increasing the sensitivity of HL60 cells to daunorubicin (P＜0.05).CONCLUSIONS:These two antisense sequences in the translation initiation and the coding region of bcl-2 mRNA increased the sensitivity of HL60 and K562 cell lines to daunorubicin in a sequence-specific manner.     

Biological characteristics of long passaging rat mesenchymal stem cells

AIM:To investigate multi-potential of rat bone marrow mesenchymal stem cells (rBMMSC) and mutation inclination, the rBMMSC were long passaged in vitro. METHODS:Cellular cycles of different passages were assayed by FACSan flow cytometry and karyotypes of passage 6, passage 25 and passage 45 were compared by G-binding analysis. RESULTS:The early passages and long-term passages all showed strong proliferation; passage 6, passage 25 and passage 45 all showed normal karyotype. CONCLUSION:Long-term culture and passage of rBMMSC still remains strong proliferation. With this capability, the mutation inclination is not enhanced.     

Effect of tea-polyphenols on the activation of NF-κB and the expression of TGF-β1 mRNA in THP-1 cells incubated with VLDL,LDL or ox-LDL

AIM:To investigate the effect of tea-polyphenols (TP) on the activation of NF-κB and the expression of TGF-β₁ mRNA in THP-1 cells (a human acute monocytic leukemia cell line). METHODS:THP-1 cells were incubated with the different concentrations of TP, VLDL, LDL or ox-LDL. In the THP-1 cellls, the nuclear malposition rate of NF-κB was detected with immunohistochemistry technique, the positive index of the TGF-β₁ mRNA expression was detected by hybridization in situ, and accumulation of total cholesterol (TC) in cells incubated with 0.4-40 μg/L TP was determined with oxidase assay. RESULTS:The nuclear malposition rate of NF-κB, the positive index of the TGF-β₁ mRNA expression and TC in THP-1 cells incubated with 0.4-40 μg/L of TP were lower than those with 0 μg/L of TP in TP-V group, TP-L group and TP-O (P＜0.05). The differences of these markers in THP-1 cells incubated with more than 40 μg/L TP in TP-V group, TP-L group and TP-O were not statistically significant, compared with TP-C group (P＞0.05). CONCLUSION:TP inhibited the activation of NF-κB, the expression of TGF-β₁ mRNA and the foam cell formation in the mono-macrophage.     

镧素对镰刀菌Fusarium solani及其致病酶的影响

采用琼脂平板生长速率法及液体培养基培养测定了La对镰刀菌Fusarium solani的抑制作用和毒力,并测定了其对病菌胞外的果胶酶、蛋白酶和纤维素酶等几种致病酶活性的影响。结果表明,随着La2O3浓度升高,对病菌菌丝生长的抑制作用增强,对病菌的EC50和EC95分别为278.2和552.0 mg/L;在一定浓度范围内,La提高了单位量菌丝所产生3种致病酶的活性,但由于菌丝生长受到抑制,除蛋白酶外,病菌胞外致病酶果胶酶和纤维素酶的总量或总活性受到了抑制,降低了病菌的致病力。