沼液兼养培养微藻潜力及不同有机碳源影响

利用沼液培养微藻可在收获藻生物质的同时回收碳、氮、磷养分,是沼液资源化利用极具潜力的途径。与光合自养相比,兼养培养可实现藻生物量快速积累,且对光、碳利用灵活,与透光性不佳的沼液相性较好,但目前缺乏相关研究论证其可行性。本文首先选取了小球藻 Chlorella sp.、蛋白核小球藻 Chlorella pyrenoidosa、栅藻 Scenedesmus sp.,以葡萄糖为碳源利用猪粪沼液对 3株微藻进行了兼养培养。结果显示,兼养策略可在大幅强化藻生物量积累的同时协同提升沼液污染物去除。其中,Chlorella pyrenoidosa展现出最佳的生物量及养分去除优势,培养7 d生物量可达1.51 g·L^-1,为光合自养的6.12倍,沼液COD、氨氮、总氮、总磷去除率较自养分别提高了20、36、41个和32个百分点。本研究进一步考察了具备两种典型碳代谢路径的有机碳源（葡萄糖-三羧酸循环,乙酸钠-乙醛酸循环）对Chlorella pyrenoidosa沼液兼养培养的影响,发现葡萄糖相较于乙酸钠更适宜作为沼液兼养培养的有机碳源,且葡萄糖浓度与利用效率呈负相关,1 g·L^-1葡萄糖浓度条件下Chlorella pyrenoidosa具有最高的单位有机碳生物量产率。此外,兼养微藻通过代谢葡萄糖可协同提升光合性能,使PSⅡ最大量子产量、实际量子产量、调节性能量耗散量子产量等维持较高水平,既弥补了沼液弱透光下光能不足,也强化了持续光照后的光系统损伤恢复机制。因此,本研究认为以添加1 g·L^-1葡萄糖的沼液兼养培养Chlorella pyrenoidosa是克服沼液养藻光衰减等不利因素,强化微藻生物量产量及养分回收效率的有效方式,在畜禽养殖场沼液生物消纳与资源化利用方面有较好的应用前景。     

28%多·井悬浮剂防治水稻纹枯病田间药效评价

为明确28%多.井悬浮剂对水稻纹枯病的防治效果,进行田间药效试验。结果表明：28%多.井悬浮剂对水稻纹枯病有显著的防治效果,按500g/hm^2用量,第三次药后14d对纹枯病的防效为86.13%,与常用药剂5%井冈霉素水剂3.75L/hm^2的防效相当,而且对水稻安全,值得推广应用。     

β-甘露聚糖酶基因重组整合组成型表达载体的构建

应用PCR方法从P.pastorisGS115染色体中扩增了GAP启动子(PGAP),大小为500bp左右,以其取代诱导型表达载体pPIC9K上的AOX1启动子(PAOX1),构建了组成型表达载体pGAP;再从野生型酵母菌JSY4染色体中扩增出25S rDNA保守序列,大小为1 700bp左右,以其取代组成型表达pGAP上的组氨酸脱氢酶基因(H IS4)片断,构建了整合组成型表达载体pGAP-rDNA。再双酶切重组质粒pT002M anⅠ得编码β-甘露聚糖酶的ManⅠ基因片断插入pGAP-rDNA的多克隆位点(MCS),获得含有目的基因ManⅠ的重组整合组成型表达载体pGAP-rDNA-ManⅠ。CaC l2法转化感受态大肠杆菌DH5α,对阳性克隆进行质粒PCR鉴定和单、双酶切鉴定。结果表明:成功构建了重组组成型表达载体pGAP-rDNA-ManⅠ,为下一步野生型酵母菌JSY4中β-甘露聚糖酶的组成型表达打下基础。     

Feeding Solanum glaucophyllum to preparturient multiparous cows prevents postparturient hypocalcemia

Solanum glaucophyllum (SG) contains 1,25‐dihydroxyvitamin D₃ (1,25‐(OH)₂D₃) glycosides. We investigated the effect of SG on hypocalcemia in cows. Serum levels of 1,25‐(OH)₂D₃, total calcium and phosphorus dose‐relatedly increased after feeding with SG, while serum magnesium and chloride levels fell (P < 0.05). We also performed an ethylenediaminetetraacetic acid (EDTA) infusion to induce artificial hypocalcemia. Cows that had been fed 4.0 mg/kg body weight of SG daily for 2 weeks had a higher serum concentration of total calcium at the end of EDTA infusion than those not fed SG (P < 0.05). In a field trial, multiparous cows were assigned to one of four groups: (1) no SG, (2) 1.3 g or (3) 2.6 g of SG daily from 14 days before the estimated calving day until 3 days after calving, or (4) a single feed of 35.75 g SG at 3 days before the estimated calving day. The concentrations of serum total calcium after the calving in each treatment group were (1) 7.4, (2) 7.9, (3) 8.0 and (4) 8.9 mg/dL and higher for (4) than for (1) (P < 0.05). The data suggests that feeding a high dose of SG before the calving may maintain higher concentrations of serum calcium after the calving.     

意蜂采用2,3日龄工蜂幼虫产浆的研究

对意蜂采用２和３日龄工蜂幼虫产浆的王台接受率和不同时间取浆浆量进行了研究。研究结果显示：①２日龄工蜂幼虫的王台接受率（８２．４２％）与采用３日龄幼虫的（８１．２１％）无显著差异;②２和３日龄幼虫产浆的台平均产浆量最高峰分别在各自移虫后第６０小时和第４８小时,浆量较高时段分别在移虫后上时和第４２－５４小时;③２日龄幼虫产浆最高时段台平产浆量（０．３７５４ｇ）极显著高于３日龄的（０．３１５７ｇ）但采用     

鸡溶菌酶基因3＇端MAR在同源细胞系对基因表达调控的研究

用带有鸡溶菌酶基因增强子（Ｅ）和启动子（Ｐ）的编码细菌氯霉素乙酰基转移酶（ＣＡＴ）的融合基因（ＥＰＣ），在其上游区、下游区或在上游和下游区同时插入鸡溶菌酶基因３＇端核基质附着区（ＭＡＲ）的不同表达载体ＭＥＰＣ、ＥＰＣＭ和ＭＥＰＣＭ，稳定转染鸡ＨＤ１１Ｐｒｏｍａｃｒｏｐｈａｇｅ同源细胞系，筛选不同表达载体稳定整合后的细胞株，检测ＣＡＴ表达水平，确定其表达基因拷贝数，从而分析鸡溶菌酶基因３＇端ＭＡＲ对基因表达的影响。稳定整合表达和瞬时表达实验结果表明，鸡溶菌酶基因３＇端ＭＡＲ在同源细胞系对基因表达没有激活作用，与该基因５＇端ＭＡＲ在同源或异源细胞系中能激活基因表达形成鲜明对照，说明５＇瑞ＭＡＲ和３＇端ＭＡＲ在调节鸡溶菌酶基因表达上存在一种协调关系。     

3％高渗苯氧威防治春尺蠖试验

利用2000倍液、3000倍液、4000倍液3个不同体积分数的3％高渗苯氧威进行了室内、室外防治春尺蠖幼虫试验,结果表明：施药72h后,室内试验的3个体积分数平均死亡率均达到100．0％;室外试验以2000倍液和3000倍液死亡率为最高,达到98．5％,防治效果显著。3％高渗苯氧威是理想的防治春尺蠖的仿生物杀虫剂。     

Effect of tetrandrine on radiosensitivity of nasopharyngeal carcinoma cells

AIM: To investigate the mechanism of the radiosensitizing effect of maximum non-cytotoxic doses of tetrandrine (Tet) on nasopharyngeal carcinoma cell lines CNE1 and CNE2.METHODS: The cells were treated with ma-ximum non-cytotoxic doses of Tet (for CNE1 cells at 1.5 μmol/L and for CNE2 cells at 1.8 μmol/L), irradiation at 4 Gy, or combination of irradiation and maximum non-cytotoxic doses of Tet. The cell cycle distribution was analyzed by flow cytometry. The protein levels of γ-H2AX, cleaved caspase-3, p-CDC25C, CDK1, p-CDK1, cyclin B1, ERK and p-ERK were determined by Western blot.RESULTS: The expression of γ-H2AX was increased in CNE1 cells and CNE2 cells after combined treatment with irradiation and maximum non-cytotoxic doses of Tet. The percentages of CNE1 cells and CNE2 cells at G₂/M phase in irradiation group were (18.09±0.42)% and (18.48±1.32)%, respectively, which were decreased to (15.88±1.04)% and (13.80±0.82)% in combined treatment group, respectively (P<0.05). Combined treatment enhanced the increase in the protein level of cleaved caspase-3 caused by irradiation. The protein levels of p-CDC25C and p-CDK1 were increased in a dose-dependent manner by Tet treatment (P<0.05), while the expression of CDK1 showed no difference among different doses of Tet treatments. The protein levels of p-CDC25C, p-CDK1 and CDK1 showed no difference after the treatment with maximum non-cytotoxic doses of Tet. The combined treatment with irradiation and the maximum non-cytotoxic doses of Tet decreased the protein levels of p-CDC25C and p-CDK1 (P<0.05), increased the expression of cyclin B1, and had no influence on the expression of CDK1 (P<0.05). The combined treatment resulted in an increase in the protein level of p-ERK1 (P<0.05).CONCLUSION: The maximum non-cytotoxic doses of Tet enhance the DNA damage and apoptosis in CNE1 cells and CNE2 cells caused by irradiation, and the mechanism might be associated with ending of G₂/M arrest via activation of ERK/CDC25C/CDK1/cyclin B1 pathways.     

Intestinal absorption of forsythoside A in different compositions of Shuang-Huang-Lian

Shuang-Huang-Lian (SHL), a traditional Chinese formula containing Lonicerae japonicae flos (LJF), Scutellariae radix (SR) and Forsythiae fructus (FF), is commonly used to treat acute upper respiratory tract infection, acute bronchitis and light pneumonia. Forsythoside A is one of the main active ingredients in Forsythiae fructus, a key herb in SHL. In the present study, effects of different compositions in SHL on the intestinal absorption of forsythoside A were investigated. The observations from in situ intestinal circulation model showed that A/%(h^− 1) of forsythoside A in FF + LSF, FF + SR and SHL were all reduced greatly compared with that in FF. However, in pharmacokinetics study, C_max and AUC_0 → 1440 of forsythoside A all increased and T_1/2 prolonged in SHL, FF + LJF and FF + SR compared with FF. The results indicated that the different compositions of SHL decreased absorption but increased bioavailability of forsythoside A, which may be related to its metabolism inhibited in intestine or liver.