不同春玉米品种茎秆显微结构对抗折强度的响应

以冀西北寒旱区9个春玉米品种为研究对象,通过测定玉米基部第3节抗折强度,利用光学显微镜观察其茎节显微结构,对维管束各项显微指标与节折强度进行相关分析,研究春玉米节折强度与茎秆显微结构之间的关系。结果表明,不同春玉米品种间节折强度达显著水平。对各品种维管束显微指标进行统计分析表明,维管束鞘厚度和表皮细胞厚度变异系数最大,分别达到34.8%和23.2%;茎节维管束数目增多不利于节折强度的提高(r=-0.945**,r=-0.927**),维管束平均面积、韧皮部面积增大有利于节折强度的增加(r=0.831*,r=0.799*;r=0.733*,r=0.786*)。通径分析表明,维管束数目对节折强度的直接效应最大,表皮细胞厚度次之,维管束最大面积、维管束鞘厚度、韧皮部面积等指标也通过维管束数目对茎折强度起间接作用。参试品种中,京农科728、纪元108维管束数目较少,维管束平均面积、韧皮部面积较大,茎折强度较高,抗倒伏性优于其他品种。     

Roles of protein phosphatase 4 in down-regulation of eNOS Ser633 phosphorylation induced by palmitic acid in human umbilical vein endotheli?al cells

AIMTo investigate the roles of protein phosphatase 4 (PP4) in down-regulation of endothelial nitric oxide synthase (eNOS) Ser633 phosphorylation induced by palmitic acid (PA). METHODSHuman umbilical vein endothelial cells (HUVECs) were treated with PA at 25 μmol/L, 50 μmol/L, 100 μmol/L and 200μmol/L for 36 h, or treated with PA at 100 μmol/L for 12 h, 24 h, 36 h and 48 h. Protein phosphatase 2A (PP2A) family inhibitor fostriecin (FST, 20 nmol/L) or okadaic acid (OA, 5 nmol/L) was selected to pretreat the HUVECs for 30 min. Protein phosphatase 4 catalytic subunit (PP4c) siRNA or protein phosphatase 2A catalytic subunit (PP2Ac) siRNA was transfected into the HUVECs. The protein expression levels of of eNOS, PP4c and PP2Ac, as well as the level of eNOS Ser633 phosphorylation, were detected by Western blot. The intracellular nitric oxide (NO) content was measured by DAF-FM DA. RESULTS(1) Compared with control group, the levels of eNOS Ser633 phosphorylation were decreased in PA groups in which the HUVECs were treated with 25 μmol/L, 50 μmol/L, 100 μmol/L and 200 μmol/L PA for 36 h (P<0.05) and 100 μmol/L PA for 24 h, 36 h and 48 h (P<0.05). No significant difference in the level of total eNOS protein expression among all the groups was observed. (2) Compared with control group, both FST and OA pretreatment reversed the reduction of eNOS Ser633 phosphorylation (P<0.05) and the decrease in intracellular NO content (P<0.05) induced by PA. No significant difference in the level of total eNOS protein expression among all the groups was observed. (3) Compared with si-Control group, the PP4c protein expression was significantly reduced (P<0.05), while the level of eNOS Ser633 phosphorylation was significantly increased in si-PP4c group (P<0.05). Although the levels of PP2Ac protein expression declined significantly (P<0.05), the level of eNOS Ser633 phosphorylation remained unchanged in si-PP2Ac group. No significant differencein the level of total eNOS protein expression among all the groups was found. CONCLUSION PA significantly reduces the level of eNOS Ser633 phosphorylation and the content of NO in the HUVECs, which may be due to PA inducing the activation of the PP2A family member PP4 rather than PP2A.     

Down-regulation of miR-153-3p attenuates H2O2-induced H9C2 cell injury by promoting Nrf2 expression

AIM To study the effect of microRNA-153-3p (miR-153-3p) knock-down on oxidative injury of H9C2 cells induced by H₂O₂ and its specific mechanism. METHODS The oxidative stress injury of H9C2 cell model was induced by H₂O₂, and then the cell viability and the expression of miR-153-3p were detected by MTT assay and RT-qPCR, respectively. The effects of miR-153-3p knock-down on the H9C2 cell injury under oxidative stress were studied by RNA interference technology. The targets of miR-153-3p were identified by Western blot and dual-luciferase reporter assay. RESULTS MTT assay showed that the viability of H9C2 cells was decreased with the increase in H₂O₂ concentration (P<0.05). The results of RT-qPCR showed that the expression of miR-153-3p was increased with the increase in H₂O₂ concentration (P<0.05). Knock-down of miR-153-3p increased the viability of H9C2 cells under oxidative stress, decreased the cell apoptosis and the content of malondialdehyde (MDA), and increased the activity of superoxide dismutase (SOD). The expression of nuclear factor E2-related factor 2（Nrf2） and antioxidant response element（ARE） activity were increased with the increase in H₂O₂ concentration (P<0.01). TargetScan analysis and dual-luciferase reporter assay showed that Nrf2 was one of the potential target genes of miR-153-3p. The results of Western blot further showed that over-expression of miR-153-3p inhibited the expression of Nrf2 (P<0.01), while down-regulation of miR-153-3p increased the expression of Nrf2 (P<0.01). Dual interference with Nrf2 and miR-153-3p significantly reduced H9C2 cell viability, promoted the apoptosis, increased MDA content, and decreased SOD activity in the presence of H₂O₂ (P<0.01). CONCLUSION Inhibition of miR-153-3p expression attenuates the injury of H9C2 cells induced by H₂O₂ through up-regulating Nrf2/ARE signaling pathway.     

蜡梅花离体摊放过程中香气感官评价和挥发性物质分析

蜡梅花是重要的天然花香原料。采用顶空—固相微萃取和气相色谱—质谱联用技术（HS–SPME–GC–MS）结合感官审评,分析了采摘后蜡梅花摊放过程中挥发性物质的变化规律。结果表明,离体蜡梅花在摊放过程中开放状态变化不明显,花枝经清水培养,花苞到全开状态历经32 h左右。全开状态蜡梅花的挥发性物质种类随摊放时间的延长呈先增加后降低的趋势,摊放12 h最多,此时出现了酮类、醛类和酚类;大部分挥发性物质相对含量在摊放20 h后降低。主要挥发性物质乙酸苄酯在摊放12 h达峰值,较0 h增加35.04%;4–乙基苄醇和α–罗勒烯呈现先增加后降低的趋势;α–罗勒烯在摊放4 h后急剧增加,20 h达最大值;芳樟醇、别罗勒烯和2,6–二甲基–2,4,6–辛三烯在摊放24 h内呈降低趋势,分别较0 h下降了18.32%、78.92%和41.19%。结合感官审评与GC–MS分析结果可知,全开状态的蜡梅花采摘后离体摊放20 h内能较好地保持花香的鲜灵度和浓郁度,且在12 ~ 20 h之间挥发性物质种类丰富,具花果香的挥发性物质相对含量较高。研究结果可为蜡梅花作为天然花香原料的更有效利用提供理论参考。     

梁山慈竹新品种‘西科1号’

‘西科1号’是由梁山慈竹（Dendrocalamus farinosus）通过甲基磺酸乙酯诱变,再进一步筛选出的新品种。一年生竹秆厚被少量白粉,多年生的主枝不明显,纤维素含量高（55.28%）,木质素含量低（20.02%）,良浆得率高（39.29%）,硫酸盐浆的撕裂指数大（16.96 mN · m² · g^-1）,耐折度强（2.1）,竹材性能好,笋营养丰富,且具有一定观赏性,是优质的工业用、笋用和观赏用竹种。     

酿酒山葡萄新品种‘紫晶甘露’

‘紫晶甘露’是以优质酿酒山葡萄酒品种‘左山二’为母本,‘哈桑’为父本杂交选育而成的能够单品种酿造干红酒的山葡萄新品种。果穗圆锥形,有岐肩或副穗。果实圆球形,果皮黑色,果肉绿色,无肉囊,种子2 ~ 4粒。生长势强,抗寒、抗病性极强,4年丰产,4 ~ 6年平均产量1 876 kg • km-2。果实可溶性固形物含量达到21.0%,总酸11.6 g • L-1,出汁率65.5%。     

利用酵母双杂交膜系统筛选与小麦蓝矮植原体免疫膜蛋白互作的异沙叶蝉蛋白

正小麦蓝矮病(Wheat blue dwarf,WBD)是我国西北麦区一种重要植原体病害,在我国西部地区危害严重。该病害由异沙叶蝉(Psammotettix alienus L.)专化性传播,介体传毒成为病害流行的重要中心环节[1]。本实验室前期通过免疫荧光标记研究发现WBD植原体免疫膜蛋白(immunodominant membrane protein, IMP)与介体异沙叶蝉肌动蛋白互作,说明IMP在植原体传播和致病过程中起关键作用。     

4种不同性诱剂对玉米草地贪夜蛾诱集作用

为准确掌握草地贪夜蛾成虫发生动态,筛选对当地种群专一性强、灵敏度高的性诱剂,对深圳百乐宝生物农业科技有限公司(BLB)、宁波纽康生物技术有限公司(NK)、江苏宁录科技股份有限公司(NL)、南京新安中绿生物科技有限公司(XAZL)4个厂家生产的草地贪夜蛾性诱剂在江苏盐城市大丰区进行田间诱捕效果试验,探讨草地贪夜蛾性诱剂的使用技术。结果表明:4种不同性诱剂诱芯对草地贪夜蛾的诱集效果存在明显差异。BLB诱芯和NL诱芯可以有效监测草地贪夜蛾成虫田间发生动态,羽化高峰期明显,且峰值日期一致,NK诱芯诱集的成虫虫峰不明显,XAZL诱芯零星诱到成虫,无明显成虫高峰;BLB诱芯监测期内日均诱蛾量、最高单次诱蛾量、总诱蛾量均显著高于其他3种诱芯,其总诱蛾量达136.75头,分别是NL诱芯、NK诱芯、XAZL诱芯的1.47倍、4.76倍、10.52倍;通过对BLB诱芯进行持续30 d和持续60 d的诱捕对比试验,发现BLB诱芯1~30 d内诱捕性能稳定,诱蛾量大,31~60 d内日均诱蛾量、最高单次诱蛾量、总诱蛾量均有所下降且达显著水平,尤其是50 d后诱捕量下降明显。结果表明:BLB诱芯的诱蛾量大,能够明显反映出草地贪夜蛾的羽化高峰期,符合测报要求,更适合本地区草地贪夜蛾的监测,使用该诱芯时建议30 d更换1次。     

东省不同地区玉米内生真菌的群落组成和多样性分析

为探究山东省玉米内生真菌的资源分布、群落组成及多样性,采用叶片组织分离法对山东省52个市县的玉米内生真菌进行分离纯化,通过内转录间隔区（internal transcribed spacer,ITS）序列分析技术进行内生真菌的种属鉴定,并分析内生真菌的群落组成和多样性。结果表明,共分离到857株内生真菌,隶属25个属,其中链格孢属Alternaria的菌株数量最多,为583株,占总菌株数的68.03%,其次为镰刀菌属Fusarium有71株,占总菌株数的8.28%;大部分地区的优势属为链格孢属,少数地区的优势属为镰刀菌属、炭疽菌属Colletotrichum和弯孢属Curvularia。不同地区的内生真菌定殖率变化很大,在12.50%~100.00%之间,平均定殖率为76.15%;陵城的多样性指数和均匀度指数最高,分别为1.74和0.97;莱芜的丰富度指数最高为2.22。山东省玉米内生真菌可以分为5个类群,其中黄河流域地区内生真菌定殖率相对较高。表明山东省玉米内生真菌种类丰富,不同地区间多样性水平存在差异。     

响应面法优化纳豆混合发酵工艺的研究

为了改善纳豆的风味和口感,提高其可食用性,通过优化纳豆芽孢杆菌与酿酒酵母混合发酵工艺,降低纳豆的氨腥味;在此基础上,利用单因素试验和响应面法对纳豆固态发酵条件进行优化。确定纳豆固态发酵的最优条件为:混合菌种比例为3∶1,大豆含水量为60%,大豆的铺层厚度为3 cm,高温蒸煮30 min,接种量6%,发酵温度35℃,发酵时间28 h,后熟1 d,此条件下,挥发性盐基氮含量降低了40.1%,纳豆激酶活力提高了39.1%,纳豆的风味和口感均得到提升,更适合我国居民食用。