拔节后补灌对不同穗型冬小麦耗水和籽粒产量的影响

为探究拔节期和开花期不同补灌方案对不同穗型冬小麦耗水特性、籽粒产量和水分利用效率的影响,于2017-2019年在山东省泰安市以大穗型品种山农23和中多穗型品种山农29为试验材料,以拔节后无灌水(T1)为对照,设置拔节期补灌目标为0~20 cm土层相对含水率达100%田间持水率(T2)、拔节期和开花期补灌目标为0~20 cm土层相对含水率达100%田间持水率(T3)和拔节期补灌目标为0~40 cm土层相对含水率达100%田间持水率(T4) 3种补灌方案。结果表明,拔节后不同补灌方案对大穗型和多穗型小麦品种影响基本一致。与T1处理相比,T4处理显著提高了0~100 cm土层土壤相对含水率,使60~100 cm土层土壤相对含水率在开花期仍保持较高水平;T3处理显著提高了拔节期0～60 cm和开花期0~40 cm土层土壤相对含水率。与T3处理相比,T4处理的拔节至开花阶段耗水量增加了28.9%,其中对上层土壤总供水的表观消耗量增加了66.4%;T4处理在开花至成熟阶段对深层土壤总供水的表观消耗量增加了68.0%,对上层土壤总供水的表观消耗量降低了37.4%。在开花至成熟期降水较多(121.2 mm)的年份,T4处理的开花至成熟阶段耗水量、开花后旗叶净光合速率和籽粒产量相对于T3处理均无显著变化,但总耗水量较高,水分利用效率显著降低;在开花至成熟期降水较少(45.2 mm)的年份,T4处理的开花至成熟期的阶段耗水量、开花后旗叶净光合速率、籽粒产量和水分利用效率较T3处理均显著降低。因此,在小麦全生育期降水量为111.6~220.2 mm、开花后降水量为45.2~121.2 mm的条件下,大穗型和中多穗型小麦品种均以在拔节期和开花期将0~20 cm土层补灌至100%田间持水率的补灌方案最优,可同时实现高产和高水分利用效率。     

云南省水稻稻瘟病菌无毒基因AVR-Pia变异及水稻抗性基因Pia的有效性

为进一步了解田间稻瘟病菌Magnaporthe oryzae群体中AVR-Pia基因的分布及变异,利用水稻单基因系IRBLa-C水稻品种对自云南省13个市(州)采集分离得到的471株稻瘟病菌菌株进行抗性基因Pia有效性测定;利用无毒基因AVR-Pia特异性标记对471株稻瘟病菌菌株进行PCR检测和测序,并分析稻瘟病菌群体中无毒基因AVR-Pia的分布及DNA结构变异;利用有效性结果和PCR检测结果对471株菌株进行反应型划分,筛选鉴定菌株;利用鉴定菌株对云南省112份地方稻种进行Pia基因鉴定。结果表明,在471株稻瘟病菌菌株中,对含有Pia基因的水稻单基因系IRBLa-C表现为抗病和感病的菌株数分别为139株和332株,所占比例分别为29.5%和70.5%;在471株稻瘟病菌菌株中,分别有244株和227株菌株含有无毒基因AVR-Pia和不含有无毒基因AVR-Pia,所占比例分别为51.8%和48.2%,无毒基因AVR-Pia主要为完全缺失变异;在471株稻瘟病菌菌株中,A-和V+反应型菌株数分别为56株和161株,共217株,占总菌株数的46.1%,在13个市(州)稻瘟病菌群体中,A-和V+反应型菌株所占比例差异较大,其中在普洱市、红河哈尼族彝族自治州、昭通市、玉溪市4个市(州)的比例较大,分别为77.8%、57.1%、52.1%和50.0%;在112份云南省地方稻种质资源中,有20份地方稻品种含有抗性基因Pia,主要分布在9个市(州)中。表明云南省13个市(州)绝大部分水稻产区水稻Pia基因已丧抗性,含Pia基因的水稻种质在云南省分布较广。     

拟康宁木霉Tk1的分离鉴定、拮抗作用及其生物学特性

为了分离利用高效植物病害生物防治菌株,从广东药用植物金丝皇菊根部分离获得一株木霉菌株Tk1。经过形态观察、rDNA-ITS和EF-1α序列分析明确其为拟康宁木霉Trichoderma koningiopsis。用平板对峙培养法测定,该菌株对金丝皇菊枯萎病菌（尖孢镰刀菌Fusarium oxysporum）和柑橘炭疽病菌（胶胞炭疽菌Colletotrichum gloeosporioides）的抑制率分别为68.5%和77.1%,且在后期能完全覆盖或部分覆盖病原真菌。其无菌发酵液对金丝皇菊枯萎病菌的抑制率为45.55%。该菌株营养生长和产孢的最适碳源分别为乳糖和葡萄糖,最适氮源是酵母膏;在pH 4~11的培养基上均可生长、产孢,最适pH为7;12 h交替光照条件下菌丝的生长速度最快,全光照条件下产孢数量最大;该菌株的致死温度为73℃处理10 min。     

ROCK promotes high glucose-induced cardiomyocyte apoptosis by inhi-biting PI3K/Akt signaling pathway

AIMTo investigate whether Rho-associated coiled-coil kinase (ROCK) is involved in high glucose-induced apoptosis of primary cardiomyocytes by regulating PI3K/Akt signaling pathway. METHODSPrimary Wistar rat cardiomyocytes were cultured and identified by α-sarcomeric actin (α-SCA) immunohistochemistry. Cardiomyocytes were treated with 5.5, 33 and 40 mmol/L glucose for 48 h. The cell viability was measured by MTT assay, and the mRNA expression of ROCK1 and ROCK2 in the cardiomyocytes was detected by RT-qPCR. Flow cytometry was used to analyze the apoptosis of the cardiomyocytes. The protein levels of ROCK1, ROCK2, cleaved caspase-3, Bcl-2, PI3K, Akt and p-Akt were determined by Western blot. In order to confirm the regulatory effect of ROCKs on PI3K/Akt signaling pathway, the cells were divided into control group (5.5 mmol/L glucose), high glucose group (33 mmol/L glucose) and high glucose+Y27632 (ROCK inhibitor) group. Western blot was used to detect the protein levels of ROCK1, ROCK2, PI3K, Akt and p-Akt. RESULTSAfter 48 h of high glucose exposure, the values of relative cell viability in 33 and 40 mmol/L glucose groups were (79.71±2.43)% and (68.41±7.49)%, respectively, both of which were significantly decreased compared with normal control group (P<0.05). After 48 h of high glucose exposure, the relative mRNA levels of ROCK1 and ROCK2 in 33 and 40 mmol/L glucose groups were significantly increased compared with normal control group (P<0.05). Compared with normal control group, the apoptotic rate in 33 and 40 mmol/L glucose groups was increased significantly (P<0.05). Compared with normal control group, the protein expression of ROCK1, ROCK2 and cleaved caspase-3 in 33 and 40 mmol/L glucose groups was increased (P<0.05), while the protein expression of Bcl-2 was decreased (P<0.05). No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed, while the protein level of p-Akt in 33 and 40 mmol/L glucose groups was decreased compared with normal control group (P<0.05). Compared with high glucose group, the expression of ROCK1 and ROCK2 was decreased in high glucose+Y27632 group. No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed. Compared with normal control group, the protein level of p-Akt in high glucose group was decreased, and the protein level of p-Akt in high glucose+Y27632 group was increased significantly compared with high glucose group. CONCLUSION Under high glucose environment, ROCK may reduce the level of p-Akt by inhibiting the PI3K/Akt signaling pathway, thus promoting the apoptosis of cardiomyocytes.     

Effects of apelin-13 on oxidative stress induced by high uric acid in adipocytes

AIM: To study the effects of apelin-13 on oxidative stress induced by high uric acid in 3T3-L1 adipocytes and its underlying mechanisms. METHODS: 3T3-L1 adipocytes were stimulated with uric acid at 10 mg/dL for 48 h. Some of the adipocytes were administered with 1 μmol/L apelin-13 in the presence of uric acid at 10 mg/dL. The adipocytes stimulated with 100 μmol/L H₂O₂ were served as positive controls. The intracellular reactive oxygen species (ROS) concentrations were detected by flow cytometry. The biochemical kits were used to measure the activities of superotide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and NADPH oxidase (NOX) activity, and the content of malondialdehyde (MDA) in the cell lysate and the supernatant. The mRNA levels of renin-angiotensin system (RAS) components, including angiotensinogen (AGT), angiotensin-converting enzyrne1 (ACE1), angiotensin II type 1 receptor (AT1R) and AT2R, as well as angiotensin II receptor -like 1 (APJ) were measured by real-time PCR. The concentrations of angiotensin II (AngⅡ) in the cell lysate and the supernatant were measured by ELISA. RESULTS: Adipocytes stimulated with uric acid at 10 mg/dL had lower activities of antioxidant enzymes (SOD, GSH-PX and CAT) and higher levels of NOX activity and MDA content (P < 0.05). Accordingly, the intracellular ROS levels were found to be dramatically increased. However, apelin-13 administration attenuated uric acid-induced oxidative stress in the 3T3-L1 adipocytes. Uric acid at 10 mg/dL upregulated the mRNA expression of local RAS, enhanced AngⅡ concentrations both in the cell lysate and the supernatant, and down-regulated the mRNA level of APJ in the adipocytes (P < 0.05). Conversely, apelin-13 partially reversed these parameters. CONCLUSION: Apelin-13 attenuates oxidative stress induced by uric acid, may be via down-regulation of local RAS expression in the 3T3-L1 adipocytes.     

黄连中盐酸小檗碱的提取纯化及抑菌活性研究

为了探究盐酸小檗碱在植物病原真菌方面的抑制作用,以黄连根粉为材料,采用酸水法提取和乙醇重结晶获得盐酸小檗碱纯品,采用生长速率法研究了盐酸小檗碱对常见植物病原菌的抑制活性。结果表明,盐酸小檗碱的提取率为3.3%,经高效液相色谱法测得其含量为93.56%;抑菌活性试验表明,盐酸小檗碱在100μg/mL时对玉米大斑病菌的抑制率达99.9%,EC_(50)为8.20μg/mL,表现出比药剂对照噁霉灵和百菌清更高的抑制活性;进一步的试验表明,与噁霉灵及百菌清相比,盐酸小檗碱对玉米大斑病菌的抑制作用具有持效期长的特点。     

马铃薯组培苗时期不同LED光源处理对温室移栽后植株生长和微型薯结薯的影响

不同LED光源下培养的马铃薯组培苗在形态特征上差异明显,为探索这种差异是否会对其移栽后产生进一步影响,试验研究了100%红光(R)、100%蓝光(B)、100%绿光(G)、75%红光+25%蓝光(RB)、45%红光+35%蓝光+20%绿光(RBG)和100%白光(CK)6种光谱下培养4周的马铃薯组培苗温室移栽后植株的生长和结薯情况。试验结果表明,B处理的马铃薯组培苗移栽后缓苗期叶绿素荧光参数Fv/Fm和qP、结薯前期SPAD值及结薯期各器官生物量均始终高于CK和其他处理,且该处理下最大薯的干鲜重和有效微型薯占比分别较CK提高45.66%、45.09%和10.93%。R处理的组培苗移栽后结薯期地上部生物量显著高于CK,单株结薯数目提高29.60%,但有效微型薯占比较CK降低63.97%。G处理的组培苗移栽后生长和结薯指标均表现最差。组合光谱RB和RBG处理的组培苗移栽后的生长指标和微型薯产量及产量构成指标均与CK无显著差异。因此,单色红、蓝、绿光谱处理对马铃薯组培苗的影响会持续至其移栽后植株幼苗生长,甚至结薯期,组合光谱RB和RBG则不会。在马铃薯组培苗生产上,单色蓝光和单色红光作为照明光源具有潜在的应用价值,组合光谱RB和RBG可作为白色光源的替代光源。     

基于无人机多光谱遥感的冬小麦叶绿素含量反演及监测

旨在实现冬小麦各生育期叶绿素含量的准确估测,探究其时空变化规律。利用无人机获取冬小麦越冬期、返青期、拔节期、孕穗期和灌浆期的高分辨率多光谱图像,同时采集地面SPAD数据。选取三类光谱参数建立反演模型,优选出各生育期的最佳预测模型,并定量监测试验区冬小麦叶绿素含量时间变化和空间分布。结果表明：原始波段模型和波段倒数对数模型分别为越冬期及其他生育期叶绿素含量预测的最佳模型,拟合精度R²>0.59;时空分布上,灌浆期前试验区冬小麦叶绿素含量呈南北高、中部低特点,灌浆期则呈北高南低的趋势,叶绿素含量从越冬期到拔节期逐步增加,拔节期到孕穗期开始降低,孕穗期到灌浆期则大幅度降低。本研究建立的倒数对数预测模型,精度较高,且适用于返青到灌浆的4个生育期,对于试验区冬小麦叶绿素含量有较好的时空监测效果。