黑龙江省水稻产业现状分析及未来发展思路

对黑龙江省水稻产业发展现状进行了小结,并针对黑龙江省水稻生产过程中存在问题提出了相应的对策。具体对策如下:有针对性的选育适于不同生态区域的优质、抗逆水稻新品种,并对新品种的轻简高效配套栽培技术进行研究;适时开展水稻直播关键技术集成与应用,及开展秸秆还田技术研究;开展稻米精加工技术研究。     

基于称重式蒸渗仪的淮北平原冬小麦蒸散估算模型的本地化

为了解不同作物蒸散量估算方法在淮北地区的适用性,利用新马桥实验站称重式蒸渗仪测定了2016-2017年冬小麦全生育期的实际蒸散值,结合Hargreaves-Samani(H-S)、 FAO-56 PM、Turc、Makkind(Mak)、 Priestley-Taylor(P-T)、Mcloud(Mcl)和DeBruin-Keijman(D-K)7个模型,分析了冬小麦田的蒸散特征,将蒸散的估算值(ET_0)和实测值(ET_C)进行了对比。结果表明,相对于ET_C值,7个模型拟合得到的ET_0的RMSE值为0.99～2.29 mm·d~(-1),且H-S FAO-56 PMTurcMakP-TMclD-K; ET_C与ET_0的相关系数为0.74～0.97,其中FAO-56 PM的相关性最高,P-T、 Mak、 D-K、 H-S也表现出较好的相关性。综合来看,H-S法总体表现较好,更适合该地区。对6种主要气象要素与实测蒸散值进行主成分分析发现,温度是影响ET_C的主要因子,湿度、日照时数和平均风速(2 m)对淮北冬小麦田蒸散值的影响不大;H-S模型以温度数据为基础,利用线性订正法和湿度指数项订正法将H-S模型本地化后检验发现,其优化结果良好,RMSE降低(0.68 mm·d~(-1))。     

玉米脱粒破碎率关键影响因子及其最优预测模型研究

子粒破碎率高是当前中国玉米机械收获子粒的重要限制因素,解析破碎率变化原因,建立其简便预测模型是需要解决的重要问题。本文采集7个玉米品种在3个种植密度下组合的果穗,在不同子粒含水率梯度条件下开展单穗脱粒试验。种植密度在6万～9万株/hm2范围内对子粒破碎率没有影响,品种、子粒的含水率、抗侧压碎力和穿刺强度等的影响均达到统计显著水平。品种对破碎率变化的偏贡献率为12.7%,且品种的偏贡献率子粒含水率的偏贡献率抗侧压碎力的偏贡献率穿刺强度的偏贡献率,种植密度的偏贡献率接近于零。破碎率的最优预测因子是穿刺强度,预测模型:破碎率=10.25×0.990穿刺强度,满足破碎率不高于5%约束的穿刺强度值不得低于60 MPa。研究结果可为玉米破碎率预测、宜机收玉米新品种培育与鉴定、脱粒机具设计与制造提供数据支撑和技术参考。     

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 calpain-2 and autophagy-related protein 5 on hepatocyte apoptosis induced by endoplasmic reticulum stress

AIMTo investigate the effects of calpain-2 and autophagy-related protein 5 (Atg5) on apoptosis of BRL-3A rat normal liver cells during endoplasmic reticulum stress (ERS) induced by dithiothreitol (DTT). METH?ODS: BRL-3A cells were treated with DTT at 2.0 mmol/L for 0, 6, 12 and 24 h to induce ERS. Real-time cell analysis (RTCA) was used to measure the effect of DTT on BRL-3A cell proliferation. Apoptosis and cell cycle distribution were analyzed by flow cytometry. The mRNA expression of calpain-2 and Atg5 was detected by real-time PCR. The protein levels of calpain-2, Atg5, Atg7, Atg12 and microtubule-associated protein 1 light chain 3 (LC3) were determined by Western blot. The interaction between calpain-2 and Atg5 was investigated by co-immunoprecipitation (Co-IP). RESULTSThe proliferation of BRL-3A cells treated with DTT was significantly inhibited. The apoptosis of BRL-3A cells was significantly increased after DTT treatment for 6, 12 and 24 h as compared with 0 h group (P<0.05). The cell cycle was arrested in G₁ phase after DTT treatment (P<0.05). After DTT treatment for 6, 12 and 24 h, the mRNA expression of calpain-2 and Atg5 in the BRL-3A cells was significantly increased as compared with 0 h group (P<0.05). The protein levels of calpain-2, Atg12 and Atg7 in the cells treated with DTT for 6, 12 and 24 h were significantly higher than those in 0 h group, and the ratio of LC3-II/LC3-I was also significantly higher than that in 0 h group, while Atg5 expression was significantly lower than that in 0 h group (P<0.05). The results of Co-IP found that the anti-calpain-2 antibody precipitated Atg5 protein from the cell lysates, and the anti-Atg5 antibody also precipitated calpain-2 from the cell lysates, which confirmed the interaction between calpain-2 and Atg5. CONCLUSION Calpain-2 may participate in ERS-induced hepatocyte apoptosis by interacting with Atg5.     

卷丹转基因体系构建及岷江百合LrCCoAOMT的导入

以卷丹（Lilium lancifolium Thunb.）无菌小鳞片为试材,通过切片处理、优化农杆菌侵染浓度与时间以及重悬液和共培养基成分,构建农杆菌介导的高效遗传转化体系。结果表明,MS + 1.5 mg ? L-1 6-BA + 0.5 mg ? L-1 NAA + 30 g ? L-1蔗糖是切片芽分化的最佳培养基,添加100 mg ? L-1抗坏血酸能有效抑制褐化并促进不定芽增殖。MS + 2.0 mg ? L-1 NAA + 30 g ? L-1蔗糖是生根诱导的最佳培养基。抗生素敏感性测试发现,培养基中添加Kan 100 mg ? L-1或Hyg 75 mg ? L-1 结合Cef 400 mg ? L-1适宜抗性筛选。GUS染色分析表明,以去除大量元素的改良MS + 100 μmol ? L-1 AS和去除大量元素的改良MS + 1.0 mg ? L-1 6-BA + 1.0 mg ? L-1 NAA + 100 μmol ? L-1 AS为重悬液和共培养基,将切片在农杆菌菌液浓度OD600为0.4,侵染15 min,获得81.72% 瞬时转化率和25.2% 稳定遗传转化率。将岷江百合LrCCoAOMT转化卷丹,分子检测和GUS染色分析表明已获得转基因阳性株系。     

枸杞Lb_PPR1的克隆及其在不同育性品种中的表达分析

三角状五肽重复（Pentatricopeptide repeats,PPR）蛋白定位于多种细胞器中,参与细胞核和细胞器中特异单链RNA的转录后修饰和编辑,在植物生长发育的多个阶段均发挥着重要的作用。分别从枸杞（Lycium barbarum）雄性可育系‘宁杞1号’和不育系‘宁杞5号’中克隆了Lb_PPR1基因,并对其编码蛋白质进行理化性质、亚细胞定位、保守结构域、蛋白结构以及系统进化等方面进行预测分析。结果显示,‘宁杞1号’和‘宁杞5号’中Lb_PPR1基因的开放阅读框均为1 977 bp,编码658个氨基酸,但其中存在20个碱基和14个氨基酸的差异。Lb_PPR1蛋白包含14个串联重复的PPR保守基序,属于PLS家族,该蛋白定位在细胞膜和细胞质。二级、三级结构预测显示该蛋白以α螺旋为主。同源进化分析得出Lb_PPR1蛋白与同属茄科的辣椒和烟草PPR蛋白亲缘关系最近。利用实时荧光定量PCR检测Lb_PPR1在枸杞不同组织器官及不同发育阶段花药中的表达特性。结果显示,Lb_PPR1在枸杞不同组织中均有表达,但在可育系花蕾中表达量最高,不育系‘宁杞5号’各组织中表达量均显著低于可育系‘宁杞1号’。以上结果表明,Lb_PPR1基因可能与枸杞花药发育有关。     

四川地区猕猴桃病毒1的RT-PCR检测及外壳蛋白基因序列分析

为了明确近期新西兰报道的侵染猕猴桃的新病毒——猕猴桃病毒1（Actinidia virus 1,AcV-1）在四川地区猕猴桃上的发生情况及其分子特性,采用RT-PCR对来自四川6个地区疑似感染病毒的90份猕猴桃主栽品种‘红阳’和‘金果’的叶片样品进行检测。结果表明,22份样品为AcV-1阳性,检出率为24.4%。将获得的5个AcV-1分离物和已报道的新西兰分离物K75的外壳蛋白（coat protein,CP）基因序列进行比对,结果表明,分离物间核苷酸序列和氨基酸序列的相似性分别为84.8% ~ 97.1%和89.7% ~ 99.6%,其中除邛崃分离物HYH5与新西兰分离物K75的核苷酸序列相似性较高（97.1%）外,其余4个分离物均低于91%。系统进化分析结果显示,这些分离物主要聚集在3个分支上,分离物HYH5与新西兰分离物K75位于同一分支,其余分离物位于另外2个分支。