高产抗逆大豆新品种石豆12号的选育     

牛宁  金素娟  赵璇  付雅丽  王玉岭  李占军 《大豆科学》2017,36(4)

石豆12号是由石家庄市农林科学研究院以石豆1号为母本,汾豆63为父本经有性杂交选育而成。2015-2016年参加河北省夏播大豆区域试验,平均产量3 284.0 kg·hm~(-2),较对照冀豆12增产6.22%。2016年参加河北省夏播大豆生产试验,平均产量3 229.7 kg·hm~(-2),较对照冀豆12增产4.91%。2017年通过河北省农作物品种审定委员会审定,准予推广。石豆12号的主要特点是高产、抗病、抗倒伏,适宜在河北省中南部夏播种植。  相似文献   

玉米大斑病菌StSte12基因对H_2O_2氧化胁迫的应激调节     

张运峰 《玉米科学》2017,25(4):144-149

通过比较野生型菌株Wt01-23与StSte12基因RNAi沉默突变体菌株StRNAi9-10和StRNAi3-6在H_2O_2胁迫下生长和发育方面的差异,分析转录因子基因StSte12对玉米大斑病菌氧化胁迫的调节能力。在不同浓度H_2O_2胁迫条件下,测定野生型菌株和突变体菌株的菌落生长速度、菌丝形态、产孢量和菌丝萌发率。结果表明,随着H_2O_2浓度的增加,玉米大斑病菌野生型菌株和突变体菌株的菌落生长速度、产孢量和菌丝萌发率均显著降低,但突变体菌株的降低程度显著高于野生型菌株,表明StSte12基因对玉米大斑病菌的氧化应激调节具有重要的调控功能。  相似文献   

籼粳杂交稻甬优12百亩方13.50 t/hm~2高产栽培技术     

占才水  周昌南  章秀福 《中国稻米》2017,(6):88-89

籼粳杂交稻甬优12具有株型优良、穗大粒多、结实率高、高产稳产、优质多抗等特点。2013-2016年在浙江省江山市进行百亩方攻关试验,2016年创造了单产14.56 t/hm~2的浙江省单季稻攻关田历史最高纪录。本文介绍了甬优12的特征特性,并详细阐述了甬优12百亩攻关方单产达13.50 t/hm~2的高产栽培技术。  相似文献   

“高粱+再生高粱”高产高效栽培技术研究   总被引：2，自引：0，他引：2  

范昭能  曾荣耀  杨航  何丽平  童小兰 《中国农学通报》2017,33(12):24-29

为提高高粱在"种植一季有余、两季不足"的温光资源条件下的种植效益,以‘泸糯12号’为研究材料,通过优化播期、促芽肥等关键技术研制"高粱+再生高粱"高产高效栽培技术,再与传统技术进行对比试验。结果表明,"高粱+再生高粱"高产高效栽培技术要点是2月底至3月5日前播种,种植密度101055株/hm~2,头季高粱收获前10天及时施纯氮150 kg/hm~2,留桩高度控制在近地面第1节位,每窝保留再生苗2~3苗。应用"高粱+再生高粱"高产高效栽培技术后两季高粱产量和效益,较传统高粱种植技术分别增长120.3%、84.3%,增产增效效果显著。因此,"高粱+再生高粱"高产高效栽培技术适宜区域大面积推广。  相似文献   

Role of ghrelin in cell protection by up-regulating HSP70 through ERK1/2 signaling pathway in PC12 cells     

SHI Ting  SONG Wei-fang  SUN Chang-wei  ZHU Shi-gong 《园艺学报》2019,35(6):1095-1100

AIM:To study the role of ghrelin in cell protection by up-regulating heat shock protein 70 (HSP70) and inhibiting apoptosis induced by oxidative stress through extracellular regulated protein kinases 1/2 (ERK1/2) signaling pathway in the PC12 cells. METHODS:Sodium nitoprusside (SNP) was used to induce oxidative stress injury in the PC12 cells. The cultured PC12 cells were divided into SNP-injured group (incubated with SNP at 0.5 mmol/L for 6, 12, 18 and 24 h), ghrelin pretreatment group (ghrelin at 100 nmol/L was given 30 min before adding SNP); HSP70 inhibitor group (quercetin at 10 μmol/L was added 60 min before ghrelin treatment), ERK inhibitor group (ERK 1/2 inhibitor PD98059 was added 60 min before ghrelin treatment) and control group (added same amount of culture medium only). The apoptotic rate was detected by flow cytometry. The protein expression was determined by Western blot and immunocytochemistry. RESULTS:Compared with control group, the apoptotic rate of PC12 cells in SNP-injured group was significantly increased (P<0.05). Compared with SNP-injured group, ghrelin (100 nmol/L) pretreatment significantly inhibited SNP-induced apoptosis of PC12 cells (P<0.05), and significantly up-regulated the protein expression of HSP70 (P<0.05). Time-effect analysis showed that ghrelin had the most significant effect at 18 h after SNP injury. Quercetin, an inhibitor of HSP 70, significantly reduced the anti-apoptotic effect of ghrelin (P<0.05). Ghrelin pretreatment promoted the phosphorylation of ERK1/2. ERK1/2 inhibitor PD98059 significantly inhibited the effects of ghrelin on up-regulation of HSP70 expression (P<0.05). CONCLUSION:Ghrelin upregulates the expression of HSP70 and inhibits the apoptosis in the PC12 cells induced by oxidative stress by promoting the phosphorylation of ERK1/2.  相似文献   

Effects of DHRS3 in C2C12 Myoblast Differentiation and Mouse Skeletal Muscle Injury     

Zhang Wen-yu  Xu Jia-hui  Zhang Chun-yu  Tong Hui-li  Li Shu-feng  Yan Yun-qin 《东北农业大学学报(英文版)》2021,28(3):38-47

Myoblast differentiation is an essential process during skeletal muscle development. C2 C12 myoblast is a commonly used experimental model to study muscle cell differentiation in vitro. Dehydrogenase/reductase(SDR family) member 3(DHRS3) is a highly conserved member in short-chain alcohol dehydrogenase/reductase superfamily and has been shown to be involved in the metabolism of retinol. Previous experimental results showed that the expression of DHRS3 increased significantly during the differentiation of myoblasts differentiation. However, the effect of DHRS3 on mouse muscle cell differentiation was unclear. The objective of current study was to determine if DHRS3 affected muscle cell differentiation, and if DHRS3 was involved in muscle regeneration. Protein expression was determined by western blot and immunofluorescence analysis. The activation and inhibition of DHRS3 increased and decreased C2 C12 myoblast differentiation respectively, which indicated that DHRS3 could affect C2 C12 myoblast differentiation. DHRS3 expression was significantly changed during muscle regeneration, with the regeneration of muscle injury, the expression of DHRS3 tended to increase first and then decrease. It suggested that DHRS3 might be involved in muscle regeneration. In summary, this study confirmed the involvement of DHRS3 in C2 C12 myoblast differentiation and mouse skeletal muscle regeneration and provided a theoretical basis for further elucidating the molecular mechanism of muscle development.  相似文献   

Tillage effects on soil organic matter in density fractions of a Cerrado Oxisol   总被引：15，自引：0，他引：15  

R. Roscoe  P. Buurman 《Soil & Tillage Research》2003,70(2):107-119

Reclamation of Brazilian cerrados (savannas) has been intensified in the last decades, with implications for soil quality and soil organic matter (SOM) dynamics. Studying the impact of different tillage systems is essential to define better strategies for land use in Cerrado, which may favor C sequestration and improve soil quality. We used density fractionation and ¹³C natural abundance to assess changes in SOM in an Oxisol previously under a cerrado sensu-stricto following 30 years of cultivation. The objectives of the study were to: (i) evaluate the long-term impact of tillage systems on SOM stocks in a Dark Red Latosol (Oxisol) from the Cerrado Biome, and (ii) better understand the dynamics of SOM in different density fractions of this soil. Cultivation led to compaction, which significantly increased soil bulk density. This resulted in the systematic overestimation of C and N stocks in cultivated areas when compared to the natural cerrado. Conversion of the cerrado into cropland using plow tillage (PT) or no-tillage (NT) system did not alter the total C (100 Mg ha^"12;1) and N (7 Mg ha^"12;1) stocks in the first 45 cm depth at the end of 30 years of cultivation. However, about 22% of the total C was replaced by C from maize. The relative replacement of C decreased following the order: free light fraction (F-LF)>heavy fraction (HF)>occluded light fraction (O-LF). The low substitution in the O-LF was attributed to a possible presence of charcoal. Converting cerrado into cropland significantly decreased F-LF quantity. The proportions of C replacement in this fraction were higher in PT than NT, suggesting a faster turnover in PT. Nevertheless, because most C (95%) was held in the HF, C dynamics in the whole soil were controlled by the behavior of this fraction. The maintenance of C levels even at the end of 30 years of cultivation and the lack of differentiation between NT and PT were attributed to the high clay contents and Fe+Al oxi-hydroxides concentrations of the studied soil as well as to a sufficient C supply by the maize crop.  相似文献   

2个桉树无性系微量元素叶片营养诊断初探   总被引：2，自引：0，他引：2  

李淑仪  蓝佩玲  廖新荣  杨国清  简明  徐胜光 《浙江林学院学报》2005,22(1):40-45

为了进一步提高桉树Eucalyptus产量,对桉树施微肥试验区的叶片进行了分析.采用叶片营养诊断临界值法探讨了2个桉树无性系的微量元素营养状况,初步获得了刚果12W5桉E.ABL 12W5和尾叶桉U6E. urophylla U6的部分微量元素营养的诊断指标,并进一步在中试区作诊断评价和检验.结果表明:桉树叶片的钼、锌、铜、锰的质量分数与一般植物的有差异.2个无性系的微量元素叶片营养诊断临界值,刚果12W5桉为硼27.90 mg·kg-1 ,锌45.00 mg·kg-1 ,铜1.08 mg·kg-1 ,铁288.00 mg·kg-1 ;尾叶桉U6为:硼13.50 mg·kg-1 ,锌10.80 mg·kg-1 ,钼0.15 mg·kg-1 ,锰216.00 mg·kg-1 ,铁117.00 mg·kg-1 ,其中桉树叶片养分诊断标准与微肥中试区的叶片分析数据相吻合的有这2种桉树叶片中的硼,尾叶桉中的钼,刚果桉中的铜;而中试区的桉树叶片锌、铁、锰的分析数据均未能与诊断标准相吻合,故这3种元素暂不适宜用临界值法诊断指导施肥.表6参22  相似文献   

芝麻新品种中芝12配套栽培技术研究   总被引：1，自引：0，他引：1  

赵应忠  刘红艳  高广金  黄开意  苏元清 《湖北农业科学》2006,45(3):307-309,313

在湖北鄂州和武汉进行了芝麻新品种中芝12的播期、密度、打顶、化控及高产攻关试验,结果表明,该品种的最适宜播期为5月30日,密度为每公顷15万株,第3对真叶期间隔1周连喷两次150mg·kg-1或200 mg·kg-1缩节胺.中芝12在高肥水条件下不宜打顶,但在一般种植条件下以初花后25 d打顶效果好.鄂州和武汉高产攻关公顷产量分别为2 139.75kg 和2 418.75kg.  相似文献   

水貂12S rRNA基因的克隆     

王红梅  白秀娟 《经济动物学报》2006,10(4):193-195

为探讨水貂的系统发育关系,对金州水貂的12S rRNA基因进行了克隆测序,序列长度为450 bp。结果表明,金洲水貂的12S rRNA基因与伶釉的同源性为92.48%,与林釉的同源性为91.83%,与北美水貂的同源性为90.99%,与獾的同源性为90.99%。  相似文献