新疆生产建设兵团第四师71团玉米密植高产全程机械化生产技术模式发展调研

从种植品种、种植密度与种植方式、机械化作业和收储烘干等环节对新疆生产建设兵团第四师71团场玉米生产技术的发展进行调研。分析表明,71团场位于西北灌溉玉米区,通过规模化、标准化生产和统一作业管理,以密植增产为基础、子粒收获为核心、绿色防控与秸秆还田为保障构建的玉米密植高产全程机械化绿色生产技术,实现了高产和高效的协同提高与绿色可持续生产。经农业农村部专家指导组田间测产验收,2012年、2014年和2017年连续创造16701 kg/hm^2、18414 kg/hm^2和18447 kg/hm^2的全国玉米大面积(700 hm^2)高产纪录,净利润在15000元/hm^2以上,为现代玉米生产树立了成功的模式和样板。     

不同氮肥处理下高温胁迫对夏玉米产量及叶片超微构造的影响

以郑单958为材料,研究高温胁迫对夏玉米产量及叶片超微构造的影响。结果表明,高温处理缩短夏玉米的生育天数,降低夏玉米产量及叶绿素含量。随氮肥增加,高温处理对玉米产量的影响先降低后升高(在310.5 kg/hm^2氮肥下,高温处理玉米产量的降低达到27.2%、31.1%)。高温处理较对照维管束鞘细胞变大,高温处理维管束鞘细胞内的叶绿体出现淀粉粒,对照处理维管束鞘细胞内的叶绿体没有出现淀粉粒。高温线粒体及细胞核(被)膜开始解离,对照处理线粒体及细胞核(被)膜完整,说明高温条件下,玉米对氮的耐受力降低。高温处理叶绿体数、叶绿体基粒数减少及基粒片层数减少,叶绿体面积及叶绿体长/宽比值变小,高温处理较对照线粒体数先增加后减少。高温处理与对照叶肉细胞叶绿体内均未发现淀粉粒。     

河北省玉米小斑病菌优势生理小种鉴定及ITS序列分析

2007~2016年在河北各地采集玉米小斑病标样,对分离出的356株玉米小斑病菌菌株进行生理小种鉴定。结果表明,在鉴定的年度范围内,玉米小斑病菌T小种、C小种、S生理型、O小种的分离频率在年度间存有差异,O小种的平均分离频率94.94%,是河北省玉米小斑病菌的优势小种;O小种对主栽品种郑单958和自交系C103的致病力呈下降趋势,在C103上致病力下降幅度小于郑单958。对河北省石家庄、保定、衡水、沧州邯郸、邢台采集的45株菌株进行ITS序列分析构建UPGMA进化树,分析表明,河北省内玉米小斑病菌株的遗传进化与地域有一定关系,差异不明显。     

灌水对强筋小麦籽粒产量及营养品质的影响

为明确水地强筋冬小麦高产、优质、高效的灌溉技术,试验设3个灌水时期8个灌溉处理［越冬期灌1水（W₁）,拔节期灌1水（W₂）,孕穗期灌1水（W₃）,越冬期和拔节期灌2水（W₁₂）,越冬期和孕穗期灌2水（W₁₃）,拔节期和孕穗期灌2水（W₂₃）,越冬期、拔节期和孕穗期灌3水（W₁₂3）,全生育期不灌水处理（CK）］,于小麦成熟期测定籽粒产量、总蛋白及其组分含量和淀粉含量。结果表明,与不灌水的CK比较,所有灌水处理的籽粒产量、有效穗数、穗粒数、千粒重、蛋白质产量以及籽粒淀粉含量均显著增加,但籽粒的总蛋白及其组分含量均呈不同程度降低（W₁处理除外）。越冬期灌水对有效穗数、籽粒产量、总蛋白及其组分含量、淀粉含量的提升作用较大;拔节期灌水对穗粒数的提升作用较大,但对淀粉含量的提升作用较小,对总蛋白及其组分含量的降低作用较大;孕穗期灌水对千粒重的提升作用较大,对蛋白质产量的提升作用较小。随着灌水次数增加,小麦籽粒产量显著提高,淀粉含量先显著提高后基本不变,而籽粒总蛋白及其组分含量降低。W₁₂3处理籽粒产量最高,其次是W₁₃处理;W₁处理籽粒蛋白质及其组分含量最高,其次是W₁₂及W₁₃处理;W₂₃处理淀粉含量最高,其次是W₁₂或W₁₃处理。综合各项指标,最好的灌水组合是越冬期和孕穗期灌2水（W₁₃）。     

春季低温对小麦颖果发育的影响

为了探明春季低温（倒春寒）导致小麦减产的细胞学机理,以扬麦15为材料,在小麦幼穗处于雌雄蕊分化期至药隔期之间时,设置-3 ℃低温处理,通过树脂半薄切片对颖果不同发育时期的形态结构进行观察。结果表明：（1）在颖果发育早期,低温促进了颖果的长度生长,抑制了宽度生长;与对照相比,低温处理组小麦颖果发育进程缩短;（2）低温处理组颖果果皮发育早,中果皮降解速度快;（3）低温处理增加了胚乳淀粉体的积累量,降低了蛋白体的积累量,发育后期胚乳充实度显著低于对照组;（4）与对照相比,低温处理后颖果韧皮部面积和珠心突起传递细胞面积增大。以上结果表明,春季低温处理更有利于养分运输组织的发育,使得灌浆时间缩短,最终导致淀粉积累量增加及颖果早熟。     

外源褪黑素和脱落酸对干旱胁迫下葡萄生理特性的影响

为了探讨褪黑素(MT)和脱落酸(ABA)两者混合施用对植物响应干旱胁迫的综合效应,以盆栽‘阳光玫瑰’葡萄为材料,通过根灌100μmol·L~(-1)的MT溶液和叶面喷施50μmol·L~(-1)的ABA溶液及二者组合处理,研究MT和ABA对干旱胁迫下葡萄生理特性的影响。结果表明,与干旱对照组(D_(ck))相比,MT处理导致葡萄叶片MDA、H_2O_2含量和相对电导率分别降低了14.42%、44.11%和21.26%,叶片相对含水量提高了1.12%,同时SOD和POD酶活性分别提高了14.00%和3.01%。这些均表明MT处理有效缓解了干旱胁迫对植株造成的损伤。50μmol·L~(-1 )的ABA处理组叶片MDA含量和相对电导率较干旱对照组提高了9.43%和17.25%,表明ABA处理没有缓解植株的胁迫状态。MT和ABA组合处理具有和MT处理类似的效果。结果表明,褪黑素可以通过减轻膜脂过氧化程度,增强抗氧化系统能力,从而缓解干旱胁迫对葡萄的氧化损伤,提高抗旱性;同时削弱ABA带来的负面效应。     

CD36/Src/ERK pathway is involved in process of monocyte differentiation into macrophages

AIM To investigate the role of fatty acid translocase (FAT/CD36) on differentiation of monocytes to macrophages. METHODS Human monocyte THP-1 cells were treated with phorbol 12-myristate 13-acetate (PMA) at 0, 100 and 200 μg /L. Small interfering RNA (siRNA) targeting CD36 (siCD36) was employed to knock down the expression of CD36 in THP-1 cells. The CD36 over-expression (CD36OE) cell line was constructed by transfection with a recombinant lentivirus containing CD36 cDNA. Optical microscopy and crystal violet staining were used to detect the monocyte morphological changes and adhesion ability. The protein expression of CD36 was measured by flow cytometry and Western blot. The mRNA levels of CD36, CD11b and CD80 were detected by real-time PCR. The protein levels of extracellular signal-regulated kinase (ERK） and Src tyrosine kinase were determined by Western blot. RESULTS The cellular adhesiveness of THP-1 cells was elevated in the process of monocytes differentiation, and the expression of CD36 was increased in this process as well (P<0.01). siCD36 was transfected into the THP-1 cells (CD36i group) and the silencing efficiency was approximately 80%. The cell surface area and cellular adhesiveness were significantly decreased in CD36i group compared with scrambled siRNA (NCi) group (P<0.01). The mRNA levels of CD11b and CD80 were decreased in CD36i group compared with NCi group (P<0.01). The cell surface area and cellular adhesiveness were increased in CD36OE group compared with empty vector (vector) group (P<0.05). The mRNA levels of CD11b and CD80 were increased in CD36OE group compared with vector group (P<0.01). The phosphorylation levels of ERK and Src were decreased in CD36i group compared with NCi group (P<0.05). CONCLUSION CD36 promotes the differentiation of human monocyte THP-1 cells to macrophages by increasing the phosphorylation of Src and further activating ERK.     

Panax notoginseng saponins suppress oxygen-glucose deprivation/reoxygenation-induced pyroptosis of SH-SY5Y cells

AIM To investigate the effect of Panax notoginseng saponins (PNS) on pyroptosis of SH-SY5Y cells induced by oxygen-glucose deprivation/reoxygenation (OGD/R). METHODS The OGD/R was conducted to induce ischemia/reperfusion injury in SH-SY5Y cells. The effects of PNS on the viability (detected by CCK-8 assay) and membrane permeability [indicated by lactate dehydrogenase (LDH) leakage and propidium iodide (PI) staining positive cell proportion] of OGD/R-induced SH-SY5Y cells were observed. The protein levels of gasdermin D (GSDMD), GSDMD N-terminal fragment (GSDMD-N), caspase-1 and caspase-4, and the release of interleukin-1β (IL-1β) and IL-18 in the cells were also determined. RESULTS After exposure to OGD/R, the viability of SH-SY5Y cells dramatically decreased (P<0.01), while the LDH leakage, the PI staining positive cell proportion, the protein levels of GSDMD, GSDMD-N, caspase-1 and caspase-4, and the release of IL-1β and IL-18 were significantly increased (P<0.01). However, PNS treatment enhanced the viability of SH-SY5Y cells inhibited by OGD/R (P<0.01), but reduced the leakage of LDH and the percentage of PI staining positive cells (P<0.05 or P<0.01). Moreover, PNS reversed the increases in the protein levels of GSDMD, GSDMD-N, caspase-1 and caspase-4 and the release of IL-1β and IL-18 in OGD/R-induced SH-SY5Y cells (P<0.05 or P<0.01). CONCLUSION Treatment with PNS alleviates OGD/R-induced injury in SH-SY5Y cells. Its mechanism may be related to inhibition of SH-SY5Y cell pyroptosis induced by OGD/R.     

大粒板栗新品种‘秦栗2号’

（西北农林科技大学林学院,陕西杨凌 712100）     

具有III型分泌系统的Pseudomonas moraviensis FP1761植物益生功能及其全基因组分析

 本研究从节瓜根际分离到一株具有防病促生功能的荧光类假单胞菌FP1761。该菌株对部分植物病原真菌和细菌具有拮抗能力,能够解钾、解有机磷和无机磷,可产生氨、蛋白酶、嗜铁素、吲哚乙酸。生物测定表明菌株FP1761可显著促进小麦生长。生理生化、平均核苷酸相似度、16S rDNA和多基因分析将FP1761鉴定为摩拉维亚假单胞菌(Pseudomonas moraviensis)。菌株FP1761基因组草图全长6.12 Mb,(G+C)含量为59.9%,共编码5467个基因序列。将该菌株与种内3个代表性菌株进行泛基因组和核心基因组分析,共产生 4 357个共有基因,菌株FP1761特有基因327个。利用antiSMASH对菌株次生代谢基因簇进行预测,发现其含有8个潜在的次生代谢产物基因簇。其中两个基因簇与嗜铁素pyoverdine合成相关,未见聚酮类合成基因。基因组分析发现,该菌株具有与病原性假单胞菌相似的III型分泌系统,但丢失了效应蛋白调控因子hrpS和转运相关的hrpH和hrpK1基因。对全基因组扫描,菌株FP1761仅保留了病原性假单胞菌的保守效应蛋白AvrE和HopAA1-1。FP1761是目前已发现的唯一具有III型分泌系统的摩拉维亚假单胞菌。本研究表明摩拉维亚假单胞菌FP1761具有潜在的植物防病促生功能,但其III型分泌系统与植物益生互作机制有待进一步解析。