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1.
The cyclic hexadepsipeptide enniatin is known as a phytopathogenic compound from Fusaria causing necrosis and wilt. The molecule consists of three alternating residues each of a branched chain amino acid and D-hydroxyisovaleric acid (D-Hiv). Enniatins are synthesized by a 347kDa multienzyme (enniatin synthetase) via a thiol template mechanism. The corresponding gene esyn1 has an open reading frame of 9393 nucleotides and harbours two modules, one responsible for D-hydroxy acid activation and one for L-amino acid activation with an integrated N-methyltransferase domain. Such methyltransferases build an homologous group among N-methyl peptide synthetases. Enniatins are synthesized by step-wise condensation of dipeptidol building blocks in an iterative manner resembling fatty acid synthesis. A key enzyme in enniatin biosynthesis is the NADPH-dependent D-2-hydroxyisovalerate dehydrogenase, that supplies enniatin synthetase with D-Hiv. Enniatins contribute to the wilt toxic character of Fusaria. Virulence was significantly reduced in F. avenaceum after disruption of the esyn1 gene.  相似文献   
2.
Bovine isoleucyl-tRNA synthetase (IARS) disorder, a major cause of weak calf syndrome, is caused by a homozygous missense (c.235G>C) mutation in the bovine IARS gene of Japanese Black (JB) cattle, which was identified in 2013. However, the extent to which the carrier rate has changed at Kagoshima prefecture, Japan, and whether the carrier status is associated with any clinical or reproductive problems, have yet to be ascertained. In this study, using a real-time polymerase chain reaction-based genotyping assay, we determined the carrier rate in a regional JB cow population at Kagoshima prefecture. Comparative analyses were performed on the metabolic profile test (MPT) results and reproductive performance data obtained for heterozygous carrier and homozygous wild-type cows. In 2009 and 2018, DNA samples were collected from 130 and 462 clinically healthy JB cows, respectively, in Kagoshima prefecture. MPT results and reproductive performance data were evaluated for 62 cows, comprising four heterozygous carriers and 58 wild-type cows. Genotyping revealed that the carrier rate was 6.9% in 2009 and 1.5% in 2018, the difference of which was statistically significant (P<0.005). There were no statistically significant differences between the carrier and wild-type cows with respect to either MPT results or reproductive performance, indicating that the carrier cows have necessary IARS activity to maintain minimal health and reproductive potential.  相似文献   
3.
The objective of this experiment was to evaluate the effects of dietary glutamine and glucose on pectoralis major meat quality in broilers under acute heat stress. Three hundred 35-day-old male broilers (Arbor Acres) were randomly divided into 5 groups. Broilers in the positive control group were kept in a thermoneutral environment (23 ± 1°C, RH 45%–55%) and fed a basic diet, whereas the experimental (2 × 2) group was exposed to acute heat stress (34 ± 1°C, RH 65%–75%) for 12 h and fed the basic diet that contained glutamine (0 and 10 g/kg) and glucose (0 and 10 g/kg). Compared with the positive control group, acute heat stress without glutamine and glucose supplementation increased (P < 0.05) drip loss, L* values, and AMPK concentrations, but it decreased (P < 0.05) water-holding capacity, moisture, pH, a* values, b* values, and glutamine concentrations in pectoralis major meat of chickens. However, dietary glutamine (10 g/kg) increased (P < 0.05) water-holding capacity, moisture, pH, a* values, b* values, and glutamine concentrations, while it decreased (P < 0.05) drip loss, L* values, and AMPK concentrations in heat-stressed chicken pectoralis major meat. Dietary glucose (10 g/kg) increased (P < 0.05) water-holding capacity, moisture, pH, and a* and b* values, while it decreased (P < 0.05) L* values and AMPK concentrations of pectoralis major meat in chickens exposed to acute high temperature. There were significant interactions between glutamine and glucose in the water-holding capacity, pH values, AMPK, and glutamine levels of pectoralis major meat in the heat-stressed chickens. The above results suggest that the addition of glutamine and glucose in the diet is necessary for broilers during acute heat stress condition.  相似文献   
4.
玉米果穗发育的生理特性研究   总被引:1,自引:0,他引:1       下载免费PDF全文
为了探讨玉米优良自交系选育中出现短苞叶品种的原因,从生理角度分析了两玉米自交系品种穗轴与苞叶生长发育变化趋势。结果表明:四个时期中139号苞叶硝酸还原酶活性非常低,对照1号的稍高一些。139号苞叶谷氨酰胺合成酶活性小于1号,且1号的酶活性变化较平缓。139号雌穗轴硝酸还原酶活性变化剧烈,授粉后15d达高峰,明显大于1号。139号雌穗轴谷氨酰胺合成酶活性前三时期始终大于1号,最后一时期二者几乎相等,但1号的酶活性变化平缓。就上述结果从氮代谢方面分析了139号苞叶与穗轴发育失调的原因。  相似文献   
5.
【目的】氨酰-tRNA合成酶(aminoacyl-tRNA synthetases, aaRSs)与遗传信息传递密切相关,已发现植物中aaRSs家族蛋白在维持翻译功能之余,还参与配子发生与胚发育、质体的早期发育以及免疫信号的感知与病害防御等生物学过程。本研究利用水稻胚乳发育缺陷突变体,分析水稻色氨酰-tRNA合成酶(WRS1)在胚乳发育中的作用,证明WRS1基因编码一个影响水稻胚乳发育的关键因子。【方法】本研究通过甲烷磺酸乙酯(ethyl methane sulfonate, EMS)诱变籼稻(Oryza sativa subsp. indica)品种N22,筛选到一个稳定遗传的水稻粉质胚乳突变体(wrs1),图位克隆获得目标基因。对wrs1成熟种子进行形态学观察以及淀粉相关理化性质测定,利用细胞学切片分析wrs1发育中胚乳的结构,利用实时荧光定量PCR(quantitative real-time PCR, qRT-PCR)和GUS活性染色分析基因表达模式,通过qRT-PCR比较野生型与突变体花后12 d胚乳中淀粉合成相关基因表达情况,免疫印迹检测野生型与突变体成熟种子中淀粉合成酶蛋白积累情况,使用全自动氨基酸分析仪测定游离氨基酸含量。【结果】 wrs1突变体幼苗表现出明显的发育滞后且逐渐蔫萎死亡,从杂合突变体(WRS1wrs1)中分离到的粉质籽粒呈现明显的腹部皱缩,粒厚、千粒重下降,同时总淀粉含量下降,糊化淀粉的峰值黏度和崩解值均低于野生型。wrs1突变体发育胚乳中复合淀粉颗粒变小,排列疏松。WRS1定位于第12染色体长臂约183 kb的区间内,测序发现编码色氨酰-tRNA合成酶(tryptophanyl-tRNA synthetase, WRS)基因的第6外显子上发生单碱基替换,导致一个保守位置上的甲硫氨酸被替换。wrs1突变体中大部分淀粉合成相关基因表达量下调,且野生型与突变体间基因表达的变化与相应蛋白积累的差异存在不一致的趋势。wrs1突变体籽粒中蛋白质积累降低,而游离氨基酸含量显著升高。【结论】 WRS1编码色氨酰-tRNA合成酶,该基因突变后通过影响氨基酸稳态和蛋白质合成,造成淀粉合成相关基因异常表达从而影响淀粉的合成与积累,导致种子发育缺陷。  相似文献   
6.
【目的】水稻种子主要以淀粉形式储藏能量。淀粉合成需要多种酶类和调控因子参与,机制较为复杂。本研究利用水稻胚乳发育缺陷突变体,克隆和鉴定新的调控淀粉合成相关基因,旨在为研究淀粉合成及其调控提供理论依据。【方法】从化学诱变剂甲基亚硝基脲(1-methyl-1-nitroso-urea, MNU)处理的宁粳3号(Ningjing 3, WT)突变体库中筛选到一个能稳定遗传的胚乳粉质皱缩突变体,命名为fse4 (floury and shrunken 4 )。与籼稻品种Dular杂交获得F1种子(F2),通过图位克隆的策略确定FSE4候选基因。利用杂合植株(FSE4fse4)分离出的粉质种子,观察形态学特征,分析其理化性质。使用扫描电镜和半薄切片技术观察胚乳结构。使用qRT-PCR和免疫印迹分析淀粉合成相关基因表达模式和淀粉合成相关酶类的蛋白积累量。利用全自动氨基酸分析仪测定成熟胚乳各氨基酸含量。【结果】突变体fse4籽粒宽度、厚度以及千粒重显著下降,同时胚乳中总淀粉、总蛋白、直链淀粉含量亦显著下降,而脂肪含量显著上升;淀粉黏度、崩解值和消减值显著低于野生型。突变体fse4中多为单粒型淀粉颗粒,且排列分散。FSE4定位于第5染色体长臂约252 kb的区间内,测序发现编码Δ1-吡咯啉-5-羧酸合成酶基因 (Delta 1-pyrroline-5-carboxylate synthetase, P5CS)第1外显子上发生单碱基替换,导致一保守的氨基酸发生变异。突变体fse4中大部分淀粉合成相关基因表达量下调,多种淀粉合成相关蛋白积累量减少。突变体fse4米粉中多种氨基酸含量发生显著变化,游离氨基酸含量是其野生型的3.6倍。此外,外源喷施脯氨酸能部分恢复突变体fse4种子萌发缺陷表型。【结论】FSE4编码脯氨酸合成关键限速酶P5CS,该基因对胚乳中氨基酸的合成及代谢起重要的调控作用,并影响淀粉的合成与积累。  相似文献   
7.
为探讨C-Myc表达、谷氨酰胺代谢和神经坏死病毒复制三者之间的关系,本研究首先克隆了斜带石斑鱼鳍条细胞(GF-1)中的C-Myc基因(GF-1-C-Myc),结果显示GF-1-CMyc基因cDNA全长814 bp,开放阅读框(ORF)为285 bp,编码95个氨基酸(aa),有亮氨酸拉链结构域与螺旋-环-螺旋(HLH)结构域。实验表达和纯化了GF-1-C-Myc蛋白,并制备其多克隆抗体。采用实时定量PCR技术(qRT-PCR)与免疫印迹法(WB)检测了GF-1-C-Myc基因的表达和神经坏死病毒的复制。结果显示,缺乏谷氨酰胺会同时抑制GF-1-C-Myc基因的表达和神经坏死病毒(NNV)的复制,添加谷氨酰胺可同时促进GF-1-C-Myc的表达和NNV的复制;此外,NNV感染可上调GF-1-C-Myc基因的表达,并显著消耗GF-1细胞培养液中的谷氨酰胺。研究表明,GF-1-C-Myc基因可调控宿主谷氨酰胺代谢,从而有利于神经坏死病毒的复制。本结果为防控NNV的感染提供了参考。  相似文献   
8.
The aim of this work was to study the effect of arbuscular mycorrhizal fungus Glomus mosseae on growth and nitrogen (N) metabolism of durum wheat (Tritcum durum) under various P soil contents. The analyses were extended to macro and micronutrient tissue concentrations, nitrate reductase and glutamine synthetase activities, as well as protein, aminoacids, pyridine dinucleotides and adenine nucleotides. Arbuscular mycorrhiza increased wheat growth in soil in which P availability was low and nitrate was the dominant N form. The root colonization occurred at the highest level in plants grown in limiting soil P and was inversely related to soil P content. The micorrhizal wheat plants contained also the highest concentrations of macro (P, K, Ca, N) and micronutrients (Fe, Zn, Mn) as well as free amino acids, protein, NAD, NADP, AMP, ADP, ATP in roots and leaves. In particular, the micronutrient tissue concentrations (Zn, Mn) supported that mycorrhiza actively modulated their uptake limiting interferences and optimizing growth better than the plant roots, like a very efficient “rootstock”. Control plants grown at the highest soil P did not reach the same concentration as the mycorrhizal plants. Nitrate reductase activities in the roots of mycorrhizal plants were higher than in the control ones, while glutamine synthetase activities were highest in the leaves. Protein and amino acids concentrations, as well as AMP, ADP, ATP, NAD(P), and NAD(P)H were also higher than in the control. Among the free amino acids in the roots, the high levels of glutamine, asparagine, arginine, support the view that ammonium was transferred through the arbuscules to the root cells where it was re‐assimilated in the cortical cells, forming high N : C ratio‐amino acids. They were transferred to the leaves where all the other N compounds could be largely synthesized using the carbon skeletons supplied by photosynthesis.  相似文献   
9.
采用溶液培养试验,研究了氮素不同形态配比对菠菜茎叶中游离氨基酸含量及3种主要氮代谢酶活性的影响。结果表明:1)随着营养液中铵硝比(NH4+-N/NO3--N)的降低,菠菜茎叶中游离氨基酸的总量呈下降趋势。在全硝营养下(NH4+-N/NO3--N=0∶100)下,菠菜茎叶中游离氨基酸的总量只有全铵营养(NH4+-N/NO3--N=100∶0)的34.4%。2)在全铵营养下,菠菜茎叶中游离氨基酸的主要组分是谷氨酰胺、精氨酸和谷氨酸,三者占游离氨基酸总量的百分比依次为39.8%、20.2%和8.9%;在全硝营养下,菠菜茎叶中游离氨基酸以谷氨酸、天冬氨酸和丝氨酸为主,三者占游离氨基酸总量的百分比分别为30.3%1、8.6%和8.5%。3)提高营养液中硝态氮的比例,可以显着提高菠菜茎叶中硝酸还原酶(NR)的活性,同时降低了谷氨酸脱氢酶(GDH)的活性,谷氨酰胺合成酶(GS)活性则呈现先升后降的抛物线状变化规律。4)菠菜茎叶中NR活性与谷胺酰胺含量之间存在着显著负相关关系(r=-0.968)。  相似文献   
10.
保护性耕作是改善农田土壤肥力的重要举措,然而其对作物氮吸收与产量的作用尚不明确。为此,本试验于2016—2017年稻季在湖北省武穴市花桥镇,设置常规翻耕与免耕两种耕作方式以及前茬作物秸秆全量还田与不还田两种秸秆还田方法,研究耕作与秸秆还田方式对稻田土壤N2O排放、根系酶活性、水稻氮吸收与产量的影响。结果表明,耕作方式显著影响土壤N2O排放,但不影响根系硝酸还原酶与谷氨酰胺合成酶活性、水稻氮吸收与产量。与翻耕处理相比,免耕处理2016年和2017年土壤N2O排放量分别显著提高了12.5%~18.2%和21.1%~38.6%。秸秆还田显著影响土壤N2O排放量、根系酶活性、水稻氮吸收与产量。相对于秸秆不还田处理,秸秆还田处理2016年和2017年土壤N2O排放量分别显著提高了38.5%~45.5%和13.1%~29.5%。秸秆还田处理相对于不还田处理根系硝酸还原酶与谷氨酰胺合成酶活性分别显著增加了6.7%~45.9%和9.0%~46.7%,水稻氮吸收量提高了12.5%~26.0%,产量增加了9.4%~12.6%。本文认为,虽然秸秆还田提高了水稻氮吸收与产量,但也促进了土壤N2O的排放,因此在评估保护性耕作稻田温室效应时应加强对温室气体(CH4和N2O)排放和土壤碳固定影响的长期监测,以期为发展低碳稻作提供理论依据和技术支撑。  相似文献   
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