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旭月NMT简报---关键词搜索:

Int J Mol Sci:福建农林大学丨OsCIPK2过表达促进低氮条件下水稻NO3-​吸收(附NMT实验体系)

转自中关村旭月非损伤微测技术产业联盟


期刊:International Journal of Molecular Sciences
主题:OsCIPK2过表达促进低氮条件下水稻NO3-吸收
标题:Exploring the Potential of Overexpressed OsCIPK2 Rice as a Nitrogen Utilization E cient Crop and Analysis of Its Associated Rhizo-Compartmental Microbial Communities
影响因子:4.183
检测指标:Ca2+、NH4+、NO3-流速
检测样品:水稻根尖
Ca2+、NH4+、NO3-流实验处理方法:幼苗长至三叶期,分别在正常氮(1.44 mM NH4NO3)和低氮(0.24 mM NH4NO3)处理
Ca2+、NH4+、NO3-流实验测试液成份:Ca2+: 0.1 mmol/L KCl, 0.1 mmol/L CaCl2, 0.1 mmol/L MgCl2, 0.5 mol/L NaCl, 0.3 mmol/L MES, 0.2 mmol/L Na2SO4, pH 6.0;
NO3-: 0.1 mmol/L NH4NO3, 0.1 mmol/L NH4NO3, 0.1 mmol/L KCl, 0.1 mmol/L KCl, 0.1 mmol/L KCl2, 0.3 mmol/CaCl2, 0.3 mmol/L MgCl2, 0.3 mmol;
NH4+: 0.1 mmol/L NH4NO3, 0.1 mmol/L CaCl2, 0.3 mmol/L MES, pH 6.0
作者:福建农林大学林文雄

英文摘要

Nitrogen (N) is one of the indispensable factors in rice growth and development. China holds a premier position in the production of rice and at the same time also faces higher N fertilizer costs along with serious damage to the environment. A better solution is much needed to address these issues, without disrupting the production of rice as an important cereal, while minimizing all the deleterious effects on the environment.

Two isogenic lines Kitaake (WT) and its genetically modified line CIPK2 (RC), overexpressing the gene for Calcineurin B-like interacting protein kinase 2 (OsCIPK2) with better nitrogen use efficiency (NUE), were compared for their growth and development under low versus normal levels of N. NUE is a complex trait mainly related to a plant’s efficiency in extraction, assimilation, and recycling of N from soil. The microbial population was analyzed using high-throughput Illumina Miseq 16S rRNA sequencing and found that RC with CIPK2, specifically expressed in rice root, not only performed better without nitrogen fertilizer (LN) but also increased the diversity of bacterial communities in rice rhizosphere compartments (rhizosphere, rhizoplane, and endosphere).

The relative abundance of beneficial bacteria phyla increased, which are known to promote the circulation and transformation of N in rhizosphere soil. To further explore the potential of RC regarding better performance under LN, the ion fluxes in root apical were detected by non-invasive micro-test technique (NMT). We found that RC can absorb more Ca2+ and NO3 under LN as compared to WT. Finally, compared to WT, RC plants exhibited better growth of root and shoot, and increased yield and N uptake under LN, whereas there was no significant difference in the growth of two rice lines under normal nitrogen (NN) treatment.

We are able to get preliminary results, dealing with the OsCIPK2 overexpressed rice line, by studying the rice molecular, physiological, and chemical parameters related to NUE. The results laid the foundation for further research on N absorption and utilization in rice from the soil and the interaction with microbial communities.

 

中文摘要(谷歌机翻译)

氮(N)是水稻生长发育不可或缺的因素之一。中国在大米生产中处于领先地位,同时也面临着更高的氮肥成本以及对环境的严重破坏。迫切需要一种更好的解决方案来解决这些问题,同时又不中断作为重要谷物的大米的生产,同时将对环境的所有有害影响降至最低。

比较了两个同基因系Kitaake(WT)及其基因改造品系CIPK2(RC),它们以较低的氮素利用效率(NUE)过量表达了钙调磷酸酶B样相互作用蛋白激酶2(OsCIPK2)的基因,并在低温下对其生长发育进行了比较。与正常水平的氮相比。NUE是一个复杂的性状,主要与植物从土壤中提取,吸收和循环利用N的效率有关。使用高通量Illumina Miseq 16S rRNA测序分析了微生物种群,发现带有CIPK2的RC在水稻根部特异表达,不仅在不使用氮肥(LN)的情况下表现更好,而且增加了水稻根际区室细菌群落的多样性(根际,根际和内球)。

有益菌门的相对丰度增加,已知它可以促进根际土壤中氮的循环和转化。为了进一步探索RC在LN下获得更好性能的潜力,通过无创微测试技术(NMT)检测了根尖中的离子通量。我们发现,与野生型相比,RC在LN下可以吸收更多的Ca2+和NO3-。最后,与WT相比,RC植物在LN下表现出更好的根和茎生长,并增加了产量和氮素吸收,而在正常氮(NN)处理下,两个水稻品系的生长没有显着差异。

通过研究与NUE相关的水稻分子,生理和化学参数,我们能够获得初步结果,处理过表达OsCIPK2的水稻品系。研究结果为进一步研究水稻从土壤中吸收和利用氮以及与微生物群落的相互作用奠定了基础。

 

结果表明:LN(low nitrogen)处理时,RC(过表达型)根系的Ca2+吸收显著增加,而NN(normal nitrogen)处理时无显著差异;LN处理时,RC根系的NO3-吸收增加,而NN条件下RC和WT(野生型)根系的NO3-表现为外排,且二者并无显著差异;至于NH4+,RC和WT均表现为外排,且无显著差异。这说明,LN条件下,根系CIPK2基因过表达促进了根系吸收NO3-,与RC根际的硝化作用增加是符合的。

文章链接:https://www.mdpi.com/1422-0067/20/15/3636

 

 

SCI REP-UK :山东农大丨NaCl胁迫下磁处理可调控杨树N代谢(附NMT实验体系)

转自中关村旭月非损伤微测技术产业联盟


期刊:Scientific Report
主题:NaCl胁迫下磁处理可调控杨树N代谢
标题:The effects of magnetic treatment on nitrogen absorption and distribution in seedlings of Populus × euramericana ‘Neva’ under NaCl stress
影响因子:4.011
检测指标:NH4+、NO3-流速
检测样品:杨树根伸长区(距根尖15mm)和叶肉细胞
NH4+、NO3-流实验处理方法:4周龄杨树幼苗,分别经0g/L NaCl+磁化(M0),0g/L NaCl+非磁化(NM0),4g/L NaCl+磁化(M4),4g/L NaCl+非磁化(NM4)处理
NH4+、NO3-流实验测试液成份:NH4+: 0.1 mM NH4NO3, 0.1 mM CaCl2, 0.3 mM MES, pH 5.5
NO3-: 0.1 mM NH4NO3, 1.0 mM KCl, 0.1 mM CaCl2, 0.3 mM MES, pH 5.5
作者:山东农业大学林学院马风云、刘秀梅

英文摘要

A potted experiment with Populus × euramericana ‘Neva’ was carried out to assess whether there are positive effects of magnetic treatment of saline water (MTSW) on nitrogen metabolism under controlled conditions in a greenhouse. Growth properties, nitrogen contents, enzyme activities and metabolite concentrations were determined based on field experiments and laboratory analysis after a 30-day treatment.

The results were as follows: (1) Biomass accumulation, root morphological properties and total nitrogen content were improved by MTSW. (2) Magnetization led to a greater increase in nitrate-nitrogen (NO3-N) content in roots than in leaves, accompanied by greater NO3 efflux and activated nitrate reductase. (3) MTSW led to a higher ammonium-nitrogen (NH4+-N) content and greater uptake of net NH4+ in the leaves than that in the roots. (4) Magnetization stimulated glutamine synthase, glutamate dehydrogenase and glutamate synthase activities, whereas the concentrations of glutathione and oxidized glutathione were increased in leaves but decreased in roots, and the total glutathione content was increased.

Overall, these results indicated some beneficial impacts of MTSW on nitrogen translocation under field conditions, especially for equilibrating the distribution of NO3-N and NH4+-N. Moreover, these findings confirmed the potential of using low-quality water for agriculture.

 

中文摘要(谷歌机翻译)

进行了盆栽的“ Neva”杨树的盆栽实验,以评估在受控条件下温室中磁化盐水(MTSW)对氮素代谢是否有积极作用。经过30天的处理后,根据田间实验和实验室分析确定了生长特性,氮含量,酶活性和代谢物浓度。

结果表明:(1)MTSW提高了生物量积累,根系形态特征和总氮含量。(2)磁化作用导致根部的硝酸盐氮(NO3-N)含量比叶片中的增加更大,同时伴随着更大的NO3-流出量和活化的硝酸还原酶。(3)MTSW导致叶片中的铵态氮(NH4+ -N)含量更高,并且比根部更高地吸收了净NH4+。(4)磁化刺激谷氨酰胺合酶,谷氨酸脱氢酶和谷氨酸合酶活性,而叶片中谷胱甘肽和氧化型谷胱甘肽的浓度增加,而根部减少,谷胱甘肽总含量增加。

总体而言,这些结果表明,MTSW对田间条件下的氮转运有一些有益的影响,尤其是对于平衡NO3- -N和NH4+ -N的分布。此外,这些发现证实了将低质水用于农业的潜力。

 

结果表明:对于NO3-,叶肉细胞和根伸长区均表现为外排。存在NaCl胁迫时,磁疗前后,叶肉细胞的NO3-外排速率从235.09 pmol·cm-2·s-1(NM4)增加到290.23 pmol·cm-2·s-1(M4);经NaCl胁迫后,根伸长区的NO3-外排速率从123.53 pmol·cm-2·s-1(M4)增加到157.51 pmol·cm-2·s-1(NM4)。
至于NH4+,叶肉细胞表现为吸收而根伸长区表现为外排。经NaCl胁迫后,叶肉细胞的NH4+吸收速率降低,NM0和NM4并无显著差异。但在根伸长区,NaCl胁迫后NH4+外排速率更高,M4的外排速率达到了186.83 pmol·cm-2·s-1

文章链接:https://www.nature.com/articles/s41598-019-45719-6

 

Bone :山西医科大第二医院丨DAla2GIP抑制钙吸收拮抗软骨细胞凋亡(附NMT实验体系)

转自中关村旭月非损伤微测技术产业联盟


期刊:Bone
主题:DAla2GIP抑制钙吸收拮抗软骨细胞凋亡
标题:DAla2GIP antagonizes H2O2-induced chondrocyte apoptosis and inflammatory factor secretion
影响因子:4.360
检测指标:Ca2+流速
检测样品:7日龄小鼠,1.0ml乙醚麻醉后处死,第三代胸部软骨组织细胞
Ca2+流实验处理方法:Control,300μM H2O2 ,100pM DAla2GIP 和 300μM H2O2 + 100pM DAla2GIP
Ca2+流实验测试液成份:
作者:山西医科大学第二医院卫小春、王宇泽

英文摘要

To investigate the protective effects of DAla2GIP against the apoptosis and inflammatory factor secretion in H2O2-induced chondrocyte, and explore the possible mechanisms of DAla2GIP underlying its protection.

The chondrocytes were divided into the following four groups: Control, 300 μM H2O2, 100 pM DAla2GIP and 300 μM H2O2 + 100 pM DAla2GIP. The apoptosis of chondrocyte was measured by using mitochondrial membrane potential assay kit (JC-1) and TUNEL assay, the inflammatory factor secretion were assessed by ELISA assay, and the cellular and molecular mechanisms of DAla2GIP protection were investigated by using Real time-PCR, flow cytometry, Non- invasive calcium detection and western blotting techniques.

(1) DAPla2GIP prevents apoptosis of chondrocyte induced by H2O2. (2) DAla2GIP alleviated the inflammation of chondrocyte induced by H2O2. (3) DAla2GIP prevents chondrocyte apoptosis by inhibiting calcium influx of chondrocyte and regulating expression of Bcl-2 and Caspase-3induced by H2O2. (4) DAla2GIP inhibited the H2O2 mediated inflammation by up- regulating the expressions of Sox9 and Col2a1 and inhibiting PI3K/Akt/NF-κB pathway.

Our experimental results revealed that DAla2GIP prevents chondrocyte apoptosis by inhibiting calcium influx of chondrocyte and induced regulating expression of Bcl-2 and Casp ase-3by H2O2. Further, molecular biology experiments confirmed that DAla2GIP inhibited the H2O2 mediated inflammation vis up-regulating the expressions of Sox9 and Col2a1 and inhibiting PI3K/Akt/NF-κB pathway. The results demonstrate that DAla2GIP has protective properties in H2O2-induced chondrocyte injury, this finding shows that novel GIP analogues have the potential as a novel therapeutic for osteoarthritis patients.

 

中文摘要(谷歌机翻译)

研究DAla2GIP对H2O2诱导的软骨细胞凋亡和炎性因子分泌的保护作用,并探讨DAla2GIP保护其的可能机制。

软骨细胞分为以下四组:对照组,300μmH2O2、100μmM DAla2GIP和300μmH2O2n +100μpMDAla2GIP。用线粒体膜电位分析试剂盒(JC-1)和TUNEL法检测软骨细胞的凋亡,用ELISA法评估炎性因子的分泌,并通过实时PCR研究DAla2GIP保护的细胞和分子机制,流式细胞仪,无创钙离子检测和蛋白质印迹技术。

(1)DAPla2GIP可防止H2O2诱导的软骨细胞凋亡。(2)DAla2GIP减轻了H2O2诱导的软骨细胞炎症。 (3)DAla2GIP通过抑制软骨细胞的钙内流并调节过氧化氢诱导的Bcl-2和Caspase-3的表达来防止软骨细胞凋亡。(4)DAla2GIP通过上调Sox9和Col2a1的表达并抑制PI3K / Akt /NF-κB通路来抑制H2O2介导的炎症。

我们的实验结果表明,DAla2GIP通过抑制软骨细胞的钙内流并诱导H2O2调节Bcl-2和Casp ase-3的表达来防止软骨细胞凋亡。此外,分子生物学实验证实,DAla2GIP通过上调Sox9和Col2a1的表达并抑制PI3K / Akt /NF-κB通路来抑制H2O2介导的炎症。结果表明,DAla2GIP在H2O2诱导的软骨细胞损伤中具有保护性,这一发现表明,新型GIP类似物具有作为骨关节炎患者的新型治疗剂的潜力。

 

结果表明:100 pM DAla2-GIP组和Control组的Ca2+吸收速率并无显著差异,平均值分别是1.94 pmol·cm-2·s-1和1.42 pmol·cm-2·s-1;经300 μM H2O2处理后,Ca2+吸收速率明显增加,平均值为139.61 pmol·cm-2·s-1;经300 μM H2O2和100 pM DAla2-GIP共同处理后,Ca2+吸收速率明显低于300 μM H2O2处理组,平均值为26.68 pmol·cm-2·s-1,说明DAla2-GIP抑制了H2O2诱导的Ca2+吸收。而Ca2+吸收是软骨细胞凋亡早期的标志。

文章链接:https://www.sciencedirect.com/science/article/abs/pii/S8756328219302091?via%3Dihub

 

 

Genes :北京林业大学丨盐胁迫下钾转运体LrKUP8抑制K+外排(附NMT实验体系)

转自中关村旭月非损伤微测技术产业联盟


期刊:Genes
主题:盐胁迫下钾转运体LrKUP8抑制K+外排
标题:Potassium Transporter LrKUP8 Is Essential for K+ Preservation in Lycium ruthenicum, A Salt-Resistant Desert Shrub
影响因子:3.331
检测指标:K+流速
检测样品:黒枸杞愈伤组织
K+流实验处理方法:有/无300 mM NaCl培养12h
K+流实验测试液成份:0.5 mM KCl, 0.5 mM NaCl, 0.1mM MgCl2, 0.2 mM CaCl2, 2.5% sucrose,pH 5.7
作者:北京林业大学陈金焕、戴逢斌

英文摘要

Salt stress is a major constraint for many crops and trees. A wild species of Goji named Lycium ruthenicum is an important economic halophyte in China and has an extremely high tolerance to salinity. L. ruthenicum grows in saline soil and is known as a potash-rich species.

However, its salt adaptation strategies and ion balance mechanism remains poorly understood. Potassium (K+) is one of the essential macronutrients for plant growth and development. In this study, a putative salt stress-responsive gene encoding a HAK (high-affinity K+)/KUP (K+ uptake)/KT (K+ transporter) transporter was cloned and designated as LrKUP8.

This gene belongs to the cluster II group of the KT/HAK/KUP family. The expression of LrKUP8 was strongly induced under high NaCl concentrations. The OE-LrKUP8 calli grew significantly better than the vector control calli under salt stress conditions. Further estimation by ion content and micro-electrode ion flux indicated a relative weaker K+ efflux in the OE-LrKUP8 calli than in the control.

Thus, a key gene involved in K+ uptake under salt condition was functionally characterized using a newly established L. ruthenicum callus transformation system. The importance of K+ regulation in L. ruthenicum under salt tolerance was highlighted.

 

中文摘要(谷歌机翻译)

盐胁迫是许多农作物和树木的主要限制因素。枸杞的一种野生种,称为枸杞,是中国重要的经济盐生植物,对盐分的耐受性极高。ruthenicum生长在盐渍土壤中,被称为富含钾肥的物种。

然而,其盐适应策略和离子平衡机制仍然知之甚少。钾(K+)是植物生长和发育必不可少的大量营养素之一。在这项研究中,克隆了编码HAK(高亲和力K+)/ KUP(K+摄取)/ KT(K+转运蛋白)转运蛋白的假定盐胁迫响应基因,并将其命名为LrKUP8。

该基因属于KT / HAK / KUP家族的II类。在高NaCl浓度下强烈诱导LrKUP8的表达。在盐胁迫条件下,OE-LrKUP8愈伤组织的生长明显好于载体对照的愈伤组织。通过离子含量和微电极离子通量的进一步估计表明,与对照相比,OE-LrKUP8愈伤组织中的K+外排相对较弱。

因此,使用新建立的黑麦草愈伤组织转化系统对在盐条件下参与钾离子吸收的关键基因进行了功能鉴定。强调了在耐盐性条件下钌中的K+调节的重要性。

 

结果表明:LrKUP8抑制了愈伤组织中K+外排。不存在NaCl胁迫时,两种愈伤组织的K+外排速率较小,且无显著差异。经盐胁迫后,K+外排速率远高于无胁迫组;对照组(pBI121)的K+外排速率明显高于过表达组(OE-LrKUP8)。过表达组由于其更强的保K+能力,因而维持高的K+/Na+比。保持最优的K+/Na+比是植物耐盐性的关键特征之一,证明LrKUP8的保K+能力促进了黒枸杞在盐胁迫下的生长发育。

文章链接:https://www.mdpi.com/2073-4425/10/8/600

 

 

PBJ IAA流新成果:农科院棉花所、浙江农科院丨AKR2A协调IAA和H2O2积累调控棉纤维伸长

转自中关村旭月非损伤微测技术产业联盟


期刊:Plant Biotechnology Journal
主题:AKR2A协调IAA和H2O2积累调控棉纤维伸长
标题:AKR2A participates in the regulation of cotton fibre development by modulating biosynthesis of verylong- chain fatty acids
影响因子:6.840
检测指标:IAA、H2O2流速
检测样品:棉纤维尖端
IAA、H2O2流实验处理方法:15 DPA
IAA、H2O2流实验测试液成份:0.1 mM KCl, 0.1 mM CaCl2, 0.1 mM MgCl2, 0.5 mM NaCl,0.3 mM MES, 0.2 mM Na2SO4 and 0.1% sucrose, pH 6.0
作者:中国农科院棉花所李付广、浙江省农科院沈国新

英文摘要

The biosynthesis of very‐long‐chain fatty acids (VLCFAs) and their transport are required for fibre development. However, whether other regulatory factors are involved in this process is unknown. We report here that overexpression of an Arabidopsis gene ankyrin repeat‐containing protein 2A (AKR2A) in cotton promotes fibre elongation.

RNA‐Seq analysis was employed to elucidate the mechanisms of AKR2A in regulating cotton fibre development. The VLCFA content and the ratio of VLCFAs to short‐chain fatty acids increased in AKR2A transgenic lines. In addition, AKR2A promotes fibre elongation by regulating ethylene and synergizing with the accumulation of auxin and hydrogen peroxide. Analysis of RNA‐Seq data indicates that AKR2A up‐regulates transcript levels of genes involved in VLCFAs’ biosynthesis, ethylene biosynthesis, auxin and hydrogen peroxide signalling, cell wall and cytoskeletal organization. Furthermore, AKR2A interacted with KCS1 in Arabidopsis both in vitro and in vivo. Moreover, the VLCFA content and the ratio of VLCFAs to short‐chain fatty acids increased significantly in seeds of AKR2A‐overexpressing lines and AKR2A/KCS1 co‐overexpressing lines, while AKR2A mutants are the opposite trend.

Our results uncover a novel cotton fibre growth mechanism by which the critical regulator AKR2A promotes fibre development via activating hormone signalling cascade by mediating VLCFA biosynthesis. This study provides a potential candidate gene for improving fibre yield and quality through genetic engineering.

 

中文摘要(谷歌机翻译)

超长链脂肪酸(VLCFA)的生物合成及其运输是纤维发展所必需的。但是,此过程是否涉及其他监管因素尚不清楚。我们在此报告,棉花中拟南芥基因锚蛋白重复序列蛋白2A(AKR2A)的过表达促进了纤维的伸长。

RNA‐Seq分析用于阐明AKR2A调节棉纤维发育的机制。在AKR2A转基因品系中,VLCFA含量和VLCFA与短链脂肪酸的比率增加。另外,AKR2A通过调节乙烯并与植物生长素和过氧化氢的积累协同作用来促进纤维伸长。RNA-Seq数据分析表明,AKR2A上调参与VLCFAs生物合成,乙烯生物合成,生长素和过氧化氢信号,细胞壁和细胞骨架组织的基因的转录水平。此外,在体外和体内,AKR2A与拟南芥中的KCS1相互作用。此外,AKR2A过表达品系和AKR2A / KCS1共过表达品系的种子中VLCFA含量和VLCFA与短链脂肪酸的比率显着增加,而AKR2A突变体则相反。

我们的结果揭示了一种新颖的棉纤维生长机制,关键调节剂AKR2A通过介导VLCFA生物合成,通过激活激素信号传导级联来促进纤维发育。这项研究为通过基因工程提高纤维产量和质量提供了潜在的候选基因。

 

结果表明:WT中IAA的平均外排速率为4262.30 fmol·cm-2·s-1;而AKR2A-2和AKR2A-57的外排速率平均值分别是14298.01 fmol·cm-2·s-1和13685.83 fmol·cm-2·s-1,显然AKR2A-OE的IAA外排速率明显高于WT。
WT中H2O2的平均外排速率为0.02 pmol·cm-2·s-1;而AKR2A-2和AKR2A-57的吸收速率平均值分别是0.49 pmol·cm-2·s-1和0.80 pmol·cm-2·s-1
相比于WT,AKR2A-OE的IAA外排速率和H2O2吸收速率在纤维伸长过程中明显增加。

文章链接:https://onlinelibrary.wiley.com/doi/full/10.1111/pbi.13221