无损测技术在番茄营养诊断中的应用研究

为了实现番茄无损测试诊断的目标,利用叶绿素仪SPAD-502测定了番茄不同生育期成叶、新叶的SPAD读数值。结果表明:番茄无论新叶还是成叶全氮含量、叶绿素含量都与SPAD测定值有很好的相关性;随着施肥量的增加,番茄植株体内的叶绿素含量、全氮含量都在增加,番茄SPAD读数在逐渐的增大,番茄的维生素C含量呈上升趋势,在600kg/hm~2时,果实维生素C含量达到最大值,当施氮量为900kg/hm~2时,番茄体内的可溶性固形物达到了最大值。SPAD能够对番茄的营养状况作出诊断。     

miR-140-3p inhibits viability,invasion and migration of non-small-cell lung cancer A549 cells by targeting PD-L1

AIM: To explore the target relationship between microRNA-140-3p (miR-140-3p) and programmed cell death ligand 1 (PD-L1) and their effect on the viability, migration and invasion of non-small-cell lung cancer A549 cells.METHODS: RT-qPCR was used to detect the miR-140-3p expression in HLF-1, A549 and H1299 cells, and then the A549 cells with the most significant difference were selected as the subsequent research object. TargetScan software and dual-luciferase reporter assay were performed to predict and confirm the target relationship between miR-140-3p and PD-L1. RT-qPCR and Western blot were used to determine the effects of miR-140-3p mimic and inhibitor on PD-L1 expression level. MTT assay was used to detect the viability of A549 cells. Transwell assay was performed to detect the migration and invasion abilities of the A549 cells.RESULTS: miR-140-3p was significantly down-regulated in the A549 cells and H1299 cells (P<0.05). Transfection with miR-140-3p mimic decreased the expression of PD-L1 and inhibited the viability, migration and invasion of the A549 cells. Transfection with pcDNA3.0-PD-L1 reversed the inhibitory effect of miR-140-3p on the viability, migration and invasion of the A549 cells.CONCLUSION: miR-140-3p inhibits the viability, migration and invasion of A549 cells by targeting PD-L1.     

Reversing effect of naringin on cisplatin resistance in human lung cancer A549/DDP cells

AIM: To investigate the effect of naringin (NRG) on cisplatin (DDP) resistance in human lung cancer A549/DDP cells and its possible mechanism. METHODS: A549/DDP cells were cultured in vitro and treated with NRG and/or DDP at different concentrations for 24 h, and then the cell viability were measured by CCK-8 assay. The combination index (CI) of NRG and DDP were analyzed by Chou-Talalay method. The apoptosis rate was analyzed by flow cytometry. Western blot was performed to detect the protein levels of P-glycoprotein (P-gp), multidrug resistance-associated protein 1 (MRP1), p-Akt, CXC chemokine receptor 4 (CXCR4), cleaved caspase-3, Bcl-2 and Bax.RESULTS: The protein levels of P-gp, MRP1, p-Akt and CXCR4 in the A549/DDP cells were higher than those in the A549 cells (P<0.05). The cell viability was remarkably reduced in a dose-dependent manner when A549/DDP cells were exposed to NRG and/or DDP (P<0.05), and the IC₅₀ values of NRG and DDP were 36.92 μmol/L and 129.77 μmol/L, respectively. When the inhibition rate exceeded 15%, NRG in combination with DDP produced a synergistic effect (CI<1). Combination treatment with NRG and DDP significantly induced apoptosis (P<0.05), up-regulated the protein levels of cleaved caspase-3 and Bax, and down-regulated the protein level of Bcl-2 (P<0.05). Meanwhile, NRG remarkably down-regulated the protein levels of P-gp, MRP1, p-Akt and CXCR4 in a dose-dependent manner (P<0.05). CONCLUSION: NRG may enhance the sensibility of A549/DDP cells to DDP most likely via up-regulating the protein level of Bax and down-regulating the protein levels of Bcl-2, P-gp, MRP1, p-Akt and CXCR4.     

Regulatory effect of astragaloside IV on SDF-1α/CXCR4 in EPCs

AIM: To investigate the effects of astragaloside IV (AS-IV) on chemokine receptor 4 (CXCR4) and stromal cell-derived factor 1α (SDF-1α) in endothelial progenitor cells (EPCs) and its mechanism. METHODS: Rat bone marrow-derived EPCs were cultured in vitro. The proliferation, adhesion, migration, apoptosis and tube formation capacity of EPCs treated with AS-IV and AMD3100, a specific blocker of CXCR4, were observed. The effects of AS-IV on the expression of SDF-1α/CXCR4 at mRNA and protein levels and the protein level of p-CXCR4 in the EPCs were determined. RESULTS: AS-IV significantly enhanced the proliferation, adhesion, migration and tube formation abilities of EPCs, reduced the apoptosis of EPCs, and up-regulated the mRNA and protein expression of SDF-1α and CXCR4 and the p-CXCR4 protein level in the EPCs. On the other hand, AMD3100 blocked the up-regulating effect of AS-IV on the mRNA and protein expression of CXCR4 and the p-CXCR4 protein level in the EPCs, but did not affect the effect of AS-IV on the expression of SDF-1α. CONCLUSION: AS-IV might enhance the biological function of EPCs by regulating the expression of SDF-1α/CXCR in EPCs.     

枯草芽孢杆菌在番茄病害防治上的应用与研究进展

综述了枯草芽孢杆菌在防治植物病害中的生防机制,包括竞争作用、拮抗作用、溶菌作用、诱导植物产生抗性和促进植物生长5个方面,介绍了枯草芽孢杆菌在6种番茄病害即灰霉病、青枯病、早疫病、立枯病、枯萎病、根腐病防治中的应用,并对其应用中存在的主要问题进行了总结、前景进行了展望.     

赤霉素对云南省6种常见茄科砧木种子萌发的影响

以水茄、红茄、大苦子、小苦子、刺茄、超级托鲁巴姆6种云南常见茄科砧木种子为材料,采用不同浓度梯度GA3处理种子并统计其动态发芽率和发芽势,进而分析不同浓度GA3对砧木种子萌发的影响.试验结果表明,与对照相比,GA3浓度为200～400 mg/L时,均能提高6种供试砧木种子的发芽率和发芽势;GA3浓度为200～600 m...     

连续施用有机肥对黄瓜体内Zn的积累及其在亚细胞分布的影响

以黄瓜品种'津优35号'为试材,采用田间随机区组试验设计,研究了不同用量(0、15、30、45 t·hm-2和60 t·hm-2)鸡粪源有机肥中Zn在土壤中的积累,以及Zn在黄瓜体内的吸收转运及其在亚细胞各组分中的分布情况,以期为指导黄瓜的安全生产以及鸡粪有机肥合理施用提供参考依据.结果 表明:低用量鸡粪有机肥施用就能显著提高土壤Zn含量(P＜0.05),土壤Zn含量最高为140.40 mg·kg-1,均未超出国家安全标准.施用60 t·hm-2鸡粪有机肥显著提高了黄瓜根部和果实Zn含量,黄瓜果实Zn含量变化范围为19.27～23.59 mg·kg-1,但Zn含量均未超过100 mg·kg-1,可以安全食用.无论鸡粪施用量的高低,Zn在黄瓜根、茎、叶和果实各亚细胞组分中均表现为可溶性组分＜细胞器(叶绿体和线粒体)＜细胞壁.60 t·hm-2鸡粪有机肥可以显著提高黄瓜根部细胞壁Zn含量,且根部细胞壁中Zn含量及所占比例随着鸡粪有机肥施用量的增加而增加.细胞壁中Zn在根中所占比例最高,达到了54.67％～58.77％.     

改良石蜡切片法观察金针菇子实体不同发育时期组织结构

运用改良石蜡切片法制备了金针菇(Flammulina filiformis)子实体不同发育时期的切片,观察其菌褶和菌柄的细胞结构。结果表明,以柠檬烯为透明剂,金针菇子实体组织结构清晰、完整、无皱缩。观察不同发育时期的金针菇子实体组织切片发现,金针菇原基内部有呈菌丝无规则扭结状态的菌盖结构,随着子实体不断发育,菌盖下端有菌褶结构分化,随后菌柄结构随菌盖发育而进一步分化,菌柄组织细胞状纵向紧密排列,横切面有维管束状细胞呈外紧密内疏松状排列且其间有孔洞出现,菌褶菌髓部呈菌丝与球泡状细胞共同存在的异型分布结构。     

西行真菌考察

本文通过对秦岭以西部分地区的一次真菌考察,记述了行程中所见所闻,特别是途径白 龙江原始森林,天险腊子口,茫茫的玛曲若尔盖草原、著名风景区九寨沟、大熊猫自然保护区及古城武都等地考察,发现了丰富的食用,药用等真菌物种资源,同时还提及到历史文化,有益于增加对我国西部的一些了解。     

不同氮磷钾配比对仙客来生长的影响

对仙客来无土栽培营养液中N、P、K元素采用三因素二次D-饱和最优设计,探讨不同浓度氮磷钾对仙客来生长发育的影响,对仙客来的根长、根体积、球茎直径、花朵数、花瓣长、可溶性糖含量、MDA含量、蛋白质含量、叶绿素含量进行分析。结果表明:经方差分析和主成分分析得出,无土栽培仙客来氮、磷、钾最优组合方案为:86.6~263.4、60~100和250~400 mg/L,即氮:磷:钾为3∶1∶6.5。