磷饥饿时番茄幼苗根系质膜H+-ATP酶活性

磷饥饿提高了番茄幼苗质膜H+-ATP酶活性并促进了番茄幼苗根部的H+分泌。动力学分析表明,磷饥饿使番茄幼苗根部质膜H+-ATP酶的Km值明显降低,亦即提高了该酶对其底物的亲和力,但对该酶的Vmax影响不大。另外,磷饥饿并不改变ATP酶的最适pH值(最适pH值为6.5)。钒酸盐显著抑制番茄幼苗根部质膜ATP酶的活性以及H+分泌,也显著抑制番茄幼苗的Pi吸收。与对照相比,上述抑制作用在饥饿处理的植物中表现得更强。以上结果表明,磷饥饿时高亲和性Pi传递系统的诱导很可能包含质膜H+-ATP酶的参与。     

TheRelati磷饥饿时番茄幼苗根系质膜H~ - ATP酶活性的变化与磷吸收的关系(英文)

磷饥饿提高了番茄幼苗质膜H ATP酶活性并促进了番茄幼苗根部的H 分泌。动力学分析表明 ,磷饥饿使番茄幼苗根部质膜H ATP酶的Km 值明显降低 ,亦即提高了该酶对其底物的亲和力 ,但对该酶的Vmax影响不大。另外 ,磷饥饿并不改变ATP酶的最适 pH值 (最适 pH值为 6.5)。钒酸盐显著抑制番茄幼苗根部质膜ATP酶的活性以及H 分泌 ,也显著抑制番茄幼苗的Pi吸收。与对照相比 ,上述抑制作用在饥饿处理的植物中表现得更强。以上结果表明 ,磷饥饿时高亲和性Pi传递系统的诱导很可能包含质膜H ATP酶的参与。     

磷饥饿对番茄幼苗H^＋分泌及Pi吸收的影响

磷饥饿条件下番茄幼苗的Ｈ＾＋分泌速率明显提高,质膜质子泵专一性抑制剂钒酸盐能显著抑制番茄幼苗的Ｈ＾＋分泌,也能显著抑制其Ｐｉ吸收。此结果表明,磷饥饿时番茄幼苗Ｐｉ吸收速率的变化与Ｈ＾＋分泌速率的变化之间可能具有一定的相关性,并进一步暗示质膜Ｈ＾＋－ＡＴＰａｓｅ可能参与其中,本文结果还表明,Ｐｉ／Ｈ＾＋的准量关系约为１：１。     

磷饥饿时番茄幼苗根系质膜H^＋—ATP酶活性的变化与磷吸收的关系

磷饥饿提高了番茄幼苗质膜H^ -ATP酶活性并促进了番茄幼苗根部的H^＋分泌和。动力学分析表明,磷饥饿使番茄功苗根部质膜H^ -ATP酶的K m值明显降低,亦即提高了该酶对其底物的亲和力,但对该酶的Vmax影响不大。另外,磷饥饿并不改变ATP酶的最适pH值（最适pH值为6.5）。钡酸盐显著抑制番茄幼苗根部质膜ATP酶的活性以及H^＋分泌,也显著抑制番茄幼苗的Pi吸收。与对照相比,上述抑制作用在饥饿处理的植物中表现得更强,以上结果表明,磷饥饿时高亲和性Pi传递系统的诱导很可能包含质膜H^ -ATP酶的参与。     

外源γ-氨基丁酸调控甜瓜叶绿体活性氧代谢应对短期盐碱胁迫

以甜瓜品种‘金辉1号’为试材,采用深液流水培法,研究外源γ 氨基丁酸(GABA)对短期盐碱胁迫下甜瓜幼苗叶绿体活性氧代谢的调控作用.结果表明: 盐碱胁迫显著提高了甜瓜叶绿体内光合色素、丙二醛(MDA)和过氧化氢(H₂O₂)含量及超氧阴离子(O^-_·2)产生速率;增加抗坏血酸(AsA)和谷胱甘肽(GSH)等抗氧化物质含量;明显抑制H⁺-ATP酶(H⁺-ATPase)和H⁺ 焦磷酸酶(H⁺-PPiase)活性.外源叶面喷施GABA有效抑制了盐碱胁迫引起的叶绿体内O^-_·2、H₂O₂和MDA的积累,缓解了光合色素增加的趋势;显著提高SOD和AsA GSH循环各个酶的活性,增加了AsA和GSH库,降低了AsA/DHA和GSH/GSSH比值,增强了H⁺-ATPase和H⁺-PPiase 活性.表明外源GABA能加快叶绿体内活性氧代谢,促进AsA-GSH循环的运转,维持细胞膜的渗透性,进而缓解了盐碱胁迫引起的氧化伤害.     

磷酸饥饿时番茄幼苗酸性磷酸酶活性的变化与Pi吸收的关系

磷酸饥饿时,番茄幼苗根部及地上部酸性磷酸酶活性均显著增强,根部细胞表面酸性磷酸酶及根部外泌的酸性磷酸酶活性亦明显提高。动力学分析表明,磷酸饥饿提高了番茄幼苗根部的酸性磷酸酶对其底物的亲和力。另外,磷酸饥饿对番茄幼苗根部酸性磷酸酶活性的最适ｐＨ值没有影响。钼酸对番茄幼苗根部酸性磷酸酶活性有强烈的抑制作用,对番茄幼苗Ｐｉ吸收速率也有十分明显的抑制效果。以上结果表明,磷酸饥饿时,番茄幼苗Ｐｉ吸收的适应性变化可能与根部酸性磷酸酶特别是根部细胞表面酸性磷酸酶及其外泌酸性磷酸酶的参与密切关联。     

盐碱胁迫下碱地肤Na+/H+逆向转运蛋白基因KsNHX1表达分析

利用RACE技术得到碱地肤KsNHX1的3’cDNA序列.分子系统进化分析显示,KsNHX1为液泡膜Na⁺/H⁺逆向转运蛋白编码基因.通过半定量RT-PCR检测了该基因在盐碱胁迫下的表达,结果表明: 200 mmol·L^-1 NaCl胁迫2~24 h,KsNHX1在叶片中表达量持续增加;200 mmol·L^-1 NaCl处理10 h,KsNHX1在根、茎、叶和花中的表达都上调;不同浓度NaCl处理下,叶片中KsNHX1表达上调,160 mmol·L^-1时达到最高;低于400 mmol·L^-1浓度下,根中该基因的表达也都上调.经不同浓度Na₂CO₃胁迫,根中KsNHX1的表达变化趋势与相应浓度NaCl胁迫下的变化相同;但叶片中除160 mmol·L^-1 Na₂CO₃处理下KsNHX1表达略有上调外,其他浓度下KsNHX1的表达都低于对照.KsNHX1的表达模式暗示,在不同盐碱胁迫下,碱地肤能够维持体内相对稳定的K⁺/Na⁺,其耐盐特性可能与Na⁺/H⁺逆向转运蛋白的作用密切相关.     

转AtNHX1基因杨树Tr品系的耐盐性研究

以不同盐分强度处理欧美107杨(Populus × euramericana ‘Neva’) (Wt)和转拟南芥液泡膜Na⁺/H⁺逆向转运蛋白基因AtNHX1欧美107杨新品系(Tr)幼苗, 揭示Tr和Wt两品系幼苗耐盐性的差异, 探索拟南芥液泡膜Na⁺/H⁺逆向转运蛋白基因AtNHX1对提高杨树耐盐能力的效应。结果表明: 低盐处理下, Wt植株生长明显受到抑制, 其干重显著低于对照, 盐分强度加大后, 抑制作用更大, 其干重只有对照的50%; 而Tr植株在低盐处理下干重与对照差异不显著, 高盐处理时其干重为对照的74%。同时, 不同盐度处理下, Tr的干重均显著高于Wt, 且随着盐度升高, 两品系间植株干重差异增大。盐处理后, Tr植株叶片叶绿素和类胡萝卜素的含量均显著高于Wt, 并能维持较高的净光合速率(P_n)和PSII最大光化学效率(F_v/F_m); 在盐处理下虽然Tr叶片和根系均较Wt积累了更多的Na⁺, 但同时也维持了更高的K⁺和K⁺/Na⁺比率, 而且叶片对K⁺选择性的运输明显高于Wt; 同时, Tr叶片MDA含量和电解质渗漏率显著低于Wt。可见, 在盐处理下转AtNHX1植株较未转基因植株维持了更高的生长量、光合色素、光合能力和叶片质膜稳定性, 说明AtNHX1的转入能够显著提高欧美107杨的耐盐性。     

菌株C8和B4的分离鉴定及其耐盐促生效果和机制

土壤盐渍化是影响农业生产的主要环境因素，合理使用根际促生菌是改良修复盐渍化土壤的有效途径。本研究从东营地区盐渍化土壤中分离筛选到两株耐盐促生菌株C8和B4，经形态学特征、生理生化特性、16S rDNA和gyrB基因序列分析，分别鉴定为氧化微杆菌(Microbacterium oxydans)和嗜麦芽窄食单胞菌(Stenotrophomonas maltophilia)。含盐LB培养基上检测结果显示，菌株C8耐6%NaCl，具有解钾、溶有机磷、溶无机磷和分泌生长素的功能；菌株B4耐8%NaCl，具有溶有机磷和分泌生长素的功能。C8和B4单独施用及配施对盐胁迫下番茄的促生作用及机制的试验结果表明，C8和B4单独施用及配施均显著促进盐胁迫下番茄种子萌发和幼苗生长，提高过氧化氢酶(CAT)和过氧化物酶(POD)活性，上调过氧化氢酶基因CAT1和CAT2表达量，增加植株K⁺含量，降低Na⁺含量和Na⁺/K⁺，上调液泡膜Na⁺/H⁺逆向转运蛋白基因NHX1和NHX3的...     

NaHCO3胁迫下3种灌木Na+、K+、Ca2+的吸收及转运

通过盆栽试验,采用原子吸收分光光度法和非损伤微测技术,研究了NaHCO₃胁迫(300 mmol·L^-1)对大洋洲滨藜、四翅滨藜和宁夏枸杞3种灌木离子吸收及运转的影响.结果表明: 随着NaHCO₃浓度升高,两种滨藜和宁夏枸杞叶片中Na⁺含量升高,300 mmol·L^-1NaHCO₃胁迫下,宁夏枸杞叶肉细胞Na⁺的外排增加,两种滨藜净Na⁺外排降低;随着胁迫时间的延长,大洋洲滨藜和宁夏枸杞叶片的K⁺含量下降,Na⁺/K⁺升高,四翅滨藜叶片K⁺含量升高,Na⁺/K⁺降低;随着浓度的升高,宁夏枸杞叶片积累Ca²⁺减少,Na⁺/Ca²⁺高于对照,叶肉细胞Ca²⁺外排;两种滨藜叶Ca²⁺含量总体呈升高趋势,叶肉细胞Ca²⁺表现为内流.在NaHCO₃胁迫下,3种灌木通过不同的策略来消除Na⁺毒害.宁夏枸杞叶片Na⁺的积累抑制了对Ca²⁺的吸收;两种滨藜Ca²⁺的内流促使细胞质中游离Ca²⁺增加,增加的细胞质\[Ca²⁺\]cyt防治质膜H⁺ ATPase去极化,限制K⁺的外排,从而维持细胞内Na⁺/K⁺的平衡,其中四翅滨藜调控Na⁺/K⁺平衡的能力较强.     

Testing the polar auxin transport model with a selective plasma membrane H+-ATPase inhibitor

Auxin is unique among plant hormones in that its function requires polarized transport across plant cells. A chemiosmotic model was proposed to explain how polar auxin transport is derived by the H⁺ gradient across the plasma membrane (PM) established by PM H⁺-adenosine triphosphatases (ATPases). However, a classical genetic approach by mutations in PM H⁺-ATPase members did not result in the ablation of polar auxin distribution, possibly due to functional redundancy in this gene family. To confirm the crucial role of PM H⁺-ATPases in the polar auxin transport model, we employed a chemical genetic approach. Through a chemical screen, we identified protonstatin-1 (PS-1), a selective small-molecule inhibitor of PM H⁺-ATPase activity that inhibits auxin transport. Assays with transgenic plants and yeast strains showed that the activity of PM H⁺-ATPases affects auxin uptake as well as acropetal and basipetal polar auxin transport. We propose that PS-1 can be used as a tool to interrogate the function of PM H⁺-ATPases. Our results support the chemiosmotic model in which PM H⁺-ATPase itself plays a fundamental role in polar auxin transport.     

Relationship between the Changes of Acid Phosphatase Activities and Pi -uptake of Tomato Seedlings during Phosphate Starvation

The acid phosphatase activities from roots and both stems and leaves of tomato seedlings all in-creased markedly under phosphate starvation. Phosphate starvation also increased the activities of acid phos-phatase from cell surface of, and released by roots of tomato seedlings. The kinetic analysis of acid phos-phatase of roots of tomato seedlings revealed that phosphate starvation increased the affinity of the enzyme to its substrate. The results also revealed that phosphate starvation had no effect on the optimum pH (pH 4.93) of the acid phosphatase of roots of tomato seedlings. It was also found that molybdate strongly inhibited not only the activities of acid phosphatase but also Pi- uptake rates of tomato seedlings.     

一氧化氮调节盐胁迫下小麦幼苗根部质膜H+-ATPase和焦磷酸酶活性提高耐盐性

采用外源一氧化氮(NO)供体硝普钠(SNP)研究了NO对盐胁迫下小麦(Triticum aestivum L.)幼苗耐盐性的影响.结果表明,0.1 mmol/L SNP处理显著缓解了1 50 mmol/L NaCl胁迫对小麦幼苗生长的抑制效应,包括水分丧失以及叶绿素降解,从而提高了小麦幼苗的耐盐性.进一步结合1 mg/mL血红蛋白处理则显著逆转了SNP诱导的上述效应;利用亚硝酸钠和铁氰化钾作为对照也证实了NO对小麦幼苗耐盐性的专一性调节作用,并可能与NO对小麦幼苗根部质膜H -ATPase和焦磷酸酶活性诱导有关.此外,尽管NO显著提高了盐胁迫下小麦幼苗根部细胞质膜H -ATPase和焦磷酸酶的ATP水解活性,但是对跨膜H 转运则没有明显影响.应用外源CaSO4和EGTA处理也证实,Ca2 可能在NO诱导的质膜H -ATPase和焦磷酸酶活性的提高过程中起信号作用.另外,分析盐胁迫下小麦幼苗根部Na 和K 含量的变化也发现,NO对Na 含量没有明显影响,但是却显著提高了K 水平和K /Na 比,这可能也是NO提高小麦幼苗耐盐性的原因之一.     

不同生境两种生态型芦苇叶片质膜H+-ATPase的比较

利用两相法化纯化质膜微囊,研究了分布西北沙地区的两种生态型芦苇(Phragmites communis trih.)水生芦苇和重度盐化草甸芦苇,分别简称为水芒和盐芦)叶片质膜H - ATPase的部分性质.结果显示,与水芦相比,盐芦质膜H -ATPase的ATP水解活性升高,Km值由1.27mmol\l降至Vmax没有显著差异.并且该酶活性对温度的敏感必玫PH谱型也发生了变化.以对硝基苯磷酸盐为底物,低浓度时盐芦的的质膜H -ATPase水解活性有差异.钡酸盐抑制实验表明,两种生态的质膜H -ATPase磷酸-酶区的催化性质不同.胰酶对质膜H -ATPase活性的活化谱型也存在差异,说明该酶C末端的结构或性质发生了变化.此外,与水芦相比,盐芦质膜H -ATPase的质子泵活性的耦联程度也升高了.以上结果明,当芦苇从水生环境向盐渍环境过渡时,质膜H -ATPase的催化性质发生了变化,这些变化可能是由酶结构的修饰和不同的同工酬酶谱引起的.H -ATPase催化性质的变化可能是对盐渍生境的适应性反应.     

Influence of ATPase activity on PPi dependent H-transport in tonoplast vesicles of Acer pseudoplatanus

Tonoplast H⁺-ATPase and H⁺-pyrophosphatase (H⁺-PPase) were previously characterized in Acer pseudoplatanus cells (A. Pugin et al., Plant Sci., 73 (1991) 23–34; A. Fraichard et al., Plant Physiol. Biochem., 31 (1993) 349–359). The present study concerns the relationships between these two enzymes in vitro. ATP and PPi hydrolysis were additive and the inhibition of one did not affect the activity of the second one. ATP and PPi H⁺-transports were also additive. The H⁺ -PPase inhibition did not change ATP-dependent H⁺-transport but H⁺-ATPase inhibition inhibited the PPi dependent H⁺-transport. Because H⁺-PPase was reported to transport H⁺ and K⁺ into the vacuole (Davies et al., Proc. Natl. Acad. Sci. USA, 89 (1992) 11701–11705), these results led us to suggest that the inhibition of the H⁺-ATPase activity could modify the H⁺/K⁺ stoichiometry for the benefit of K⁺-transport.     

Phosphorylation-dephosphorylation of membrane proteins controls the microsomal H-ATPase activity of corn roots

The Mg²⁺-dependent H⁺-ATPase activity of a sealed microsomal vesicle fraction isolated from corn (Zea mays L.) roots appears to be controlled by a phosphorylation-dephosphorylation cycle. Phosphorylation of the microsomal fraction is carried out by a Ca²⁺/calmodulin (CaM)-stimulated process. The H⁺-ATPase activity decreases with increasing phosphorylation of the membranes and becomes only slightly uncoupled by ionophores and less inhibited by dicyclohexylcarbodiimide (DCCD), diethylstilbestrol (DES), NO₃⁻ and vanadate. The inhibitory effect of phosphorylation is greater on the NO₃⁻-sensitive H⁺-ATPase activity than on the vanadate-sensitive activity. Restoration of H⁺-ATPase activity is achieved by allowing the phosphorylated membranes to dephosphorylate either in the absence or presence of exogenous alkaline phosphatase. Moreover, the presence of fluphenazine during the Ca²⁺/CaM-stimulated treatment inhibits membrane phosphorylation and protects the H⁺-ATPase activity from inhibition.     

A critical review on natural compounds interacting with the plant plasma membrane H+-ATPase and their potential as biologicals in agriculture

The plant plasma membrane (PM) H⁺-ATPase is an essential enzyme controlling plant growth and development. It is an important factor in response to abiotic and biotic stresses and is subject to tight regulation. We are in demand for new sustainable natural growth regulators and as a key enzyme for regulation of transport into the plant cell the PM H⁺-ATPase is a potential target for these. In this review, we have evaluated the known non-protein natural compounds with regulatory effects on the PM H⁺-ATPase, focusing on their mechanism of action and their potential as biologicals/growth regulators in plant production of future sustainable agriculture.