pH-optima in lipase-catalysed esterification

Though lipases are frequently applied in ester synthesis, fundamental information on optimal pH or substrate concentration, can almost only be found for the reverse reaction – hydrolysis. This study demonstrates that the pH-optima of lipase-catalysed esterifications differ significantly from the optima of the hydrolysis reaction. In the esterification of n-butanol and propionic acid with lipases of Candida rugosa (CRL) and Thermomyces lanuginosa (TLL) pH-optima of 3.5 and 4.25, respectively, were found. This is about 3–4 units (CRL) and 7 units (TLL) in pH lower than optimum for hydrolysis. Enzyme activity increased with increasing concentrations of protonated acid indicating that the protonated acid rather than the deprotonated form is substrate for esterification. The rate of esterification can be drastically increased by ensuring acid concentrations up to 1000 mmol L^?1 for CRL and 600 mmol L^?1 for TLL in the reaction system.     

Study of the thermal stability of D-amino acid oxidase from Trigonopsis variabilis reveals enzyme inactivation via multiple steps

The thermal stability of a highly purified preparation of D-amino acid oxidase from Trigonopsis variabilis (TvDAO), which does not show microheterogeneity due to the partial oxidation of Cys-108, was studied based on dependence of temperature (20-60°C) and protein concentration (5-100 µmol L^-1). The time courses of loss of enzyme activity in 100 mmol L^-1 potassium phosphate buffer, pH 8.0, are well described by a formal kinetic mechanism in which two parallel denaturation processes, partial thermal unfolding and dissociation of the FAD cofactor, combine to yield the overall inactivation rate. Estimates from global fitting of the data revealed that the first-order rate constant of the unfolding reaction (k _a) increased 10⁴-fold in response to an increase in temperature from 20 to 60°C. The rate constants of FAD release (k _b) and binding (k _-b) as well as the irreversible aggregation of the apo-enzyme (k _agg) were less sensitive to changes in temperature, their activation energy (E _a) being about 52 kJ mol^-1 in comparison with an E _a value of 185 kJ mol^-1 for k _a. The rate-determining step of TvDAO inactivation switched from FAD dissociation to unfolding at high temperatures. The model adequately described the effect of protein concentration on inactivation kinetics. Its predictions regarding the extent of FAD release and aggregation during thermal denaturation were confirmed by experiments. TvDAO is shown to contain two highly reactive cysteines per protein subunit whose modification with 5,5'-dithio-bis (2-nitrobenzoic acid) was accompanied by inactivation. Dithiothreitol (1 mmol L^-1) enhanced up to 10-fold the recovery of enzyme activity during ion exchange chromatography of technical-grade TvDAO. However, it did not stabilize TvDAO at all temperatures and protein concentrations, suggesting that deactivation of cysteines was not responsible for thermal denaturation.     

Biochemical properties of inulosucrase from Leuconostoc citreum CW28 used for inulin synthesis

Biochemical properties of inulosucrase from Leuconostoc citreum CW28, a potential biocatalyst for inulin synthesis, were determined in order to select optimal reaction conditions. The hydrolysis reaction was about 3.5 times more efficient than the transferase reaction. It was found that high sucrose concentrations (≈250 g L^-1) were required for maximum fructose transferase yields. High molecular weight inulin distributions were obtained with cell associated inulosucrase, while lower size products were associated to the activity of the free enzyme in solution. When using whole cells, mannitol was found as a by-product of the reaction resulting from the reduction of fructose released by sucrose hydrolysis. A 30 L pilot plant synthesis with 250 g L^-1 of sucrose was carried out using the cell associated inulosucrase resulting in 76% of the substrate being transformed to inulin.     

外源褪黑素与钙离子互作对高温胁迫下黄瓜幼苗过氧化伤害的缓解效应

为了探明褪黑素(MT)和钙离子(Ca²⁺)在调控植物耐热性中是否存在互作关系,以黄瓜幼苗为试材,分析了内源MT和Ca²⁺对高温胁迫的响应;并通过叶面喷施100 μmol·L^-1 MT、10 mmol·L^-1 CaCl₂、3 mmol·L^-1乙二醇二乙醚二胺四乙酸(EGTA,Ca²⁺螯合剂)+100 μmol·L^-1 MT、0.05 mmol·L^-1氯丙嗪(钙调素拮抗剂,CPZ)+100 μmol·L^-1 MT、100 μmol·L^-1氯苯丙氨酸(p-CPA,MT合成抑制剂)+10 mmol·L^-1 CaCl₂和去离子水(H₂O),研究高温下(42/32 ℃)外源MT和Ca²⁺对黄瓜幼苗活性氧积累、抗氧化系统及热激转录因子(HSF)和热激蛋白(HSPs)等的影响。结果表明: 黄瓜幼苗内源MT和Ca²⁺均受高温胁迫诱导;外源MT可上调常温下钙调素蛋白(CaM)、钙依赖蛋白激酶(CDPK5)、钙调磷酸酶B类蛋白(CBL3)、CBL结合蛋白激酶(CIPK2)mRNA表达;CaCl₂处理的MT合成关键基因色氨酸脱羧酶(TDC)、5-羟色胺-N-乙酰转移酶(SNAT)和N-乙酰-5-羟色胺甲基转移酶(ASMT)水平也显著升高,MT含量快速增加。MT和CaCl₂可显著增强高温下黄瓜的抗氧化能力,减少活性氧(ROS)积累,同时上调HSF7、HSP70.1和HSP70.11 mRNA表达,从而减轻高温胁迫引起的过氧化伤害,植株热害症状明显减轻,热害指数和电解质渗漏率显著降低。加入EGTA和CPZ后,MT对黄瓜幼苗抗氧化能力和热激蛋白表达的促进效应明显减弱,Ca²⁺对高温下黄瓜幼苗过氧化伤害的缓解效应也被p-CPA逆转。可见,MT和Ca²⁺均可诱导黄瓜幼苗的耐热性,二者在热胁迫信号转导过程中存在互作关系。     

基于FvCB模型分析盐分胁迫对棉花叶片光合作用的影响

为深入理解叶片光合特性对盐胁迫的响应机理,以棉花为试验材料,设置5个盐分(NaCl)浓度处理:0(CK)、50、100、150和200 mmol·L^-1,利用FvCB模型分析盐胁迫对棉花幼苗叶片光合特性的影响。结果表明:与CK相比,50和100 mmol·L^-1盐分处理增加了棉花叶片的最大羧化速率(V_{c max})和最大电子传递速率(J_max),但150和200 mmol·L^-1盐分处理显著降低了V_{c max}和J_max。叶片净光合速率(P_n)、叶肉导度(g_m)和暗呼吸速率(R_d)随盐分浓度升高而下降;与CK相比,50和100 mmol·L^-1盐分处理对g_m无显著影响,但P_n和R_d显著降低。150和200 mmol·L^-1盐分处理明显降低了P_n、g_m和R_d,且与0、50和100 mmol·L^-1盐分处理间存在显著差异;利用FvCB模型模拟了不同盐分胁迫下叶片净光合速率。与不考虑g_m的模拟结果相比,考虑g_m提高模拟值和实测值间的决定系数,并降低了平均绝对误差。棉花幼苗耐盐阈值为100～150 mmol·L^-1,随盐分浓度的增加,光合限制因素由叶肉因素转变为光合机构受损;引入g_m可以提高FvCB模型的模拟精度。     

不同钙浓度对宽叶雀稗幼苗的生长和抗性生理的影响

研究不同钙浓度对宽叶雀稗(Paspalum wettsteinii)幼苗生长和生理的影响, 对于揭示宽叶雀稗对不同钙浓度环境的适应机理至关重要。该研究采用盆栽砂培试验, 研究不同钙浓度(0、5、25、50、100和200 mmol·L^-1 CaCl₂)和不同处理时间(7、14、21和28天)对宽叶雀稗幼苗生长、渗透调节物质含量、抗氧化酶活性、叶绿素含量和光合参数的影响。结果表明, 随着CaCl₂浓度的增加和处理时间的延长, 宽叶雀稗幼苗株高等形态指标、生物量、渗透调节物质含量、抗氧化酶活性、叶绿素含量和光合参数呈先增后减的趋势, 低钙浓度(5-50 mmol·L^-1)环境下, 株高、叶长、叶宽、根长和生物量与对照(0 mmol·L^-1)相比均升高, 脯氨酸、可溶性蛋白和可溶性糖含量、过氧化物酶、过氧化氢酶和超氧化物歧化酶活性提高, 丙二醛含量和胞间CO₂浓度降低、叶绿素含量增加以及净光合速率、蒸腾速率和气孔导度增强; 高钙浓度(200 mmol·L^-1)环境下, 脯氨酸、可溶性蛋白和可溶性糖含量、过氧化物酶、过氧化氢酶和超氧化物歧化酶活性降低, 丙二醛含量和胞间CO₂浓度增加, 叶绿素含量减少以及净光合速率、蒸腾速率和气孔导度减弱。结合隶属函数分析, 低钙盐浓度(5-50 mmol·L^-1)处理对宽叶雀稗幼苗无抑制作用, 说明宽叶雀稗对低钙浓度具有一定的耐受性; 而在高钙浓度(200 mmol·L^-1)下, 宽叶雀稗幼苗通过提高自身有机渗透调节物质含量、增强酶活性、增加叶绿素含量以及增强光合作用等方式来快速调节植物生理代谢功能, 进而适应高钙浓度环境条件。     

Kinetics and substrate specificity of the glycanase activity associated with particles of Klebsiella bacteriophage No. 13

There is a glycanase activity associated with the particles of Klebsiella bacteriophage No. 13 which catalyzes hydrolysis of O-β-d-glucopyranosyl-(1 → 4)-β-d-mannopyranose linkages in Klebsiella serotype 13 capsular polysaccharide. The initial glycanase reaction velocity (at 37° and the optimum pH of 7–8) exhibits hyperbolical dependence on low concentrations of substrate, with K_m = 170 μm (in repeating units), and V_max = 140 nmol/min (glucose equivalents, for 10¹⁰ plaque-forming units). The reaction is inhibited by reaction products (type-13 penta- and decasaccharides, one and two repeating-units), and also by the substrate at concentrations above 1mm. Of seventy-four heterologous Klebsiella, and two other bacterial capsular heteropolysaccharides, as well as two substrate derivatives tested, only the Klebsiella serotype-2, -22, and -37 glycans were also depolymerized by the phage-13 enzyme. The reacting polysaccharides consist of repeating units, characteristically containing (a) chain 3eq,1eq → 4eq,1eq dihexopyranosyl sequences around the susceptible linkages, with equatorial hydroxyl and hydroxymethyl groups at C-2 and C′-5 next to them, and (b) branch carboxyl groups that may have to be located within a certain distance from these linkages.     

介质pH缓冲系统选择及其对龙须菜生长的影响

该文选择红藻门大型植物龙须菜(Gracilaria lemaneiformis)作为研究对象,通过黑白瓶法筛选出有机试剂POPSO(哌嗪-N,N-双(2-羟基乙烷磺酸)),能较好地缓冲室内龙须菜培养中介质pH的波动。在此基础上,探讨了POPSO对龙须菜生长的影响,结果表明:15 mmol·L ^-1及以上浓度的POPSO能较好地稳定介质pH值,减少系统中DIC浓度的急剧变化,但POPSO对CO₂浓度波动不起作用;试验结果还表明,介质中的CO₂浓度与龙须菜的生长速率间存在着类似酶动力学方程的关系,当介质中的CO₂浓度下降到5.25 μmol·L ^-1以下时,龙须菜生长出现抑制现象。相对稳定pH的培养环境,更有利于介质DIC中的HCO^-₃、CO^2-₃向CO₂的转换,缓解龙须菜生长的C抑制。     

Biocatalyst engineering exerts a dramatic effect on selectivity of hydrolysis catalyzed by immobilized lipases in aqueous medium

It has been found that enantioselectivity of lipases is strongly modified when their immobilization is performed by involving different areas of the enzyme surface, by promoting a different degree of multipoint covalent immobilization or by creating different environments surrounding different enzyme areas. Moreover, selectivity of some immobilized enzyme molecules was much more modulated by the experimental conditions than other derivatives. Thus, some immobilized derivatives of Candida rugosa (CRL) and C. antarctica-B (CABL) lipases are hardly enantioselective in the hydrolysis of chiral esters of (R,S)-mandelic acid under standard conditions (pH 7.0 and 25°C) (E<2). However, other derivatives of the same enzymes exhibited a very good enantioselectivity under nonstandard conditions. For example, CRL adsorbed on PEI-coated supports showed a very high enantio-preference towards S-isomer (E=200) at pH 5. On the other hand, CABL adsorbed on octyl-agarose showed an interesting enantio-preference towards the R-isomer (E=25) at pH 5 and 4°C. These biotransformations are catalyzed by isolated lipase molecules acting on fully soluble substrates and in the absence of interfacial activation against external hydrophobic interfaces. Under these conditions, lipase catalysis may be associated to important conformational changes that can be strongly modulated via biocatalyst and biotransformation engineering. In this way, selective biotransformations catalyzed by immobilized lipases in macro-aqueous systems can be easily modulated by designing different immobilized derivatives and reaction conditions.     

模拟昆虫取食对牛膝菊防御特征的影响

为了解入侵植物牛膝菊的入侵机理,研究其应对昆虫取食的响应,在开花前喷洒不同浓度(5、10、20 mmol·L-1)的茉莉酸甲酯(MeJA)来模拟不同程度的昆虫取食,试验结束时测定其株高、叶片数、花序数、生物量、比叶面积、叶上表皮毛密度,以及叶和花序中的缩合单宁、总酚、黄酮含量.结果表明:5 mmol·L-1 MeJA处...     

Generation of lipase-containing static emulsions in silicone spheres for synthesis in organic media

Because of the broad versatility of lipases as biocatalysts, interest has for some years been focused on the improvement of the economy of processes using these enzymes, especially by appropriate immobilisation. In this study, a method was developed to emulsify aqueous solutions of lipase A of Candida antarctica (CALA) and lipase of Thermomyces lanuginosa (TLL) in silicone elastomers yielding elastic beads. The persistent water-organic interface created by this static emulsion enabled an improved performance of the immobilised lipases due to the well known fact that from a kinetic point of view these enzymes show a higher efficiency in biphasic than in monophasic systems. The entrapped lipases catalysed the esterification of octanol and caprylic acid in hexane with an activity that, related to the free enzyme, was enhanced about 31-fold for CALA and 250-fold for TLL. Comparison to the activity of the same enzymes in sol–gels revealed that for CALA immobilisation in static emulsion was the only method yielding active biocatalysts, whereas activation of TLL was in the same range in static emulsion and sol–gels. However, apparent activity of TLL in static emulsion was considerably higher than in sol–gels due to the feasible high enzyme loading. The results indicate that immobilising lipases as static emulsion is a technique suitable for biotechnological application. Moreover, a transfer to enzymes of other classes seems possible.     

解脂假丝酵母(Candida lipolytica)对铜的吸附

研究了解脂假丝酵母的表面特性及培养时间、pH值、铜浓度、菌体投加量、吸附时间等因素对铜吸附的影响,并探讨了吸附动力学特征。结果表明,菌体表面可能有-OH和-PO₄^3-,培养96 h的菌体吸附性能最佳,适宜pH为4.0-6.0,适宜菌体投加量为25.0g·L^-1(湿重)。在初始浓度为20mg·L^-1的铜溶液中投加25.0g·L^-1(湿重)的菌体,吸附2h,铜的去除率最高达86.5%。铜浓度为5,10mg·L^-1时,铜的去除率高达95%以上。动力学分析表明,在实验设定的浓度范围内解脂假丝酵母对铜的吸附基本符合Freundlich吸附模型。红外光谱分析表明吸附后-OH吸收峰蓝移18cm^-1,其它吸收峰没有明显的变化。     

卵孢金孢藻对不同磷化合物的利用及生长响应

为了解水华蓝藻卵孢金孢藻对水体不同磷化合物的利用能力,试验以磷酸氢二钾为对照,通过室内模拟的方法探究不同磷基质条件下卵孢金孢藻的生长响应.结果表明: 卵孢金孢藻能直接利用三聚磷酸钠和十水焦磷酸钠,且对三聚磷酸钠有极高的利用率.15天后,三聚磷酸钠处理组的藻细胞生物量和叶绿素a浓度最高,分别达到(426.96±47.42) mg·L^-1和(1852.34±116.60) μg·L^-1.2-氨基乙基膦酸和五水β-甘油磷酸钠处理组生物量与对照无明显差异,可溶性无机磷变化特征响应了碱性磷酸酶活性大小,表明卵孢金孢藻能通过酶水解利用这两种有机磷.而整个培养过程中,草甘膦处理组可溶性无机磷浓度趋近于0 mg·L^-1,藻细胞生物量、比生长速率、叶绿素a浓度及光合活力均显著低于对照,表明草甘膦不仅不利于藻细胞摄取磷,还对其生长产生抑制作用.本研究结果为了解卵孢金孢藻向不同水生态系统的扩散机理提供了新的思路,对我国新型蓝藻水华的防治具有一定的理论参考价值.     

表面活性剂、酸雨和Cd2+复合污染对蚕豆胚根细胞核的毒性

用蚕豆根尖微核技术研究了Cd²⁺单因子以及与表面活性剂、模拟酸雨复合污染时对植物细胞的毒性作用.结果表明,Cd²⁺浓度在0～10.0mg·L^-1范围内,对蚕豆胚根细胞微核的形成有强烈的诱导作用,Cd²⁺浓度6.0mg·L^-1时的细胞微核率为13.85‰,对照组的微核率为4.53‰,此时污染影响指数(PI)为3.06;当环境中存在表面活性剂LAS1.0mg·L^-1或pH值降到4.5和3.5时,同一Cd²⁺浓度下,蚕豆根尖细胞微核率、PI降低,同时伴有核变形,细胞中颗粒物增多,胚根组织不容易分散等症状,根的生长受到抑制,说明表面活性剂、酸雨对Cd²⁺的毒性有协同作用.pH3.5的酸雨环境中Cd²⁺对蚕豆细胞的损伤程度比pH4.5酸雨环境高.在检测高浓度、强毒性污染物的致突变效应时,应作至少3个稀释倍数,找出蚕豆根尖细胞最高微核率及PI.     

车桑子幼苗生物量分配与叶性状对氮磷浓度的响应差异

调整叶性状和生物量分配格局是植物适应环境变化的主要途径, 研究车桑子(Dodonaea viscosa)幼苗生物量分配与叶性状对氮磷浓度的响应对认识车桑子在氮磷浓度变化下的适应策略具有重要意义。该研究通过砂培法, 测定不同氮浓度(3、5、15、30 mmol·L^-1)与不同磷浓度(0.25、0.5、1、2 mmol·L^-1)下车桑子幼苗的生长、生物量分配、叶性状的响应特征及其相互关系。结果表明: 高浓度氮(30 mmol·L^-1)促进了车桑子幼苗生长、叶片氮含量和生物量积累, 其余氮添加条件(3、5、15 mmol·L^-1)下车桑子幼苗各性状无显著差异, 但相比高氮水平, 其生物量积累和叶片氮含量显著降低, 根冠比和氮利用效率显著增加。随着磷添加浓度的增加, 车桑子幼苗生物量显著增加, 低磷条件(0.25、0.5 mmol·L^-1)限制了车桑子幼苗生长和生物量积累, 其根冠比和磷利用效率均没有发生显著变化, 但比叶面积和叶/茎生物量比例显著增加, 叶干物质含量显著降低。氮处理下, 叶片氮含量与根冠比显著负相关; 磷处理下, 叶片氮含量与比叶面积显著正相关。同时, 氮处理下, 车桑子幼苗株高、基径、总生物量等生长性状均与根冠比显著负相关, 与叶片氮含量显著正相关, 表明根冠比和叶片氮含量的调整在车桑子适应氮限制中发挥重要作用; 而磷处理下, 株高、基径、总生物量与比叶面积显著负相关, 与叶干物质含量显著正相关, 表明叶片结构性状的调整在车桑子适应低磷环境中具有重要意义。该研究表明, 车桑子幼苗生物量分配和叶性状及性状间的权衡策略对氮、磷的响应具有明显差异性, 在今后的研究中, 应关注氮和磷对植物性状影响的差异性。     

Different responses of biomass allocation and leaf traits of Dodonaea viscosa to concentrations of nitrogen and phosphorus

调整叶性状和生物量分配格局是植物适应环境变化的主要途径, 研究车桑子(Dodonaea viscosa)幼苗生物量分配与叶性状对氮磷浓度的响应对认识车桑子在氮磷浓度变化下的适应策略具有重要意义。该研究通过砂培法, 测定不同氮浓度(3、5、15、30 mmol·L^-1)与不同磷浓度(0.25、0.5、1、2 mmol·L^-1)下车桑子幼苗的生长、生物量分配、叶性状的响应特征及其相互关系。结果表明: 高浓度氮(30 mmol·L^-1)促进了车桑子幼苗生长、叶片氮含量和生物量积累, 其余氮添加条件(3、5、15 mmol·L^-1)下车桑子幼苗各性状无显著差异, 但相比高氮水平, 其生物量积累和叶片氮含量显著降低, 根冠比和氮利用效率显著增加。随着磷添加浓度的增加, 车桑子幼苗生物量显著增加, 低磷条件(0.25、0.5 mmol·L^-1)限制了车桑子幼苗生长和生物量积累, 其根冠比和磷利用效率均没有发生显著变化, 但比叶面积和叶/茎生物量比例显著增加, 叶干物质含量显著降低。氮处理下, 叶片氮含量与根冠比显著负相关; 磷处理下, 叶片氮含量与比叶面积显著正相关。同时, 氮处理下, 车桑子幼苗株高、基径、总生物量等生长性状均与根冠比显著负相关, 与叶片氮含量显著正相关, 表明根冠比和叶片氮含量的调整在车桑子适应氮限制中发挥重要作用; 而磷处理下, 株高、基径、总生物量与比叶面积显著负相关, 与叶干物质含量显著正相关, 表明叶片结构性状的调整在车桑子适应低磷环境中具有重要意义。该研究表明, 车桑子幼苗生物量分配和叶性状及性状间的权衡策略对氮、磷的响应具有明显差异性, 在今后的研究中, 应关注氮和磷对植物性状影响的差异性。     

三个乡土树种对Cu、Pb胁迫的生理生态响应

选择三种乡土树种樟树、大头茶和红鳞蒲桃,喷洒含有不同浓度的Cu和Pb溶液,同时设置一个没有喷洒重金属的空白实验.设置的浓度梯度Cu为0 mg·L^-1、50 mg·L^-1、150 mg·L^-1、250 mgL^-1;Pb为0 mg·L^-1、10 mg·L^-1、20 mg·L^-1、30 mg·L^-1.培育期结束后测量三个树种的树高;根、茎、叶的生物量和总生物量;以及叶片生物膜的透性和SOD的活性.结果表明(1)随着重金属浓度的增加,三种乡土树种的高生长和生物量的增加都受到了显著的抑制,浓度越高抑制越明显.相较而言红鳞蒲桃长势较好.(2)随着Cu、Pb浓度的升高,植物叶片的质膜透性变强,受到的伤害增大.Cu250 mg·L^-1下樟树叶片生物膜受到伤害最大,而在Pb30 mg·L^-1下大头茶叶片质膜受到伤害最大.(3)SOD活性在Cu的胁迫下呈现随着浓度的增加,先升高后下降的规律,但大头茶的SOD活性在一直增加.(4)在Pb的胁迫下,SOD的活性随胁迫的浓度的升高一直下降,只有红鳞蒲桃在后期表现出了增长的趋势.     

外生菌根真菌通过调节离子平衡提高蒙古栎耐盐性

为探究盐胁迫对蒙古栎生长的影响以及外生菌根真菌(ECMF)对蒙古栎离子平衡的调节作用,对蒙古栎幼苗接种4种ECMF(铆钉菇、褐环乳牛肝菌、厚环粘盖牛肝菌和美味牛肝菌)后,以1年生非菌根化与菌根化幼苗为试验材料,进行36 d的NaCl胁迫(0、100、200、300 mmol·L^-1)处理,分析幼苗的菌根特征、生长量、叶伤害症状、叶片电解质渗透率及含水量、根茎叶离子含量的变化特征。结果表明: 4种ECMF均能与蒙古栎建立共生体系,菌根化幼苗的根系较非菌根化幼苗粗壮。盐胁迫下,蒙古栎幼苗的生长受到抑制并出现焦叶症状,其叶片质膜损伤和失水程度随盐胁迫浓度升高而加重。低盐胁迫时(100 mmol·L^-1),蒙古栎优先将Na⁺积累在根和茎中,中高浓度盐胁迫下(200～300 mmol·L^-1),根成为积累Na⁺的首要器官。ECMF通过增加根部的Na⁺水平和减少茎、叶的Na⁺积累,加强对K⁺和Ca²⁺的吸收以提高K⁺/Na⁺和Ca²⁺/Na⁺,进而调节蒙古栎的离子平衡。4种ECMF对蒙古栎盐毒害的缓解作用存在差异,铆钉菇作用效果最好,褐环乳牛肝菌次之,厚环粘盖牛肝菌和美味牛肝菌的作用相对较小。     

对羟基苯甲酸胁迫下褪黑素对黄瓜胚根生理生化特性的影响

以‘津研四号’黄瓜为试材,分别用0、2.5、5、7.5、10、12.5、15、17.5、20 mmol·L^-1浓度的对羟基苯甲酸(PHBA)溶液对黄瓜种子处理72 h,选出胁迫作用较明显的10 mmol·L^-1浓度;再分别用0、1、10、25、50、75、100 μmol·L^-1的褪黑素(MT)溶液对10 mmol·L^-1 PHBA下的黄瓜种子预处理24 h,72 h后观察MT的缓解效果.结果表明: 缓解PHBA胁迫效果最明显的MT浓度为75 μmol·L^-1.随着PHBA浓度的升高,黄瓜种子胚根伸长的抑制作用明显增加;用10、25、50、75、100 μmol·L^-1的MT预处理PHBA胁迫下的黄瓜种子均能不同程度缓解PHBA胁迫对胚根的抑制作用,其中以75 μmol·L^-1的MT缓解效果最好.用MT预处理黄瓜种子可显著提高PHBA胁迫下黄瓜种子中淀粉酶活性及胚根中超氧化物歧化酶、过氧化物酶、过氧化氢酶和抗坏血酸过氧化物酶活性,并降低胚根中O₂^-·的产生速率及H₂O₂和丙二醛含量.外源MT能够通过降低氧化胁迫和促进淀粉的分解转化来降低PHBA对黄瓜发芽的影响.