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1.
油菜素内酯和脱落酸调控葡萄果实花色苷合成的研究   总被引:1,自引:0,他引:1  
【目的】为研究2,4-表油菜素内酯(2,4-epibrassinolide,EBR)和脱落酸(abscisic acid,ABA)处理对葡萄花色苷合成与可溶性固形物含量、果皮苯丙氨酸解氨酶(PAL)和类黄酮糖基转移酶(UFGT)活性以及果实内源ABA含量的影响,探索油菜素内酯调控葡萄果实成熟及花色苷合成的机理。【方法】以酿酒葡萄‘赤霞珠’(Cabernet Sauvignon)和‘烟73’(Yan 73)为试材,在葡萄转色前分别用0.1、0.4、0.8 mg.L-1EBR,1mg.L-1Brz(brassinazole,BR生物合成抑制剂)和200 mg.L-1ABA,均匀喷施于葡萄果实,在葡萄成熟过程中测定葡萄果皮花色苷含量及PAL和UFGT酶活性,同时测定果实ABA和可溶性固形物含量。【结果】在果实着色初期,‘赤霞珠’和‘烟73’葡萄果皮PAL和UFGT活性及果实内源ABA含量均逐渐升高,当果实接近成熟花色苷含量基本稳定时ABA含量开始降低。与对照相比,0.4mg.L-1EBR和200 mg.L-1ABA处理显著增加了果实内源ABA含量,提高了果皮PAL和UFGT活性,促进了果皮花色苷的合成和果实可溶性固形物的积累。0.1 mg.L-1和0.8 mg.L-1EBR处理总体增加了果实内源ABA含量,促进了花色苷的合成和可溶性固形物的积累,并提高了UFGT和PAL酶活性,但比0.4 mg.L-1EBR处理提高的幅度小,且差异显著。1 mg.L-1Brz处理使果实ABA的合成推迟,果实可溶性固形物含量、果皮PAL和UFGT活性以及花色苷含量均低于对照,但差异不显著。【结论】外源EBR和ABA处理促进了葡萄成熟和花色苷合成,在不同浓度EBR处理中,以0.4 mg.L-1处理效果较好;内源ABA可能参与了EBR对葡萄成熟和花色苷合成的调控。  相似文献   

2.
1-甲基环丙烯对高温下香蕉果实后熟的影响   总被引:3,自引:0,他引:3  
以香蕉果实为试材,研究了1-甲基环丙烯(1-MCP)对高温逆境下香蕉果实后熟生理的影响。结果表明:35℃高温下贮藏的香蕉果实出现了明显的青皮熟现象,而0.5μL/L的1-MCP处理24h后可显著抑制高温下贮藏果实硬度的降低,延缓果皮细胞膜透性的升高,同时有效地延迟了果肉中淀粉酶活性升高、淀粉含量下降及可溶性糖含量上升。1-MCP处理果实于35℃下贮藏9d后移入20℃环境,进一步延缓了这些后熟生理变化。1-MCP和高温均抑制了果皮叶绿素含量下降,因此1-MCP处理减轻了香蕉热害的程度,延长了果实在高温下的贮藏寿命。  相似文献   

3.
采用外源过氧化氢(H2O2)、能诱导植物产生内源H2O2的茉莉酸甲酯(MJ)和水杨酸(SA)处理采后香蕉果实,探讨H2O2在采后香蕉果实耐冷诱导中的作用,结果表明:在7℃下贮藏,外源20 mmol·L-1 H2O2、0.7 mmol·L-1 SA、0.1mmol·L-1 MJ处理能使果实冷害症状推迟2~5d出现;处理还延缓了香蕉果皮细胞膜透性和MDA含量的增加,提高了超氧化物歧化酶(SOD)和过氧化物酶(POD)活性,抑制了过氧化氢酶(CAT)活性,从而导致香蕉果皮H2O2积累。推测H2O2可能作为信号分子参与诱导了采后香蕉果实的抗冷性。  相似文献   

4.
温度逆境胁迫可以诱导热激蛋白的表达,而热激处理能够减轻果实冷害。为了探讨温度逆境对香蕉热激蛋白基因表达的调控、辨析香蕉热激蛋白基因的表达与果实冷害的关系,采用同源序列法分离了香蕉果皮HSP70基因序列-根据已经报道的HSP70基因的氨基酸保守序列设计引物、以香蕉果皮总RNA为模板,用RT-PCR方法克隆香蕉的HSP70 cDNA,Northern杂交分析该基因在不同贮藏温度下的表达特征。结果得到2个序列不同的HSP70基因片段,分别命名为Ma-HSP70-1和Ma-HSP70-2,Ma-HSP70-1和Ma-HSP70-2之间的碱基同源性为86.9%,氨基酸同源性为97.1%。Northern杂交的结果表明,38℃短期热激处理诱导了Ma-HSP70-2基因的表达,低温冷藏能使2个基因的表达增强。并初步认为Ma-HSP70可能与香蕉果实耐冷性有关。  相似文献   

5.
过氧化氢在香蕉果实采后耐冷性诱导中的作用   总被引:4,自引:0,他引:4  
采用外源过氧化氢(H2O2)、可诱导植物产生内源H2O2的茉莉酸甲酯(MJ)和水杨酸(SA)处理香蕉果实,探讨H2O2在香蕉果实采后耐冷诱导中的作用。结果表明:在7℃下贮藏,外源20mmol·L-1H2O2、0.7mmol·L-1SA、0.1mmol·L-1MJ处理能使果实冷害症状推迟2~5d出现;延缓了香蕉果皮细胞膜透性和MDA含量的增加,提高了超氧化物歧化酶(SOD)和过氧化物酶(POD)活性,抑制了过氧化氢酶(CAT)活性,从而使果皮中H2O2积累。推测H2O2可能作为信号分子参与诱导了香蕉果实采后的抗冷性。  相似文献   

6.
以北五味子为试材,在转色期分别用400mg/L乙烯利和1 000mg/L脱落酸(ABA)处理果实,研究乙烯利和ABA对北五味子木脂素及苯丙氨酸解氨酶(PAL)活性的影响。结果表明:转色期至成熟处理,对照果实总木脂素和PAL活性均呈增加的变化趋势,成熟期果实总木脂素乙烯利和ABA处理比对照分别提高11.08%和15.11%,处理间无显著差异,与对照差异显著;CK成熟期果实PAL活性为20.21U·h-1·g-1,乙烯利和脱落酸对提高北五味子果实总木脂素含量和增加PAL活性具有促进作用,乙烯利和ABA处理的果实PAL活性分别为22.09、22.36U·h-1·g-1,处理间差异不显著。  相似文献   

7.
外源脱落酸对巨玫瑰葡萄着色及浆果品质的影响   总被引:4,自引:0,他引:4  
本文以避雨栽培巨玫瑰葡萄为试验材料,在转色期用脱落酸(ABA)溶液100 mg/L、500mg/L和1 000mg/L处理果穗,并对成熟过程中果皮花色苷含量、果汁可溶性固性物含量(TSS)、可滴定酸含量和pH值进行了测定。结果表明,三种浓度ABA处理均能促进果皮的着色和果实成熟,但却抑制果汁可溶性固形物含量提高和单粒重的快速增加。其中,ABA 500mg/L处理在显著提高巨玫瑰葡萄果皮中的花色苷含量,降低可滴定酸含量的同时,其可溶性固形物超过上市的最低质量标准,并且能使葡萄果实提早10天成熟,整体上提高了果实品质。  相似文献   

8.
甜瓜幼苗耐冷性相关生理指标的综合评价   总被引:1,自引:0,他引:1  
【目的】明确10个生理指标与甜瓜幼苗耐冷性的关系。【方法】以26份耐冷性差异明显的甜瓜种质为试材,分别测定在低温处理后各种质幼苗的电导率、丙二醛含量、叶绿素含量、可溶性糖含量、可溶性蛋白含量、游离脯氨酸含量、根系活力、POD活性、SOD活性、CAT活性等10个低温逆境相关的生理指标,采用基本统计量比较、灰色关联分析、相关分析、主成分分析等方法对耐冷性进行综合评价。【结果】在室内4℃低温处理48 h后种质间冷害指数差异最大,且达到极显著水平,不同种质之间各生理指标差异显著。其中丙二醛、游离脯氨酸、可溶性糖、可溶性蛋白和叶绿素含量及电导率与耐冷性密切相关,具有较高的关联度和相关系数,且在主成分分析中对耐冷性的贡献率较大。基于这6个生理指标数据,聚类分析能将耐冷性不同的种质区别开。【结论】10个生理指标可简化为6个指标,即丙二醛、游离脯氨酸、可溶性糖、可溶性蛋白和叶绿素含量及电导率,其中游离脯氨酸、可溶性糖和可溶性蛋白含量可优先作为甜瓜耐冷性的评价指标,用于甜瓜耐冷性育种研究。  相似文献   

9.
香蕉果实贮藏冷害与NAD激酶活性变化的关系   总被引:2,自引:0,他引:2  
刘彩霞  顾采琴  朱冬雪 《园艺学报》2008,35(10):1425-1430
 以‘巴西'香蕉果实为试材,研究了果实采后在22℃和6℃下贮藏期间NAD激酶(NADK)活性与冷害发生情况,膜渗透性,丙二醛(MDA)含量,多酚氧化酶(PPO)以及苯丙氨酸解氨酶(PAL)活性变化的关系。结果表明,6℃下贮藏3d 时果实出现冷害症状, 11d时冷害加重,同时NAD激酶活性、膜渗透性、MDA含量和PPO活性均始终高于22℃贮藏的, 并在11d时达到高峰,而PAL活性则呈下降趋势,其活性始终低于22℃贮藏的。6℃下用NAD激酶激活剂氯化钙处理香蕉果实后,NADK受到激活,冷害程度加重,而用钙离子通道阻塞剂异博定(verapamil,Vp)处理后则抑制了NADK 活性,果实冷害症状延迟4 d 出现,冷害程度减弱,说明香蕉果实冷害发生与NADK 活性变化密切相关。  相似文献   

10.
为明确"南天黄"香蕉果实的催熟浓度、温度等条件,为生产上催熟提供技术参考.以"南天黄"香蕉果实为试材,比较1、0.8、0.5g/L乙烯利处理后,14、18、22℃贮藏对果实后熟进程、果皮色度、果肉硬度和可溶性固形物含量等变化的影响.结果表明,随着乙烯利浓度及贮藏温度提高,香蕉果实色差H值和硬度下降速度及可溶性糖含量增加...  相似文献   

11.
Calcium-dependent protein kinase (CDPK) is an important Ca2+ sensor in plant development and responses to stress stimuli. Banana fruit is a typical climacteric- and chilling-sensitive fruit. The roles of CDPK genes in the ripening and chilling response of banana fruit are unclear. We isolated a cDNA fragment with full-length coding MaCDPK7 (HM061075) from fruit peel tissue. Induction of MaCDPK7 expression in fruit peel was observed 0.5 h after phytohormone ethylene treatment, earlier than the up-regulation of MaACO1 and MaACS1, coding a 1-aminocyclopropane-1-carboxylate oxidase and 1-aminocyclopropane-1-carboxylate synthase, respectively. Penetration of calcium signaling blockers, EGTA, or LaCl3 inhibited the ripening and gene expression of MaCDPK7, MaACO1, and MaACS1 in the in vitro cultured peel pieces, but Ca2+ application removed the inhibitory effect of EGTA and LaCl3. This suggested that MaCDPK7 might be a positive regulator involved in the calcium signaling in banana fruit ripening. Under temperature stresses, we found that MaCDPK7 gene expression increased 3 h after hot water dipping (HWD). The HWD-treated fruits exhibited markedly less chilling injury (CI) than control fruits in cold storage. Stored at 7°C (CI temperature) dramatically increased MaCDPK7 gene expression, while pre-treatment of HWD repressed the induction in cold storage. These results show that the MaCDPK7 gene is involved in regulating banana fruit ripening and chilling resistance induced by heat treatment.  相似文献   

12.
低温和多效唑对香蕉及大蕉超氧物歧化酶和脱落酸的影响   总被引:28,自引:0,他引:28  
周碧燕  梁立峰 《园艺学报》1995,22(4):331-335
低温胁迫处理引起香蕉和大蕉超氧物歧化酶(SOD)活性的下降,香蕉下降的幅度比大蕉大。大蕉在低温胁迫下脱落酸(ABA)含量增加,而香蕉ABA含量明显低于大蕉,并在低温胁迫过程中出现波动。多效唑处理可以提高香蕉的抗冷性,低温胁迫条件下处理香蕉比对照的香蕉具有较高SOD活性和内源ABA含量。香蕉和大蕉SOD同工酶谱带组成在低温前后没有变化,但香蕉谱带中多数强度有所改变,其中同工酶V强度明显加强,大蕉SOD同工酶则相对较稳定。  相似文献   

13.
Cucumber chilling-resistant cultivar Changchun mici and -sensitive cultivar Beijing jietou were used in this study to investigate the effects of exogenous PAs on protection against chilling injury as well as on changes of physiological features, and the fluctuation of free PAs content in the leaves under chilling stress. Upon chilling treatment, free spermidine (Spd), spermine (Spm) and putrescine (Put) were remarkably induced in the leaves of cv. Changchun mici 1 day after treatment. The induction of Put declined thereafter, whereas Spd and Spm levels increased steadily. In the leaves of cv. Beijing jietou, Put content was increased only at 1 day after chilling while Spd content decreased significantly upon chilling treatment. Chilling reduced soluble protein content, and decreased the activities of antioxidant enzymes, including superoxidase dismutase (SOD), peroxidase (POD), catalase (CAT) and ascorbate peroxidase (APX) only in Beijing jietou. However, these changes could be renovated by exogenous application of Put and Spd. It was also found that pretreatment with Put and Spd diminished the increased electrolyte leakage and malondialdehyde (MDA) content caused by chilling in the leaves of both cultivars. Pretreatment of methyglyoxal-bis-(guanylhydrazone) (MGBG), the PAs biosynthetic inhibitor cancelled the effects of PAs in most of the treatments. Moreover, histochemical staining and quantitative measurements showed that exogenous application of Put and Spd eliminated but MGBG exaggerated the hydrogen peroxide (H2O2) accumulation caused by chilling stress, especially in leaves of Beijing jietou. Interestingly, Changchun mici was found to contain higher endogenous free PAs contents compared to Beijing jietou. While no significant difference of SOD, POD and CAT activities was found between non-chilling Changchun mici and Beijing jietou seedlings, the former exhibited higher APX activity than the latter. These results suggest that PAs play important roles in the tolerance of cucumber against chilling stress, which is most likely achieved by acting as oxidative machinery against chilling injury.  相似文献   

14.
为提高吸胀冷害下菜豆种子发芽率,缓解吸胀冷害对菜豆种子的伤害。以低温敏感型菜豆"热那亚"种子为试材,设置CK(常温对照)、LT(4℃低温处理)和LT+Put(4℃低温处理时加入1 mmol·L^-1的腐胺(Put))3个处理,研究外源Put对吸胀冷害下菜豆种子萌发及抗性的影响。结果表明:吸胀冷害下,外源Put处理后LT+Put组菜豆种子发芽率、发芽指数和种子活力与LT组相比分别提高了87.12%、124.21%和191.99%;LT+Put与LT处理相比细胞膜透性下降,可溶性物质含量增加,抗氧化酶活性升高,O2^-、H2O2和MDA含量增加。说明外源Put的施用可能通过降低细胞膜透性,增加可溶性物质含量,诱导抗氧化酶活性,直接或间接调节ROS清除系统来提高菜豆种子对吸胀冷害的抗性,提高菜豆种子的发芽率、发芽指数和种子活力。  相似文献   

15.
Irradiation of green banana fruit (Musa AAA, Cavendish subgroup, ‘Williams’) with an ultraviolet (UV)-C fluence of 720 Jm'2 increased ethylene evolution five-fold compared with controls during the first 24 h in either dark or light. The activity of phenylalanine ammonia-lyase (PAL) in extracts from the outer peel of irradiated fruit increased at least two-fold in either light or dark, but at 20°C it took 1-2 d for PAL activity to increase above the rate in controls. Irradiation did not affect the content of total phenolic compounds in outer peel in either dark or light until 4-6 d later. The content of chlorogenic acid was also not increased in either dark or light by UV-C. The catechin content of outer peel doubled in the dark within 24 h of irradiation and continued to increase six-fold during the first three days after irradiation. Exposure to white light (13.2 Wm 2) after irradiation almost completely prevented this increase in catechin content. These results show a close metabolic relationship between catechin and the bronze pigment previously reported in bananas irradiated with UV-C.  相似文献   

16.
华盛顿脐橙果实采后油胞病害与酶活性的相关性   总被引:1,自引:0,他引:1  
以华盛顿脐橙果实为试验材料,研究采后果皮油胞病害的发生状况及病变过程中果皮POD(过氧化物酶)、PPO(多酚氧化酶)、PAL(苯丙氨酸解氨酶)等相关酶活性的变化,以探索柑橘果皮油胞的病变生理。研究结果表明,果皮油胞病害发生率随贮藏时间的增加而上升;伤果的发病率显著增加,发病时间早;低温降低了贮藏后期果皮油胞病变率。损伤处理显著提高了果皮PPO、POD和PAL酶活性,而低温则抑制了这些酶活性。在整个常温贮藏过程中,正常果和损伤果的油胞病害发生率与这3种酶活性都呈显著和极显著正相关。说明果皮POD、PPO和PAL的高活性是果皮油胞病变的重要生理因素。  相似文献   

17.
研究了冷藏、ABA、1-MCP、热处理及HCl护色等采后处理对桂味荔枝果皮花色素苷含量和花色素苷酶活性变化的影响。结果表明,与冷藏适温(3℃)相比,0℃下果实遭受了冷害,果皮花色素苷酶活性急剧增强,峰值提前出现,花色素苷含量迅速减少。ABA、1-MCP处理能暂时延缓花色素苷酶活性的上升。热水处理不同程度地诱导了果实花色素苷酶活性的升高,果皮褪色,而适当浓度的酸处理能显著抑制花色素苷酶活性,对果皮具有较好的护色效果。  相似文献   

18.
为了明确李果实花青苷合成的调控因子,以安哥诺李为试材,对果皮花青苷、内源激素和PAL、PPO活性的变化以及内源激素、酶活性与花青苷的相关性进行研究。结果表明,果皮花青苷含量在发育前期含量很低,发育后期含量迅速升高,呈上升趋势;果皮中ABA、乙烯、ZT含量和PPO活性与花青苷的变化趋势相同,乙烯释放量与花青苷呈极显著正相关关系r=0.8885**,ABA和ZT含量与花青苷呈显著正相关关系r=0.7159*和r=0.7476*,PPO活性未达显著水平;果皮中IAA、GA3含量和PAL活性变化在发育前期含量较高,在发育后期含量较低,果实发育过程中IAA、GA3含量呈逐渐下降趋势,与花青苷呈显著负相关关系r=-0.7039*和r=-0.8238*,PAL活性未达显著水平。  相似文献   

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