Ca2+、ABA预处理蝴蝶兰类原球茎的脱水保护系统比较及信号传导关系

CaCl2和ABA溶液及两者联合分别预处理蝴蝶兰类原球茎(PLB)后脱水,对比PLB脱水前后的成活率、脱水保护系统指标变化及Ca2+与ABA信号传导关系.结果表明,CaCl2和ABA溶液及两者联合预处理均能明显提高PLB脱水后的成活率.CaCl2和ABA溶液对可溶性糖、蔗糖、还原糖、SOD和总抗氧化能力有相同的效应趋势,对可溶性蛋白、热稳定蛋白含量及POD、CAT活性的作用趋势有所差异.ABA溶液提高PLB耐脱水性的能力被胞质Ca2+ 螯合剂BAPTA/AM 和钙调蛋白拮抗剂氯丙嗪所削弱,Ca2+预处理提高PLB耐脱水能力被ABA合成抑制剂环丙嘧啶醇削弱.在蝴蝶兰PLB的耐脱水性诱导中,Ca2+和ABA具有基本相同的生理生化基础,在信号传递中两者互相关联,CaCl2取代ABA用于提高PLB耐脱水性是可行的.     

花生种子耐脱水力的形成与可溶性糖累积的关系

花生胚轴的耐脱水力在40－65DAP的发育后期逐渐增加,同时胚轴还原性糖／非还原性糖比值下降。缓慢干燥可同时诱导35DAP胚轴累积蔗糖与寡糖（水苏糖与棉籽糖）;外源ABA及高渗处理可诱导35DAP离体胚轴累积蔗糖,但不能累积寡糖（水苏糖）。耐脱水胚轴可溶性糖成分的模拟混合物可在水活度0．32及零上温度进入玻璃态;而不耐脱水胚轴的可溶性糖模拟混合物仅在零下温度进入玻璃态。模拟实验证明在干燥状态下可溶性糖与花生2S蛋白结合,并消除了2S蛋白的干燥结晶。     

细茎石斛拟原球茎生长与有效成分积累的关系

目的：研究细茎石斛拟原球茎生长规律及其与两种有效成分总生物碱和可溶性多糖积累的关系。方法：采用液体静止培养方法培养细茎石斛拟原球茎,在一个周期(60天)内,每隔10天取样,测定拟原球茎的鲜、干重,总生物碱含量和可溶性多糖含量。结果：液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型,拟原球茎经过10d左右的延迟期后进入对数生长期,第50d左右达到生长高峰,此后．生长缓慢．进入静止期。拟原球茎中总生物碱和可溶性多糖含量随着拟原球茎的生长逐渐积累,在培养的第40d左右达到高峰,之后含量有所下降,这两种有效成分的积累与生长基本同步,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量。结论：液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型,总生物碱和可溶性多糖的积累与生长基本同步,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量。     

细茎石斛拟原球茎生长与有效成分积累的关系

目的 :研究细茎石斛拟原球茎生长规律及其与两种有效成分总生物碱和可溶性多糖积累的关系。方法 :采用液体静止培养方法培养细茎石斛拟原球茎 ,在一个周期 ( 60天 )内 ,每隔 1 0天取样 ,测定拟原球茎的鲜、干重 ,总生物碱含量和可溶性多糖含量。结果 :液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型 ,拟原球茎经过 1 0d左右的延迟期后进入对数生长期 ,第 5 0d左右达到生长高峰 ,此后 ,生长缓慢 ,进入静止期。拟原球茎中总生物碱和可溶性多糖含量随着拟原球茎的生长逐渐积累 ,在培养的第 40d左右达到高峰 ,之后含量有所下降 ,这两种有效成分的积累与生长基本同步 ,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量。结论 :液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型 ,总生物碱和可溶性多糖的积累与生长基本同步 ,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量     

水杨酸对霍山石斛类原球茎细胞生长及多糖合成的影响

本研究考察了水杨酸对霍山石斛类原球茎悬浮培养细胞生长、多糖合成、碳代谢的影响,并研究了细胞生长、多糖合成以及蔗糖消耗的动力学。结果表明,水杨酸对霍山石斛类原球茎细胞生长有轻微的抑制作用,但能够显著改善类原球茎对碳源的利用,提高胞内可溶性糖的含量,从而促进多糖的合成,其中以添加100μmol/L浓度的水杨酸效果最好,培养18d时,多糖产量达到3.129g/L,为对照的1.63倍。建立的培养动力学模型能较好地反映水杨酸调控霍山石斛类原球茎悬浮培养过程中细胞生长、多糖合成和蔗糖消耗特性。     

精胺对霍山石斛类原球茎悬浮培养细胞生长和多糖合成的影响

研究了在添加外源精胺时,霍山石斛类原球茎细胞生长、多糖积累、主要营养物质消耗以及细胞内多胺含量的变化。结果表明,0.6mmol/L的精胺明显促进霍山石斛类原球茎细胞的生长和多糖的合成。细胞的比生长速率从0.046d-1提高到0.054d-1。培养30d时,类原球茎干重达32.4gDW/L,多糖总产量为2.46g/L,分别是对照的1.32和1.31倍。添加外源精胺能够提高内源多胺的含量,同时,蔗糖酶和硝酸还原酶等相关代谢酶的活性增强,促进了碳、氮的吸收和利用。     

锗对霍山石斛类原球茎悬浮培养细胞生长和多糖合成及氧化还原态的影响

为解决霍山石斛类原球茎液体培养细胞生长缓慢和代谢水平低下的问题,研究了不同浓度的锗(GeO2)对霍山石斛类原球茎增殖、多糖合成及碳氮利用的影响,分析了类原球茎细胞内还原糖、可溶性蛋白质含量、抗氧化酶活性以及细胞氧化还原态的变化。结果表明,适当浓度的二氧化锗(4.0mg/L)显著促进霍山石斛类原球茎的增殖和多糖的积累,最大细胞干重为32.6g/L,最大多糖产量为3.78g/L;显著提高胞内还原糖和可溶性蛋白质含量,超氧化物歧化酶和过氧化氢酶的活性明显升高,而过氧化物酶的活性则有所降低;氧化还原态分析发现,二氧化锗处理的细胞内还原型谷胱甘肽/氧化型谷胱甘肽的值明显提高,谷胱甘肽还原酶活性升高。添加适量的二氧化锗有利于细胞生长和多糖合成。     

褐飞虱侵害后不同水稻品种根及叶片脱落酸含量的变化

为了解褐飞虱Nilaparvata lugens （Stål）侵害后水稻耐虫性与植物体内源激素关系,应用酶联免疫吸附法（enzyme-linked immunosorbent assay, ELISA）研究褐飞虱若虫侵害分蘖期超级培矮64S/E32和TN1,灌浆期协优963和TN1后根及叶片脱落酸（abscisic acid, ABA）含量变化.结果表明：褐飞虱侵害分蘖期超级培矮64S/E32和TN1后3 d,叶片ABA含量显著上升,ABA含量根冠比（根ABA/叶片ABA）显著下降;侵害后6 d,超级培矮64S/E32叶片ABA含量显著下降,根冠比显著上升;但TN1叶片ABA含量在褐飞虱侵害后3 d和6 d显著上升,根冠比显著下降.褐飞虱侵害灌浆期协优963与分蘖期超级培矮64S/E32变化一致,TN1在褐飞虱侵害后3 d叶片ABA含量显著上升,根冠比显著下降;侵害后6 d,叶片ABA含量、ABA含量根冠比均显著上升.由ABA含量变化百分比可见,分蘖期ABA含量变化幅度较灌浆期大;耐虫品种变化幅度较感虫品种大,持续期较感虫品种短;叶片变化幅度较根部大.褐飞虱侵害后,两种不同生育期两种抗性不同的水稻品种比较,耐虫品种叶片ABA含量先上升（3 d）后下降（6 d）,ABA含量根冠比先下降（3 d）后上升（6 d）;感虫品种叶片ABA含量持续上升（3 d和6 d）,分蘖期ABA含量根冠比持续下降（3 d和6 d）,灌浆期ABA含量根冠比先下降（3 d）后上升（6 d）;耐、感虫水稻品种根部变化规律不明显.这些差别表明不同水稻（耐虫和感虫）品种受褐飞虱侵害后体内ABA含量变化规律不同.本研究结果对深入阐明水稻耐虫品种的机制具有重要参考价值.     

霍山石斛类原球茎二步法培养细胞生长和多糖合成的动力学研究

磷是调控类原球茎细胞生长和多糖积累的有效因素。为了获得较高的多糖产量,根据霍山石斛类原球茎生长和多糖积累的动力学特性,提出了二步培养方式,采用了补料策略,研究了其培养过程的动力学特性,并建立了相关模型。结果表明,采用二步法培养,生物量从28.7g DW/L提高到44.2g DW/L, 多糖产量从1.86g/L提高到5.22g/L,多糖含量从6.4%提高到11.9%。建立的模型基本反映了类原球茎生长和多糖积累的动力学机制。     

低温和外源NO对铁皮石斛原球茎多糖合成的影响

以铁皮石斛(Dendrobium officinale)原球茎为材料,研究了低温(4℃)、外源NO(NO供体SNP)以及NO清除剂(cPTIO)和一氧化氮合酶抑制剂(PBITU)对铁皮石斛原球茎中NO含量、蔗糖合成酶(SS)活性、多糖含量以及蔗糖、果糖、葡萄糖等糖含量的影响,以明确低温和內源NO在多糖合成中的关系。结果显示:(1)4℃低温处理下,铁皮石斛原球茎中NO含量显著上升,SS活性升高,蔗糖、果糖和葡萄糖含量增加,多糖含量也得到提高;SNP(0.5mmol·L-1)处理与4℃低温处理具有相似的效果;且低温诱导的铁皮石斛原球茎中SS活性提高和多糖含量的增加时期均在NO大量产生之后、蔗糖的积累早于果糖和葡萄糖。(2)4℃低温+SNP组合处理能够显著提高铁皮石斛原球茎中SS活性、NO含量以及蔗糖、果糖、葡萄糖和多糖含量,它们分别比对照组显著高出了68.04%,96.20%,60.69%、45.64%、66.90%和67.03%,且比低温和SNP单独处理效果都好。(3)PBITU能够部分抑制低温诱发铁皮石斛原球茎中产生NO,抑制率达到77.15%;同时还抑制了低温对铁皮石斛原球茎中SS活性、多糖合成和蔗糖、果糖、葡萄糖积累的促进作用。(4)SNP+cPTIO和4℃+cPTIO处理组中铁皮石斛原球茎SS活性和蔗糖、果糖、葡萄糖、多糖含量及NO水平,且与对照组差异不显著。研究表明,低温和外源NO对铁皮石斛原球茎多糖的合成均具有促进作用,并且低温可诱导铁皮石斛原球茎产生NO,SS活性提高和多糖含量增加与NO产生相关,说明NO是诱导铁皮石斛原球茎多糖合成所必需的信号分子。     

Physiological changes in gentian axillary buds during two-step preculturing with sucrose that conferred high levels of tolerance to desiccation and cryopreservation

BACKGROUND AND AIMS: Induction of dehydration tolerance is a key to achieving high survival rates in cryopreservation of plant specimens. It has been reported previously that two-step preculturing with sucrose effectively increased desiccation tolerance in axillary buds of gentian (Gentiana scabra), which allow the buds to survive cryopreservation. This study is aimed at characterizing each step of this preculturing and to elucidate physiological changes induced during this preculturing. METHODS: In standard two-step preculture, excised gentian axillary buds were incubated for 11 d on MS medium with 0.1 m sucrose at 25 degrees C (first step: mild osmotic stress was given) and the subsequent incubation on MS medium with 0.4 m and 0.7 m sucrose for 1 d each (second step). The levels of abscisic acid (ABA), proline and soluble sugars in gentian buds during the preculture were determined. Effects of various combinations of two-step preculturing and of exogenous ABA and proline were studied. KEY RESULTS: During the first preculture step, there was a transient increase in ABA content peaking on day 4, which declined to a background level at the end of the first and second step preculturing. Proline level increased steadily during the first preculture step and increased further in the second preculture step. Incubating buds with medium containing proline, instead of the two-step preculturing, did not allow them to survive desiccation. Incubating buds with ABA instead of 0.1 m sucrose-preculturing effectively increased desiccation tolerance only when it was followed by the second preculture step. Fluridone, an ABA synthesis inhibitor included in the two-step preculture medium, reduced desiccation tolerance of the buds. The normal first-step preculture increased the levels of soluble sugars 2.4-fold, especially sucrose and raffinose. Buds treated with the second preculture step had greatly increased sucrose levels. CONCLUSIONS: These observations lead to the hypothesis that the first preculture step involves ABA-mediated cellular changes and the second step induces loading of sucrose in the gentian buds.     

Accumulation of soluble sugars, heat-stable proteins and dehydrins in cryopreservation of protocorm-like bodies ofDendrobium candidumby the air-drying method

Protocorm-like bodies (PLBs) of Dendrobium candidum were successfully cryopreserved by the air-drying method. The optimal water content before freezing seemed to be at the range of 0.1 g H₂O/g DW (11 % on fresh weight basis) to 0.5 g H₂O/g DW (33 % on fresh weight basis). Changes in soluble sugars, heat-stable proteins and dehydrins during desiccation of PLBs were analyzed. Extensive accumulation of soluble sugars was observed at water content of about 7.2 g H₂O/g DW (after 24 h desiccation), and the sugars content did not increase further during the following desiccation. The amount of heat-stable protein increased significantly when water content decreased to 1.0 g H₂O/g DW (after approximately 66 h desiccation). Results from immunological detection showed that two bands of the heat-stable proteins with respective molecular masses of 28.7 and 34.3 kDa were dehydrins which appeared when water content dropped to 1.0 g H₂O/g DW. Therefore, it seemed that accumulation of dehydrins happened later than that of soluble sugars. Interestingly, exogenous ABA treatment of PLBs before desiccation could also induce the accumulation of soluble sugars, heat-stable proteins and dehydrins. The possible roles of these substances in the acquisition of dehydration and freezing tolerance were discussed.     

Differential effects of abscisic acid on desiccation tolerance and carbohydrates in three species of liverworts

Tissues of three species of in vitro grown liverworts, Riccia fluitans, Pallavicinia lyellii, and Marchantia polymorpha, were subjected to rapid drying with and without preculture for 1 week on medium containing 10 μM ABA. ABA preculture initiated total desiccation tolerance in R. fluitans, whereas control tissues were killed after 30 min of drying. Survival was also improved in P. lyellii, whereas ABA did not affect survival of M. polymorpha after rapid drying. ABA treatment did, however, reduce the rate of water loss in M. polymorpha. Total soluble carbohydrates were increased in ABA-treated R. fluitans and P. lyellii, but not in M. polymorpha, although there was no correlation between survival and changes in the percentage of these carbohydrates as reducing sugars. These differences in response to ABA and desiccation likely reflect different adaptations of these three species to conditions in situ.     

Cryopreservation of protocorm-like bodies (PLBs) of <Emphasis Type="Italic">Phalaenopsis bellina</Emphasis> (Rchb.f.) christenson by encapsulation-dehydration

Protocorm-like bodies (PLBs) of Phalaenopsis bellina were successfully cryopreserved by the encapsulation-dehydration approach. Various stages in obtaining successful cryopreservation using this method were optimized. Encapsulated PLBs precultured in half-strength MS medium supplemented with 0.75 M sucrose for 3 days exhibited the highest viability in terms of 2,3,5-triphenyltetrazoliumchloride (TTC) reduction. The amount of sucrose in the PLBs after incubation in different concentrations of sucrose for different periods of time determined by HPLC. The highest sucrose concentration was 7 mg/g of PLBs for the PLBs treated with 0.75 M sucrose for 3 days as compared to the control which had only 1 mg/g sucrose. After sucrose preculture, the PLBs were subjected to desiccation using one of two methods. Desiccation using silica gel was more efficient in reducing PLBs moisture content. After 6 h of desiccation, PLBs desiccated using laminar air flow had 43.5% moisture content while for those desiccated using silica gel had 32% moisture content. PLBs desiccated to different moisture contents were plunged into LN. After storage in LN the encapsulated PLBs were re-warmed. Two weeks after re-warming PLBs viability was determined by TTC reduction and re-growth assessed. Encapsulated PLBs precultured with 0.75 M sucrose for 3 days followed by desiccated using silica gel for 5 h resulting in a moisture content of 39% lead to the highest post re-warming viability in terms of TTC reduction (46.6% of control PLBs) and 30% re-growth.     

Acquisition of desiccation tolerance by isolated maize embryos exposed to different conditions: the questionable role of endogenous abscisic acid

The effect of exogenous ABA on acquisition of desiccation tolerance has been well documented for the embryos of several species. including maize ( Zea mays L.). It has also been suggested that endogenous ABA plays a role in regulating the same phenomena. To test this hypothesis, endogenous ABA was quantified by radioimmunoassay. Our results show that: (1) during embryogenesis in maize, endogenous ABA increase-concomitantly with the acquisition of desiccation tolerance: (2) ABA deficient embryos of the vp 5 mutant are desiccation intolerant, but tolerance can he induced by exogenous ABA: and (3) desiccation tolerance is acquired if desiccation sensitive embryos undergo a slow drying treatment, during which ABA increases. However, when embryos were preincubated in fluridone to prevent ABA accumulation during slow drying, desiccation tolerance was induced in spite of the low level of endogenous ABA in the embryo. Our results cast doubts on an exclusive role of ABA in the acquisition of desiccation tolerance in maize embryo.     

A simple method for cryopreservation of <Emphasis Type="Italic">Ginkgo biloba</Emphasis> callus

Two-years-old Ginkgo biloba cell culture initiated from cotyledonary explants was cryopreserved by a simple desiccation method. Preliminary incubation of callus clumps on MS preculture medium supplemented with 100 g l⁻¹ sucrose and 2 mg l⁻¹ ABA for 7 and 14 days resulted in accumulation of endogenous soluble sugars and was essential for cell culture post-cryopreservation survival. The optimal time for the preculture on sucrose-and-ABA containing medium was found to be 14 days. The sufficient desiccation duration was determined as 150 min. FCM profiles of calli maintained for 2 years remained stable and were not affected by cryopreservation.     

板栗种子发育期间ABA等生理指标与脱水耐性的相关性研究

对板栗种子发育期间胚轴和子叶中部分生理指标的变化以及它们与板栗种子脱水耐性的相关性进行研究.结果表明:随着板栗种子不断发育,在花后80 d胚轴和子叶中ABA、淀粉、可溶性蛋白质量分数同步达到最大值,可溶性糖质量分数达到最低,此时板栗种子的脱水耐性最强,可确定为板栗的最佳采收期.另外,通过相关分析可知,板栗种子在发育期间...     

Development of Desiccation Tolerance during Embryogenesis in Rice (Oryza sativa) and Wild Rice (Zizania palustris) (Dehydrin Expression,Abscisic Acid Content,and Sucrose Accumulation)

The ability of seeds to withstand desiccation develops during embryogenesis and differs considerably among species. Paddy rice (Oryza sativa L.) grains readily survive dehydration to as low as 2% water content, whereas North American wild rice (Zizania palustris var interior [Fasset] Dore) grains are not tolerant of water contents below 6% and are sensitive to drying and imbibition conditions. During embryogenesis, dehydrin proteins, abscisic acid (ABA), and saccharides are synthesized, and all have been implicated in the development of desiccation tolerance. We examined the accumulation patterns of dehydrin protein, ABA, and soluble saccharides (sucrose and oligosaccharides) of rice embryos and wild rice axes in relation to the development of desiccation tolerance during embryogenesis. Dehydrin protein was detected immunologically with an antibody raised against a conserved dehydrin amino acid sequence. Both rice and wild rice embryos accumulated a 21-kD dehydrin protein during development, and an immunologically related 38-kD protein accumulated similarly in rice. Dehydrin protein synthesis was detected before desiccation tolerance had developed in both rice embryos and wild rice axes. However, the major accumulation of dehydrin occurred after most seeds of both species had become desiccation tolerant. ABA accumulated in wild rice axes to about twice the amount present in rice embryos. There were no obvious relationships between ABA and the temporal expression patterns of dehydrin protein in either rice or wild rice. Wild rice axes accumulated about twice as much sucrose as rice embryos. Oligosaccharides were present at only about one-tenth of the maximum sucrose concentrations in both rice and wild rice. We conclude that the desiccation sensitivity displayed by wild rice grains is not due to an inability to synthesize dehydrin proteins, ABA, or soluble carbohydrates.     

自然干旱胁迫下长春花叶片和根部的激素和可溶性糖代谢变化

植物在离开生长环境较短时间内（1~6 h）会导致缓慢的表面水分散失,引起自然的干旱胁迫。本文以耐旱植物长春花（Catharanthus roseus）为材料,研究其在离土干旱胁迫中的脱落酸（ABA）及可溶性糖含量变化。结果表明,长春花根部ABA含量在正常条件下低于叶片中的含量,干旱胁迫促进了ABA在根部的积累,6 h时增加至最高值。蔗糖酸性转化酶活性可能受到ABA的诱导在胁迫6 h时最高,比对照高出30%左右。长春花叶片中总可溶性糖含量在对照条件下非常稳定,但在干旱胁迫过程中,其随着时间的延长呈现线性增加的趋势（r²=0.964）,蔗糖和已糖含量在胁迫过程中也呈增加的趋势,可能发挥着渗透调控节功能。     

Desiccation tolerance in Physcomitrella patens: Rate of dehydration and the involvement of endogenous abscisic acid (ABA)

The moss Physcomitrella patens , a model system for basal land plants, tolerates several abiotic stresses, including dehydration. We previously reported that Physcomitrella patens survives equilibrium dehydration to ?13 MPa in a closed system at 91% RH. Tolerance of desiccation to water potentials below ?100 MPa was only achieved by pretreatment with exogenous abscisic acid (ABA). We report here that gametophores, but not protonemata, can survive desiccation below ?100 MPa after a gradual drying regime in an open system, without exogenous ABA. In contrast, faster equilibrium drying at 90% RH for 3–5 days did not induce desiccation tolerance in either tissue. Endogenous ABA accumulated in protonemata and gametophores under both drying regimes, so did not correlate directly with desiccation tolerance. Gametophores of a Ppabi3a/b/c triple knock out transgenic line also survived the gradual dehydration regime, despite impaired ABA signaling. Our results suggest that the initial drying rate, and not the amount of endogenous ABA, may be critical in the acquisition of desiccation tolerance. Results from this work will provide insight into ongoing studies to uncover the role of ABA in the dehydration response and the underlying mechanisms of desiccation tolerance in this bryophyte.