外源赤霉素和多效唑对芍药冬季鳞芽发育的影响

以目前芍药(Paeonia lactiflora)主栽品种‘紫凤羽’为供试材料,在冬季用300 mg·L~(-1)赤霉素(GA_3)及其延缓剂多效唑(PP_(333))进行灌根处理,待对照组进入蕾期对PP_(333)处理组施以300 mg·L~(-1) GA_3作解除处理,每隔10 d对各处理组鳞芽取样,测定其超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性以及丙二醛(MDA)、可溶性蛋白、可溶性糖、内源玉米素(ZT)、赤霉素(GA_3)、脱落酸(ABA)、吲哚乙酸(IAA)、乙烯(ETH)、多胺等的含量,采用石蜡切片对鳞芽发育状态进行观察,对各处理组鳞芽出土日期、出芽率、成花率、花期及株高进行观察统计。结果表明:外源GA_3会加快抗氧化酶活性变化速度,降低MDA含量,提高可溶性糖及可溶性蛋白的积累及利用,促进亚精胺(Spd)积累,在鳞芽发育初期提高了内源GA_3及ZT含量,在后期降低了其含量,内源IAA、ABA、ETH的含量也呈降低趋势,缩短了花瓣原基(petal primordium)分化期,促进了鳞芽发育进程,而PP_(333)与之相反,延长了花瓣原基分化期,抑制鳞芽发育;试验数据显示高浓度GA_3、ZT利于鳞芽发育启动,低浓度GA_3、ZT、IAA、ABA、ETH利于启动后的发育进程,且内源多胺调控芍药鳞芽发育时,其中Spd起主导作用。本文旨在为芍药花期调控提供参考依据,以期根据市场需求制定芍药花期的综合调控方案。     

叶面喷施PP_(333)和6-BA对甜荞花芽分化及内源激素的影响

以甜荞品种‘北早生’和‘赤甜荞1号’为材料,利用多效唑(PP_(333))和6-苄基腺嘌呤(6-BA)在不同幼苗时期进行叶片喷施处理,并采用扫描电镜观察花芽分化过程,记录开花时间,调查开花和结实数,通过液质联用方法检测3种内源激素生长素(IAA)、赤霉素(GA_3)、脱落酸(ABA)及人工合成细胞分裂素(6-BA)含量,探究两种植物生长调节剂对甜荞的花芽分化及内源激素含量的影响,为甜荞花期调控提供依据。结果显示:(1)第二片真叶期喷施100mg·L~(-1)PP_(333)和150mg·L~(-1)6-BA能显著提高甜荞结实率和单株产量,两种处理的结实率分别较对照提高49.5%、39.4%,单株产量分别提高41.8%、23.0%。(2)观察甜荞花芽分化过程并将其划分5个时期,分别为生长锥分化前期、生长锥分化期、小花原基分化期、雌雄蕊分化期和雌雄蕊形成期,在第二片真叶期喷施PP_(333)和6-BA均加快了甜荞花芽分化进程,使其开花时间提前。(3)喷施PP_(333)在幼苗期和现蕾期降低了内源IAA、6-BA含量,增加GA_3、ABA含量,而在盛花期增加内源IAA、6-BA含量,降低ABA、GA_3含量;喷施6-BA在幼苗期和现蕾期增加了内源GA_3、IAA含量,在盛花期降低了内源GA_3、IAA含量,3个时期均降低了内源ABA含量,增加了6-BA含量。研究发现,第二片真叶期是调控甜荞小花发育的关键时期,在此时叶面喷施100mg·L~(-1)PP_(333)和150mg·L~(-1)6-BA的调控效果最佳,可加快甜荞花芽分化进程,使开花时间提前,增加单株结实粒数,提高甜荞品种的结实率和单株产量;PP_(333)主要是通过减少甜荞开花数,增强弱势小花活力来提高结实粒数,而6-BA主要是利用增加开花数,提高有效可孕小花数来增加结实粒数。     

外源Spd预处理对甜瓜白粉病抗性及其内源多胺的诱导分析

以甜瓜感病品种‘0544’为试材,测定外源亚精胺(Spd)预处理和白粉病菌接种后甜瓜幼苗的光合参数、抗氧化酶活性、内源多胺含量及多胺合成与代谢相关基因表达等的变化,探讨外源Spd处理对甜瓜幼苗白粉病抗性的诱导作用机制。结果显示:(1)1.0mmol·L-1外源Spd处理可显著降低甜瓜幼苗的白粉病病情指数,缓解植株发病症状;(2)外源Spd处理可诱导甜瓜幼苗的多胺合成以及代谢相关基因(SAMDC、ADC、ODC、Spd、Spm、PAO)显著上调表达;(3)外源Spd处理可诱导甜瓜幼苗腐胺(Put)和Spd含量显著增加,而外源Spd并接种白粉病菌处理对甜瓜幼苗精胺(Spm)含量积累的诱导更加显著;(4)接种白粉病菌诱导了甜瓜幼苗的多酚氧化酶(PPO)、过氧化物酶(POD)和超氧化物歧化酶(SOD)的活性,外源Spd预处理后再接种白粉病的诱导作用更大,同时外源Spd处理还诱导了甜瓜幼苗过氧化氢(H_2O_2)含量的升高;(5)在观测期(120h)内,接种白粉病菌对甜瓜叶片的光合作用抑制较小,而外源Spd预处理并接种白粉病菌共同诱导了甜瓜幼苗的光合速率(Pn)、气孔导度(Gs)和蒸腾速率(Tr)的显著升高。研究认为,在外源Spd预处理甜瓜幼苗后再接种白粉病菌,甜瓜幼苗可以通过多胺的快速积累及代谢产生的H_2O_2来启动响应机制,进而通过增强防御酶活性等途径来提高对白粉病的抗性。     

外源GA3对紫斑牡丹幼苗叶片解剖结构与光合特性及内源激素含量的影响

以1年生紫斑牡丹幼苗为试验材料,采用不同浓度(0、100、300、500 mg/L)赤霉素(GA_3)喷施叶片处理,通过透射电镜、扫描电镜、光学显微镜观察幼苗叶片解剖结构,光合仪测定幼苗光合参数并以酶联免疫吸附法测叶片内源激素含量,探究外源GA_3对紫斑牡丹幼苗叶片解剖结构、光合特性和内源激素水平的影响。结果表明:(1)低浓度GA_3处理的紫斑牡丹叶肉细胞增大,栅栏组织外层细胞中叶绿体数量增加,高浓度GA_3处理则与之相反;GA_3处理叶片的栅栏组织/海绵组织比值(P/S)、组织结构紧密度(CTR)均下降,而其组织结构疏松度(SR)增加;GA_3处理的幼苗叶片的叶肉细胞内各叶绿体大小显著大于对照,随着GA_3处理浓度增加,紫斑牡丹叶肉细胞内叶绿体的体积趋于增大,类囊体垛叠凝聚逐渐松散,叶绿体上淀粉颗粒在300 mg/L GA_3处理中较明显;叶片气孔长度、宽度、气孔器大小、气孔开度和气孔密度随着GA_3浓度升高先升高后下降,同时叶片上表皮角质层厚度随GA_3浓度的升高而增加。(2)紫斑牡丹叶片净光合速率(P_n)、气孔导度(Cond)、蒸腾速率(T_r)、水分利用率(WUE)在100和300 mg/L GA_3处理下大都显著高于对照,且300 mg/L GA_3处理显著高于其余处理,而其在500 mg/L GA_3处理下显著低于对照。(3)紫斑牡丹叶片脱落酸(ABA)和吲哚乙酸(IAA)含量均在500 mg/L GA_3下显著高于对照,而在其余浓度处理下不同程度低于对照,叶片内源玉米素核苷(ZR)和GA_3含量均在300 mg/L GA_3处理下显著高于其余处理和对照,而其余处理相比对照均无显著变化;叶片的ZR/ABA、ZR/IAA、ZR/GA_3和(IAA+GA_3+ZR)/ABA比值都在300 mg/L GA_3处理下显著高于其他处理,叶片的IAA/ABA和ABA/GA_3比值均在500 mg/L GA_3处理下显著高于其他处理。研究发现,适宜浓度外源GA_3处理,能显著提高紫斑牡丹幼苗叶片光合速率、水分利用效率及蒸腾速率,调节植物体内源激素的含量及平衡,从而使叶片能合成较多有机物,促进幼苗生长。     

外源亚精胺对甜瓜幼苗白粉病抗性的影响

以高感白粉病甜瓜‘066’、感病品种‘0544’、抗病品种‘Yuntian-930’为试材,对白粉病菌胁迫下外源亚精胺（Spd）处理的甜瓜幼苗叶片超氧化物岐化酶（SOD）、过氧化物酶（POD）、过氧化氢酶（CAT）和多酚氧化酶（PPO）活性,以及过氧化氢（H₂O₂）、丙二醛（ MDA）和光合色素含量进行了研究,探讨外源Spd对甜瓜白粉病抗性的诱导效应及其生理机制。结果表明：（1）白粉病菌接种后甜瓜叶片的防御酶活性、光合色素含量先升后降,MDA含量升高;（2）外源Spd处理缓解了白粉病菌胁迫下甜瓜叶片防御酶活性、光合色素含量的下降,降低MDA含量及甜瓜的病情指数,并以1.0 mmol/L Spd处理效果最佳;（3）外源Spd处理使甜瓜叶片产生了更多的H₂O₂;（4）外源Spd提高甜瓜对白粉病抗性具有一定广谱性,且可向上传导。研究认为,H₂O₂可能参与白粉病胁迫下信号的传递,外源Spd可通过缓解白粉病菌胁迫下甜瓜防御酶活性和光合色素含量的下降来诱导甜瓜对白粉病的抗性。     

GA3浸种处理对五种晚花杜鹃种子萌发的影响

晚花杜鹃(late flower Rhododendron)是一类花期较晚的杜鹃品种,具有较高的观赏价值,被广泛应用于庭院种植和园林绿化。随着旅游以及经济发展的需要,开发和利用晚花杜鹃资源显得非常迫切。自然条件下晚花杜鹃萌发率相对较低,因此为提高晚花杜鹃萌发率,探究不同浓度赤霉素(GA_3)处理对五种杜鹃种子萌发的影响,该文以五种晚花杜鹃(小白杜鹃、大白杜鹃、桃叶杜鹃、长蕊杜鹃和九龙山杜鹃)为实验材料,通过不同浓度(0、300、400、500、600、700 mg·L~(-1))的GA_3对五种晚花杜鹃种子进行24 h浸种处理,测定其发芽指数、发芽势、发芽率以及成苗率等指标,分别确定五种杜鹃种子萌发的最适GA_3浓度,并对相同处理下五种杜鹃种子的萌发率和成苗率进行比较。结果表明:(1) GA_3浸种对五种晚花杜鹃种子萌发具有促进作用,在适当GA_3浓度下五种杜鹃种子的发芽指数、发芽势和发芽率均显著高于对照组,萌发时滞、萌发高峰期和持续萌发时间均较对照组浓度相对缩短。(2)大白杜鹃、桃叶杜鹃和九龙山杜鹃种子在GA_3浓度为600 mg·L~(-1)处理时各项萌发指标相对较好;长蕊杜鹃以GA_3浓度为700 mg·L~(-1)浸种处理萌发效果相对较好;小白杜鹃以GA_3浓度为400和700 mg·L~(-1)处理最好。因此,在杜鹃的栽培中,可以采用赤霉素GA_3处理法提高种子发芽率,缩短萌发时间。     

外源亚精胺对Ca(NO3)2胁迫下番茄幼苗光合特性和抗氧化酶活性的影响

以耐盐性较弱的番茄品种上海‘合作903’幼苗为试验材料,采用营养液栽培方法,研究了叶面喷施1mmol.L-1亚精胺(Spd)对75mmol.L-1 Ca(NO32)胁迫下番茄幼苗生长、叶绿素含量、光合及荧光参数、叶片抗氧化酶活性的影响,以探讨外源亚精胺缓解Ca(NO3)2胁迫伤害的机制。结果显示:Ca(NO3)2胁迫能够显著抑制番茄幼苗的生长;与Ca(NO32)胁迫处理相比,叶面喷施外源Spd 9d后,受胁迫番茄幼苗的株高、茎粗、干重、鲜重分别显著增加70.9%、15.8%、43.4%、41.4%;叶绿素a、b的含量分别提高17.7%、13.8%;净光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)、光合电子传递效率(rETR)和光化学猝灭系数(qP)分别升高6.6%、18.0%、31.0%、4.9%、5.0%,而胞间二氧化碳浓度(Ci)、非光化学猝灭系数(qN)分别降低21.5%、8.1%;超氧化物歧化酶(SOD)、过氧化氢酶(CAT)活性分别增加10.7%和37.5%,而丙二醛(MDA)含量和超氧阴离子(O2.-)产生速率分别显著下降34.5%、17.1%。研究表明,外源Spd通过提高番茄幼苗抗氧化酶活性来有效清除体内活性氧,维持光合机构的稳定性,提高其光合速率,从而缓解Ca(NO3)2胁迫对番茄幼苗的伤害。     

外源多胺对铜胁迫下水鳖叶片多胺代谢、抗氧化系统和矿质营养元素的影响

采用营养液水培的方法,研究了外源亚精胺(Spd)和精胺(Spm)对Cu胁迫下水鳖叶片3种形态多胺(PAs)、抗氧化系统及营养元素的影响。结果表明:(1)Cu胁迫使水鳖叶片腐胺(Put)急剧积累,Spd和Spm明显下降,从而使(Spd+Spm)/Put比值也随之下降。外源Spd和Spm显著或极显著逆转Cu诱导的PAs变化,抑制Put的积累,缓解Spd和Spm的下降,从而提高了(Spd+Spm)/Put比值。(2)外源Spd和Spm抑制了Cu胁迫诱导的多胺氧化酶(PAO)的增加,缓解了二胺氧化酶(DAO)的下降。(3)与单一Cu胁迫相比,Spd和Spm显著或极显著提高了超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)和谷胱甘肽还原酶(GR)活性和抗坏血酸(AsA)、谷胱甘肽(GSH)、游离脯氨酸(Pro)含量,从而降低了超氧阴离子(O2.-)产生速率和过氧化氢(H2O2)含量,极显著降低了丙二醛(MDA)含量,缓解了Cu诱导的氧化胁迫。(4)外源Spd和Spm显著或极显著缓解了Cu胁迫下矿质营养元素吸收平衡的紊乱。以上结果均说明了外施Spd和Spm可增加水鳖对Cu胁迫的耐受性。     

外源5-氨基乙酰丙酸对NaCl胁迫下酸枣光合特性的影响

以2年生酸枣幼苗为试验材料,探讨不同浓度NaCl(0、4、8、12g·kg-1)胁迫下喷施5-氨基乙酰丙酸(ALA,75、150mg·L~(-1))对酸枣光合特性的影响。结果显示:(1)不同浓度NaCl胁迫下,外源ALA对酸枣叶片的净光合速率(Pn)、胞间二氧化碳浓度(Ci)、气孔导度(Gs)、蒸腾速率(Tr)及叶绿素含量等具有明显促进作用。(2)在不同浓度NaCl胁迫下,喷施75mg·L~(-1)的ALA仅在NaCl浓度为4和8g·kg-1处理下对酸枣Tr值具有显著提高作用,而喷施150mg·L~(-1) ALA在各NaCl浓度胁迫下对其Pn、Ci和Tr均具有显著促进作用。(3)在重度NaCl胁迫(12g·kg-1)下,喷施150mg·L~(-1) ALA对酸枣叶片叶绿素含量具有显著提高作用,而喷施75mg·L~(-1)浓度ALA却无明显提高。研究表明,在NaCl胁迫条件下,外源ALA能有效改善酸枣叶片光合气体交换参数,提高叶绿素含量,从而缓解NaCl胁迫的伤害,提高其光合能力,并以喷施150mg·L~(-1) ALA的缓解效果更好。     

外源亚精胺对Hg2+胁迫下凤眼莲抗氧化系统的影响

通过Hoagland溶液培养实验,研究了外源亚精胺(Spd)(0.1 mmol?L-1)对Hg2+(0、10、20、30和40μmol?L-1)胁迫下凤眼莲叶片细胞内叶绿素、可溶性糖、可溶性蛋白含量及抗氧化系统的调节作用.结果显示,(1)随Hg2+处理浓度的升高,各处理凤眼莲叶片叶绿素a(Chl a)和叶绿素b(Chl b)含量均先升后降,并均在10μmol?L-1时达到最高值,但外源Spd处理组显著高于相应对照.(2)各处理凤眼莲叶片可溶性蛋白含量随Hg2+处理浓度的升高也呈先升后降趋势,而可溶性糖含量则呈持续上升趋势,但外源Spd处理亦明显高于相应对照.(3)随Hg2+处理浓度的升高,抗氧化物质AsA和GSH含量及抗氧化酶SOD、CAT、POD、APX及GR活性也均呈先升后降的变化趋势,而外源Spd处理植株的含量和活性均显著高于相应对照.(4)各处理凤眼莲叶片的H2O2、MDA含量及O2?-产生速率随Hg2+处理浓度的升高均持续上升,但在外源Spd处理后均比对照组下降.研究表明,Hg2+胁迫使凤眼莲生长受到严重伤害,外源Spd可大幅度地提高其抗氧化物质含量和保护酶活性,从而增强凤眼莲抗Hg2+胁迫的能力.     

Study on russet-related enzymatic activity and gene expression in ‘Shine Muscat’ grape treated with GA3 and CPPU

Physiological (metabolite analysis) and molecular (gene expression) approaches were used to understand the mechanism underlying russet formation in response to the application of GA₃ and CPPU (Forchlorfenuron) in a Japanese table grape cultivar ‘Shine Muscat’. Several different concentrations of GA₃ and GA₃?+?CPPU [25?mg?L^?1 GA₃ (A), 25?mg?L^?1 GA₃?+?5?mg?L^?1 CPPU (B), 25?mg?L^?1 GA₃?+?10?mg?L^?1 CPPU (C), and 25?mg?L^?1 GA₃?+?15?mg?L^?1 CPPU (D)] were applied to grape berry clusters at two weeks after flowering (WAF). No russet was observed on the berries treated with the ‘C’ combination. Lower levels of phenylalanine ammonia-lyase (PAL) activity was observed in the treated samples, relative to the untreated material. Reduced peroxide (POD) activity was also observed in response to different treatments, while the expression of Peroxidase 17 and Phenylalanine ammonia-lyase G1 genes mirrored lignin content. Increased activity of 4-coenzyme A ligase (4CL) may contribute to decreasing the level of russet and help to improve grape berry quality.     

Stem elongation and gibberellins in alpine and prairie ecotypes of Stellaria longipes

The potential for gibberellins (GAs) to control stem elongation and itsplasticity (range of phenotypic expression) was investigated inStellaria longipes grown in long warm days. Gibberellinmetabolism and sensitivity was compared between a slow-growing alpine dwarfwithlow stem elongation plasticity and a rapidly elongating, highly plastic prairieecotype. Both ecotypes elongated in response to exogenous GA₁,GA₄ or GA₉, but surprisingly, the alpine dwarf wasrelatively unresponsive to GA₃. Endogenous GA₁,GA₃, GA₄, GA₅, GA₈, GA₉and GA₂₀ were identified and quantified in stem tissue harvested atcommencement, middle and end of the period of most rapid elongation. Theconcentration of GAs which might be expected to promote shoot elongation washigher during rapid elongation than toward its end for both ecotypes. Whilethere was a trend for certain GAs (GA₃, GA₄,GA₉, GA₂₀) to be higher in stems of the alpine ecotypeduring rapid elongation, that result does not explain the slower growth of thealpine ecotype and the faster growth of the prairie ecotype under a range ofconditions. To determine if the two ecotypes metabolized GA₂₀differently, plants were fed [²H]- or[³H]-GA₂₀. The metabolic products identified included[²H₂]-GA₁, -GA₈, -GA₂₉,-GA₆₀, -3-epi-GA₁, GA₁₁₈(-1-epi-GA₆₀) and -GA₇₇. The concentration of[²H₂]-GA₁ also did not differ between the twoecotypes and metabolism of [²H₂]- or[³H]-GA₂₀ was also similar. In the same experiments thepresence of epi-GA₁, GA₂₉, GA₆₀,GA₁₁₈ and GA₇₇ was indicated, suggesting that these GAsmay also occur naturally in S. longipes, in addition tothose described above. Collectively, these results suggest that while stemelongation within ecotypes is likely regulated by GAs, differences in GAcontent, sensitivity to GAs (GA₃ excepted), or GA metabolism areunlikely to be the controlling factor in determining the differences seen ingrowth rate between the two ecotypes under the controlled environmentconditionsof this study. Nevertheless, further study is warranted especially underconditions where environmental factors may favour a GA:ethylene interaction.     

GA3 induced flowering in Podophyllum hexandrum Royle: A rare alpine medicinal herb

Podophyllum hexandrum Royle, an important alpine herb, is the source of highly valued podophyllotoxin. The effect of some plant growth substances (GA₃, BAP & ABA), uniconazole (an inhibitor of GA biosynthesis), and a combination of GA₃ and uniconazole were examined in respect to influence on sprouting in rhizomes of P. hexandrum and on induction of flowering at a lower altitude. Amongst the various chemicals tested, GA₃ had a marked effect resulting in uniform sprouting and also induced flowering in about half of the treated rhizomes. While BAP also promoted early sprouting, delayed sprouting was seen in rhizomes treated with ABA. Uniconazole treatment, either alone or with GA₃ was found to inhibit flowering and also resulted in reduced plant height. GA₃ treatment of rhizomes from plants that was maintained for up to 30 months at a lower altitude also induced flowering thus replacing the normal chilling requirement of plants. These results suggest that treatment of GA₃ could be effectively used for inducing uniform sprouting and flowering in rhizomes of P. hexandrum grown at lower altitudes.     

巨桉和天竺桂幼树对不同浓度SO2的光合生理响应

二氧化硫是大气主要污染物之一,可对植物的关键生理过程光合作用产生重要影响。利用密闭环境控制室熏气处理,研究不同浓度(自然状态下浓度、0.5mg·L-1、1.5mg·L-1、3.0mg·L-1)SO2对盆栽巨桉和天竺桂幼树叶绿素含量、光响应曲线、光合特征参数、光合日变化及硫含量的影响。结果表明:(1)SO2胁迫显著减少了巨桉叶绿素a、b含量,且叶绿素a/b值显著降低,而天竺桂在SO2胁迫下叶绿素a、b含量显著增加,叶绿素a/b值无显著影响。(2)SO2胁迫显著抑制了两树种的净光合速率(Pn);在SO2胁迫下巨桉气孔导度(Gs)、胞间CO2浓度(Ci)和蒸腾速率(Tr)显著上升,而天竺桂的Gs和Tr显著被SO2抑制,Ci随SO2浓度的增加先升高后降低。(3)巨桉表观量子效率(AQY)、暗呼吸速率(Rd)、光补偿点(LCP)和光饱和点(LSP)及天竺桂Rd和LCP均随着SO2浓度的增加而先升高后降低,而天竺桂的AQY和LSP逐渐降低。(4)一天中,SO2胁迫显著提高了巨桉Pn、Gs和Tr,而对天竺桂Pn无显著影响,较低浓度SO2胁迫显著促进了天竺桂Gs和Tr,高浓度SO2胁迫则显著抑制其Gs和Tr;SO2胁迫显著抑制了两种植物的Ci。(5)SO2胁迫下,巨桉和天竺桂幼树叶片硫含量均显著增加。研究认为,巨桉对较低浓度的SO2胁迫有一定的适应能力,但对高浓度SO2胁迫的抗性不如天竺桂强,这可能与二者不同的叶片形态及生理特性有关。     

Convergent pathways of gibberellin A1 biosynthesis in Brassica

[²H, ³H]Gibberellin A₄ (GA₄) or [²H, ³H] GA₉ were applied to the shoot tips of seedlings of elongated internode (ein), a tall mutant of rapid cycling Brassica rapa. Following [²H]GA₉ application, [²H]GA₅₁, [²H]GA₂₀ and [²H]GA₄ were identified as products by GC-MS, while [²H]GA₃₄ and [²H]GA₁ were formed from [²H]GA₄. Other isotopically labelled products, including abundant putative conjugates, were also produced, but were not identified. Thus, in B. rapa, GA₁ biosynthesis involves the convergence of at least two metabolic pathways; it can be formed via GA₄ or GA₂₀, the latter of which can originate from GA₉ or from GA₁₉.     

不同培养条件对勺叶茅膏菜试管苗矶松素含量的影响

为探讨培养条件对勺叶茅膏菜(Drosera spatulata)试管苗矶松素积累的影响,采用高效液相色谱(HPLC)法测定矶松素含量,对不同器官和不同培养条件下的勺叶茅膏菜试管苗矶松素含量变化进行研究。结果表明,勺叶茅膏菜试管苗根的矶松素含量显著高于叶片;光质和有机物含量对勺叶茅膏菜试管苗矶松素含量的影响不显著,但对试管苗的生长具有显著影响,最佳培养光质为白光,其次为红光和蓝光,最后为绿光;适当降低培养基中有机物含量可促进勺叶茅膏菜试管苗的生长发育;植物生长调节剂对矶松素积累的影响效应依次为6-BANAAKTGA3,而对试管苗生长的影响效应依次为6-BAGA3NAAKT。因此,勺叶茅膏菜试管苗的最佳培养条件为:以1/2MS为基本培养基,添加0~0.2 mg L–1 6-BA、0.2 mg L–1 NAA、0.5 mg L–1KT和0.1 mg L–1 GA3,于白光下培养。     

Factors influencing the growth of micropropagated shoots and in vitro flowering of gentian

About 70% of the shoots developed from nodal explants ofGentiana triflora flowered in vitroondouble strength WPM medium containing 3% (w/v) sucrose, 0.5mg/l BA after 12 weeks of culture in a growth room at 22°Cwith continuous illumination (PPFD=60molm^–2 s^–1). The influences oninvitro shoot development and flowering of several factors includingthe position of the explant, requirements for sucrose, cytokinin orGA₃, variations of pH and photosynthetic photon flux density (PPFD)were investigated. In vitro flowering but not shootdevelopment of G. triflora decreased notably withincreaseddistance from the apex of the shoot, indicating the presence of a floralgradient in the micropropagated shoots. Conversely, as little as 0.01mg l^–1 GA₃ in the medium promotedshootdevelopment but even up to 0.2 mg l^–1GA₃ did not induce in vitro flowering.Even though BA could substitute GA₃ for a high level of shootdevelopment, it also promoted a high level of in vitroflowering at the PPFD of 60 molm^–2 s^–1. Sucrose was required for shootdevelopment and flowering in vitro and higher levels ofPPFD could not compensate effectively for the omission of the sugar from themedium. In general, the effects of different concentrations of BA in the mediumor variations of pH on shoot development and flowering invitro were found to be influenced by PPFD. A novel observation isthat precocious flowering of micropropagated gentian shoots did not occur ifthey were first cultured for 5 weeks in the dark before transfer to the lightcondition.     

The identification and metabolism of GA9 and its metabolites in seed coats and shoots of pea,line G2

[³H]gibberellin A₉ was applied to shoots or seed parts of G2 pea to produce radiolabeled metabolites. These were used as markers during purification for the recovery of endogenous GA₉ and its naturally occurring metabolites. GA₉ and its metabolites were purified by HPLC, derivatized and examined by GC-MS. Endogenous GA₉, GA₂₀, GA₂₉ and GA₅₁ were identified in pea shoots and seed coats. GA₅₁-catabolite and GA₂₉-catabolite were also detected in seed coats. GA₇₀ was detected in seed coats following the application of 1 g of GA₉. Applied [³H]GA₉ was metabolized through both the 13-hydroxylation and 2-hydroxylation pathways. Labeled metabolites were tentatively identified on the basis of co-chromatography on HPLC with endogenous compounds identified by GC-MS. In shoots [³H]GA₅₁ and [³H]GA₅₁-catabolite were the predominant metabolites after 6 hrs, but by 24 hrs there was little of these metabolites remaining, while [³H]GA₂₉-catabolite and an unidentified metabolite predominated. In seed coats [³H]GA₅₁ was the initial product, later followed by [³H]GA₅₁-catabolite and an unidentified metabolite (different from that in shoots), with lesser amounts of [³H]GA₂₀, [³H]GA₂₉ and [³H]GA₂₉-catabolite. [³H]GA₇₀ was a very minor product in both cases. [³H]GA₉ was not metabolized by pea cotyledons.Edited by T.J. Gianfagna.Author for correspondence