若干因子对鸡冠花悬浮培养中花色素苷积累的影响

本文研究几种植物生长调节剂和蔗糖浓度对鸡冠花细胞悬浮培养中花色素苷积累的影响。结果表明,细胞分裂素KT使花色素苷积累明显高于6-BA,且KT在2 μmol/L时积累量最高;2,4-D在2 μmol/L时对花色素苷积累效果明显,其它浓度的2,4-D和NAA对花色素苷积累效果不明显。高浓度蔗糖有利于花色素苷积累;MS+2,4-D(2 μmol/L)+KT(2 μmol/L)+蔗糖(292 mmol/L)为鸡冠花悬浮细胞培养生产花色素苷的最佳培养基。研究中还发现,在黑暗条件培养下无花色素苷积累,推断光是诱导花色素苷积累的主要因素。随着继代次数的增加,花色素苷含量明显增高,但到第4代时基本稳定。     

激素等外源物质对马铃薯愈伤组织花色苷积累的影响

从来源于马铃薯(Solanum tuberosum cv.Chieftain)茎的愈伤组织中分离到白色和红色2种愈伤组织,用鲜重法和分光光度法分别测量愈伤组织的生长量和花色苷的含量,并对激素、抗菌素和糖对马铃薯愈伤组织生长和花色苷积累的影响进行研究。结果表明:低浓度的2,4-D有利于红色愈伤组织的花色苷积累,高浓度的2,4-D促进其生长而不利于花色苷的积累;高浓度的6-BA能促进红色愈伤组织中花色苷的积累并诱导白色愈伤组织花色苷的合成,但抑制其生长;卡那霉素能使白色愈伤组织变红并积累花色苷,高浓度的卡那霉素严重抑制愈伤组织的生长并最终变褐死亡;提高蔗糖浓度能促进愈伤组织花色苷的产生和积累,但超过70g/L时抑制生长。实验结果为今后花色苷生物合成机理研究和花色苷的工厂化生产奠定了基础。     

不同植物生长物质对牛角藓愈伤组织诱导的影响

相同剂量的GA3和2,4-D对牛角藓愈伤组织诱导效果明显,而6-BA、KT和NAA则抑制。光照对愈伤组织的形成有一定的促进作用。     

提取工艺和植物生长调节剂对罗布麻愈伤组织中黄酮含量的影响

以罗布麻愈伤组织粉末为材,在单因素实验的基础上,利用响应曲面法对罗布麻愈伤组织中黄酮的提取工艺进行优化。响应曲面分析结果表明,提取试剂和提取温度对提取的黄酮含量存在显著影响。通过响应曲面分析得到罗布麻愈伤组织中黄酮提取的最佳条件为:提取试剂为70%甲醇,物料比1∶40,提取时间为4 h,提取温度为70℃。培养并比较了30种不同植物生长调节剂浓度与配比诱导100 d生长的愈伤组织中黄酮的含量,结果得出MB+KT(1.0 mg/L)+NAA(0.2 mg/L)上培养约100 d的愈伤组织中黄酮含量最高,为73.90mg/g。测定愈伤组织培养30 d内黄酮的积累动态,探明从培养的愈伤组织提取黄酮的最佳时段。通过优化提取工艺和筛选最佳植物生长调节剂浓度与配比,运用组织培养技术提高了罗布麻愈伤组织中黄酮含量。     

TDZ对喜树愈伤组织生长及色素积累的影响

目的:研究苯基噻二唑基脲(Thidiazuron,TDZ)对喜树愈伤组织生长及叶绿素、花青素积累的影响。方法:采用TDZ单独应用及合并植物激素对喜树愈伤组织进行了继代培养。结果:单独应用TDZ时1mg/L为组织生长最适浓度。1mg/L TDZ+0.5mg/L NAA可显著促进愈伤组织的生长及叶绿素的积累,1mg/L TDZ+0.5mg/L 2,4-D培养条件下花青素含量高于单独应用TDZ培养。结论:TDZ在喜树愈伤组织培养中可替代植物激素并对细胞植物色素积累有明显影响。     

植物生长调节剂的使用和大豆愈伤组织的诱导及保持

以大豆品种“Mapple Arrow”七日龄无菌苗的上胚轴、下胚轴、子叶组织片段和幼嫩茎尖为外植 休,研究了植物生长调节剂的使用和大豆愈伤组织诱导与保持的关系,供从事大豆离体技术的研究者参 考。     

不同碳源对白桦愈伤组织生长和三萜积累的影响

在一个继代周期中,培养基中添加10-50 g.L-1的蔗糖、葡萄糖和果糖后,白桦愈伤组织的鲜重均上升,浓度为20-30 g.L-1的三种糖,其鲜重积累量均较高.培养基中添加不同浓度葡萄糖和果糖的白桦愈伤组织中三萜物质含量先上升后下降,而添加蔗糖的则呈直线上升.其中,葡萄糖,果糖和蔗糖浓度为30 g.L-1的三萜类物质积累量最高.     

不同生长调节剂对马蹄金愈伤组织诱导的影响

马蹄金是一种优良的地被兼观赏草坪植物。采用正交设计试验法 ,研究了四种不同生长调节剂对马蹄金子叶、叶片、叶柄和下胚轴愈伤组织诱导的影响。结果表明 :生长调节剂是诱导愈伤组织的关键 ,2 ,4 D对愈伤组织诱导具有显著的影响 ,适宜于马蹄金愈伤组织诱导的培养基及生长调节剂为MS +1 .0mg/L 2 ,4 D +0 .2mg/L 6 BA +0 .2mg/LKT +1 .0mg/Lα NAA。     

植物生长调节剂对南方红豆杉愈伤组织培养和紫杉醇合成的影响

通过不同种类和水平植物生长调节剂对南方红豆杉(Taxus chinensisvar.mairei)愈伤组织诱导、生长和紫杉醇合成能力影响的研究发现:诱导培养初期,以无植物生长调节剂的MS为基本培养基,在附加不同植物生长调节剂组合作用下愈伤组织产生的时间和生长、在相同植物生长调节剂组合作用下不同外植体愈伤组织的产生时间和生长均表现出较显著差异,2,4-D/NAA高于0.4时,不利于南方红豆杉愈伤组织的诱导。转换到附加不同植物生长调节剂组合的B5培养基上后,随培养继代次数的增加,生长差异逐渐缩小,直至不显著,表明参考不同文献报道最优配方所设计的各植物生长调节剂组合对南方红豆杉愈伤组织的生长均较适宜,有利南方红豆杉愈伤组织生长的植物生长调节剂优化组合没有唯一性。但不同调节剂组合作用下的同源愈伤组织中、相同调节剂作用下不同源愈伤组织中紫杉醇含量均存在着极显著差异,适当水平(2 mg/L)的2,4-D单用,或与适当水平的KT、6-BA、KT GA配合使用,对南方红豆杉愈伤组织紫杉醇的合成较有利,NAA则不太有利,幼茎和叶愈伤组织产紫杉醇的水平较其它愈伤组织为高。     

高压静电场对银杏愈伤组织生长的影响

银杏愈伤组织经１ ．０ｋＶ／ ｃｍ 强度的高压静电处理后, 愈伤组织生长速率提高, 超氧物歧化酶（ＳＯＤ） 活性和蛋白质及糖含量增加,过氧化物酶（ＰＯＤ） 和吲哚乙酸（ＩＡＡ） 氧化酶活性下降。实验表明,正高压静电场促进银杏愈伤组织细胞的生长,与ＨＶＥＦ 影响体内ＳＯＤ、ＰＯＤ 和ＩＡＡ 氧化酶活性以及蛋白质和糖含量的变化相关     

Nicotine Production by Tobacco Callus Tissues and Effect of Plant Growth Regulators

Relationships between callus origin and the nicotine contents as well as conditions of nicotine production in tobacco tissue cultures were investigated. Nicotine contents of callus tissues were remarkably affected by plant growth regulators in the culture medium. Thus, nicotine production was promoted by the regulators at lower concentrations, but gradually inhibited when the concentrations increased over an optimal region which was different among several kinds of the regulators. The nicotine contents also considerably depended on conditions of the callus induction as well as organ from which they were derived, at least just after callus induction. The differences due to the induction conditions were considered to be gradually lost during successive cultures. Thus, the nicotine contents appeared gradually to change to a certain level which mainly depended on the concentration of the regulators added to the culture medium. When such stabilized callus tissues were transferred to a culture medium containing another regulator or different concentration of the regulator, their nicotine contents rapidly changed to a new level depending on the culture conditions during a few successive cultures. The stabilized callus tissues grown on a medium containing 0.1 ppm α-NAA contained 0.5% of nicotine or more, which was almost the same level in root of the intact plant.     

不同植物生长调节物质对细叶小羽藓愈伤组织诱导及分化的影晌

以细叶小羽藓[Haplocladium microphyllum（Hedw．）Broth．】的配子体为外植体,研究了不同植物生长调节物质对细叶小羽藓愈伤组织诱导及分化的影响。结果表明：在Ms培养基中添加不同的植物生长调节物质对细叶小羽藓配子体增殖影响差异很大,具体表现为2,4一D、KT、IBA和IAA促进细叶小羽藓芽体的诱导及生长,NAA抑制细叶小羽藓芽体的诱导,TDZ阿姨、、及6－BA促进细叶小羽藓的配子体产生愈伤组织;在Ms培养基中添加0．3mg·L－1。6-BA最适合愈伤组织的诱导;在MS掊养基中添加1．0mg·L－1。。IBA最适合愈伤组织的分化。     

凤尾鸡冠茎腐病综合防治研究

本文根据凤尾鸡冠茎腐病的发生条件、规律和症状,进行该病的防治研究,得出一套从苗床土壤消毒、苗期和生长期到盛花期的定期预防、控制浇水时间和浇水量、合理施用氮、磷、钾肥等的有效防治措施,使该病发生率从15.4%降至1.3%,并使凤尾鸡冠的综合性状明显改善,有效地提高了产量和质量。     

Plant Growth Regulators in Cucumis melo L. var. flexuosus Naud Fruit during Rapid Growth

The fruit growth of the snake melon (Cucumis melo L. var. flexuosusNaud) and the plant hormones contained in its immature fruitwere investigated. The fruit growth started 5 days after pollinationand its rapid growth continued for about 10 days. During thisperiod the growth rate (length) was 9 cm per day. The finalsize of the fruit was about 120 cm in length and 6 cm in width25 days after pollination. The cell number of the fruit increasedto more than twice that of the fruitlet before pollination.The increase started immediately after pollination and stoppedat 10 days after pollination. On the other hand, no change incell size was observed during the first 7 days after pollination.After this period, rapid growth started and continued to theend of the fruit growth. The cell size increased to more than7 times that of the fruitlet before pollination. In rapidly developing immature fruit including placenta andimmature seeds, trans-zeatin riboside (ZR) and ABA were identifiedwith gas-liquid chromatography-selected ion monitoring or gas-liquidchromatography-mass spectrometry analysis. In addition, thepresence of trans-zeatin (Z) and another very polar cytokinin,and a novel gibberellin-like substance which is probably anisomer of GA₃ was suggested. The possible significance of theseplant hormones in fruit growth is discussed. (Received June 27, 1985; Accepted April 8, 1986)     

Effects of Growth Regulators on the Induction of Anthocyanin Synthesis in Carrot Suspension Cultures

The effects of plant growth regulators were investigated onanthocyanin synthesis induced by removing auxin from carrotsuspension cultures. Of the auxins tested, 2,4-D showed thestrongest inhibiting effect on anthocyanin synthesis and hadthe strongest promoting effect on undifferentiated growth. When2,4-D was added to anthocyanin synthesizing cells, in whichcell division had ceased, anthocyanin synthesis was repressedimmediately, accumulated anthocyanin disappeared and cell divisionresumed. All cytokinins examined promoted anthocyanin synthesisin the absence of auxin. Both gibberellic acid (GA₃) and abscisicacid inhibited anthocyanin synthesis in media lacking 2,4-D,though GA³ showed no effect on cell division. These effectsof growth regulators on anthocyanin synthesis are similar tothose reported for their effects on embryogenesis [Fujimuraand Komamine (1975) Plant Sci. Lett. 5: 359, (1979) Z. Pflanzenphysiol.95: 13, (1980) Z. PJlanzenphysiol. 99: 1]. The relationshipbetween the induction of anthocyanin synthesis, metabolic differentiation,and embryogenesis are discussed. ¹ Present address: Department of Biology, College of Arts andSciences, The University of Tokyo, Komaba, Meguro-ku, Tokyo153, Japan. ² Present address: Biological Institute, Faculty of Science,Tohoku University, Sendai, Miyagi 980, Japan. (Received November 28, 1985; Accepted July 23, 1986)     

Effects of Growth Regulators on Polyamine Content and Peroxidase Activity in Hevea brasiliensis Callus

3, 4-dichlorophenoxyacetic acid (3,4-D) and benzylaminopurine(BAP) at 9 µM (control medium) was compared with 4.5,2.25, and 0.45 µM for ability to induce callogenesis andembryogenesis from seed explants of Hevea brasiliensis. Supplyingthese growth regulators at 4.5 µM for 20 d improved embryogenicpotential compared with the control medium (El Hadrami, Carronand d'Auzac, 1991, Annals of Botany 67, 511–515), sustainedputrescine, spermidine and spermine at a higher level throughoutof much of the culture period (40–70 d), and maintainedlow levels of peroxidase activity. In the control medium, poorcallus embryogenesis is considered a consequence of rapid ageingof tissues characterized by (i) acceleration of an early buttransient production of polyamines, which promoted embryogeniccapacity, and (ii) an early peak in peroxidase activity thatwas positively correlated with callus browning, one of the factorslimiting embryogenesis. Somatic embryogenesis, polyamines, peroxidase, Hevea brasiliensis, rubber-tree     

The Interaction of Plant Growth Regulators and Vernalization on the Growth and Flowering of Cauliflower (Brassica oleracea var. botrytis)

The growth and flowering response of a cold-requiring cauliflower (Brassica oleracea var. botrytis cv. 60 day) to a range of temperatures under 10 h photoperiod and to growth regulator application were investigated. Endogenous gibberellin A₁(GA₁) concentrations were also assessed under these treatments. Flowering and growth of the inflorescence stalk were correlated with plant developmental stage at the time of a vernalizing cold treatment. Temperature and its duration also affected flowering and inflorescence development. The most effective temperature for inflorescence induction was 10 °C. Flowering did not occur in non-vernalized plants (25 °C) even though they had been treated with GA₃. Application of GA₃ promoted inflorescence stalk elongation greatly in vernalized plants (10 °C), but less so in partially vernalized plants (15 °C or 20 °C). Paclobutrazol (PP₃₃₃) sprayed at the 8–9 leaf stage significantly suppressed inflorescence stalk length and slightly delayed flower bud formation and anthesis. Vernalization at 10 °C increased endogenous GA₁ content in both leaves and the inflorescence stalk irrespective of GA₃ or PP₃₃₃ treatment. Application of GA₃ tended to increase GA₁ levels, while PP₃₃₃ significantly reduce GA₁, both irrespective of vernalization. Vernalization is an important factor for flowering, but not curd formation in this cauliflower cv. 60 day and GA₁ is likely a causal factor in inflorescence stalk elongation.