GA_3,BA和NAA对马铃薯试管薯形成的效应(简报)

正交试验结果表明,马铃薯在离体条件下培养基中添加BA 或NAA有试管薯产生;添加GA_3试管薯不形成。块茎形成以培养基中含 BA5mg/L;BA2mg/L NAA2mg/L和BAlmg/L NAA5mg/L较好。三种植物生长调节物质对试管薯重量的影响大小顺序为NAA>GA_3>BA。     

BA对花生叶片腺苷酸含量和能荷的影响

去顶去根花生幼苗库叶（上位叶）经１０＾－５ｍｏｌ／Ｌ ＢＡ涂抹处理１２ｈ和４８ｈ时,库叶ＡＴＰ含量增加,分别高于对照１９．４％和３３．１％。ＡＤＰ含量在处理后１２－３６ｈ,不断增加,以后逐渐降低,接近对照水平,ＢＡ处理库叶减少ＡＭＰ含理。ＢＡ促进库叶能荷值增加,调节总腺苷酸含量的动态变化。ＢＡ处理库叶１２ｈ,叶片组织和线粒体呼吸速率增加,加强了线粒体氧化磷酸化和能量传递的过程。     

BA对花生叶片蔗糖和淀粉代谢有关酶活性的影响

用１０－５ｍｏｌ／ＬＢＡ处理去顶去根花生幼苗库叶２４ｈ内．蔗糖磷酸合成酶和细胞质果糖－１,６－二磷酸酯酶活性逐渐增加．酸性转化酶活性降低．使蔗糖含量提高,α－淀粉酶活性的增强,促进淀粉分解。ＢＡ处理２４ｈ后,随着蔗糖磷酸合成酶和细胞质果糖－１．６－二磷酸酯酶活性的减弱．酸性转化酶活性逐渐增加．蔗糖含量减少,有利光合碳在淀粉的积累．     

青霉素和NAA与6—BA配合在离体草莓器官建成中的作用

本实验研究了青霉素和ＮＡＡ与６－ＢＡ配合对离体草莓器官建成以及体内过氧化物同工酶的影响。结果表明：青霉素促进不定根的分化,但抑制不定根的伸长和不定芽的分化,并且不同程度地影响器官建成过程中过氧化和抽工酶的谱带和活性。青霉素与植物激素一样,参与了植物体内的生理代谢而引起植物器官建成。     

花生结荚期间生长素,赤霉素和乙烯的变化

在花生子房入地前的1～2天,生长素含量和乙烯释放量均较低,而赤霉素含量较高;入地后,子房膨大前1～3天,生长素含量和乙烯释放量均迅速增加,分别是入地前的10倍和3倍,赤霉素含量则迅速下降,仅为入地前的六分之一。子房膨大开始后,这三种激素均有较高的水平。在子叶分化期后,三种激素含量开始逐渐下降。     

不同激素对花生离体分化的影响

对TDZ和2,4-D等激素在花生成熟胚外植体分化中的影响进行了研究.结果表明,花生成熟胚3～5 d龄实生苗的幼叶和胚轴在低浓度TDZ的诱导下,可分化产生高频不定芽和少量体细胞胚,转到无激素MS培养基或MS BA 0.5 mg/L NAA 0.4 mg/L的培养基后形成丛生苗.丛生苗分离后转入含1/2 MS(大量元素) IBA 0.4 mg/L的培养基中诱导生根,可形成完整的再生植株.幼叶分化率高于胚轴,但胚轴分化成苗速度快.无菌水浸泡16～24 h的胚轴在5～ 30 mg/L 2,4-D的诱导下,分化产生低频不定芽;而胚叶则产生高频体细胞胚,但畸形较严重.     

Dual effect of light on flowering and sprouting of rose shoots

Shade, caused by a dense leaf canopy in the light conditions of a normal greenhouse, reduced sprouting of the third axillary bud (from the top) on decapitated rose branches ( Rosa hybrida cv. Marimba) in comparison to less shaded buds on branches protruding above the canopy and sparsely spaced. Flowering of the third young shoot on shaded branches bearing 3 lateral shoots was totally inhibited. Mixed fluorescent and incandescent light in a growth chamber reduced sprouting of the third bud on decapitated rose branches in comparison to decapitated branches on rose plants held in fluorescent light of similar photon flux density. This was attributed to the higher R:FR ratio in fluorescent vs mixed light that reached the third bud, and in exposed vs shaded branches. Flowering of the third shoot was promoted by several factors: high photon flux density, 0.5 m M gibberellic acid (GA) or 0.2 m M benzyladenine (BA). BA was the most effective treatment. Treatments promoting flowering of the third shoot did not reduce growth or flowering of the upper shoots. However, spraying the uppermost shoot with BA suppressed the growth of the shoots below. It is concluded that light affects flowering in two ways. The effect on bud sprouting is related mainly to R:FR ratios, while the effect on flower development is related mainly to photon flux density. Cytokinins may substitute for the light effect on flower development.     

The Influence of NAA, BA and Temperature on Shoot and Root Development from Begonia×cheimantha Petiole Segments Grown in vitro

The effect of exogenously supplied NAA and BA on the shoot and root formation in isolated petiole segments of Begonia×cheimantha was determined in vitro on a modified White medium at a constant temperature of 24°C. The best development of normally appearing plants was obtained on media containing 0.01 mg × 1^?1 of NAA and 0.5 to 1.0 mg × 1^?1 of BA. Lower concentrations of BA yielded no shoots, higher concentrations promoted shoot formation, but the shoots were abnormal with malformed leaves. Lower concentrations of NAA resulted in poorer survival rate and no roots, with higher concentrations of NAA many roots developed, but these were thickened and their longitudinal growth inhibited. Temperature proved to be of utmost importance for the induction of shoot formation. Thus significantly fewer shoots were formed at the higher temperature (25°C) than at lower temperatures (15 to 20°C). Temperature immediately after initial transfer was of greatest importance: 25°C, during the first week followed by low temperature, produced very few shoots.     

Physiological effects of temperature and growth regulators on foliar chlorophyll,soluble protein,and cold hardiness in citrus

Leaf chlorophyll (Chl, A, B) and total soluble protein were assayed in greenhouse-grown 1.5-year-old trees of 2 citrus types, trifoliate orange (Poncirus trifoliata (L.) Raf.) and sour orange (Citrus aurantium L.) exposed to 12 h (day/night) photoperiods in growth chambers under high (30°/21°C, day/night; noncold-hardening) and low (16°/5°C; cold-hardening) temperature regimes. Trees were sprayed 2 × per week for 5 weeks with one of the following solutions at 100 M: napthaleneacetic acid (NAA), paclobutrazol (2RS, 3RS)-1-(4-chlorophenyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol) (PPP333), benzyl-adenine (BA), abscisic acid (ABA), gibberellic acid (GA₃), minerals only (N, P, K, S, Ca, Mg) and BA (+) minerals. NAA, PP333, ABA and GA₃ decreased Chl A, B and soluble protein in both citrus types under cold-hardening conditions in contrast to increases with the use of BA and BA (+) minerals especially in trifoliate orange. Both BA and GA₃ increased Chl A, B and protein synthesis under high temperature in both citrus types. Under noncold-hardening temperatures, GA₃ enhanced Chl A, B but sharply reduced foliar protein concentration. Dieback of both cultivars following exposure to temperatures down to –6.7°C was decreased 7% by NAA sprays during noncold-hardening temperatures. Cold tolerance of noncoldhardened trifoliate orange trees was also improved with ABA and PP333. Foliar sprays of NAA (sour orange) and PP333 and BA (+) minerals (trifoliate) increased cold tolerance of cold-hardened trees by 8%. Results indicate that spray applications of growth regulators influence physiological factors associated with foliar functioning and cold tolerance in citrus during different temperature regimes.Summary Growth promoters (BA) and inhibitors (NAA) have the potential to promote cold hardines through either a strong stimulatory effect on foliar physiology or a marked inhibition of growth in general. This suggests that each growth regulator may possess an independent role in the cold-hardiness phenomenon and may also interact with physiological processes other than soluble protein and chlorophyll metabolism. The relationship between soluble protein levels in citrus foliage and the degree of cold hardiness remains uncertain and is essentially unresolved pending more specific qualitative research.University of Florida Agricultural Experiment Station Series No. 7446.This paper reports the results of research only. Mention of a trademark of a proprietary product does not constitute a recommendation for use by the U.S. Department of Agriculture to the exclusion of other products that may also be suitable.     

The effect of hormones on heterotrophic growth of a blue-greed alga Westiellopsis prolifica

The heterotrophic growth of the blue-green alga Westiellopsis prolifica was enhanced in presence of GA and IAA. The function of the hormones was found to be influenced by the nature of the substrates supplemented in the growth medium.     

ABA抑制花生侧根发生

本实验研究了ABA对花生侧根发生的影响。结果表明：用10umol·L-1 ABA浸泡处理花生种子1h或在含ABA的培养基上培养,均抑制侧根的发生,侧根发生率降低,数目减少,长度降低,发生的时间推迟1-2d;用ABA合成抑制剂25umol·L-1 NAPR浸泡后的种子,无论在1／2MS还是在含NAA培养基上培养,侧根发生率、侧根的数目和长度均增加。用NAA的极性运输抑制剂10umol·L-1 TIBA浸泡处理种子后,再在含ABA培养基上培养,侧根不发生,说明ABA抑制花生侧根的发生与种子内源ABA和IAA的水平相关。     

Control of Negative Gravitropism and Tension Wood Formation by Gibberellic Acid and Indole Acetic Acid in Fraxinus mandshurica Rupr. var. japonica Maxim Seedlings

In the present study, we investigated the role of gibberellic acid (GA3) and indole acetic acid (IAA) in the gravity response of stems and tension wood formation using two-year-old stems of Fraxinus mandshurica Rupr. var.japonica Maxim seedlings. Forty-five seedlings were used and divided into nine groups that included five seedlings in each group. Seedlings were treated with applications of GA3 alone at concentrations of 2.89 × 10-8and 2.89 × 10-7 μmol/L, IAA alone at concentrations of 5.71×10-8 and 5.71 ×10-7 μmol/L, or their combination to the apical bud of the stem using a micropipette. Seedlings were positioned horizontally after the first treatment.The same treatments were repeated six times per week. At the end of the experiment, all seedlings were harvested. Then, stem segments were cut under a light microscope. Application of exogenous GA3 at the higher concentration stimulated the upward bending of stems, whereas exogenous IAA had no effect. A synergistic effect of GA3 and IAA on upward stem bending was observed following application of the two combinations of GA3 and IAA. Moreover, application of exogenous GA3 at the higher dose stimulated wood formation on both the upper and lower sides of the stems, whereas the mixture of GA3 and IAA had a synergistic effect on wood formation in horizontal stems. Application of exogenous IAA alone at the lower concentration (5.71×10-8 μ mol/L) or application of a mixture of the higher concentrations of GA3 (2.89 × 10-7 μmol/L) and IAA (5.71×10-7 μmol/L) inhibited the development of gelatinous fibers (the G-layer) of tension wood on the upper side of the horizontal stems. The differentiation of gelatinous fibers of tension wood was not inhibited by GA3when it was applied alone, whereas the development of the gelatinous fibers of tension wood was strongly affected by the application of IAA. The findings of the present study suggest that the development of the G-layer is not related to the dose of GA3, but needs a relatively lower concentration of IAA.     

High frequency <Emphasis Type="Italic">in vitro</Emphasis> propagation of <Emphasis Type="Italic">Holarrhena antidysenterica</Emphasis> from nodal buds of mature tree

An in vitro method for propagation of Holarrhena antidysenterica Wall. has been developed using nodal explants from mature trees growing in the field. Irrespective of concentrations and combinations of growth regulators used, the axillary and terminal buds sprouted and elongated when inoculated on Murashige and Skoog (MS) medium. The highest numbers of shoots were formed when sprouted shoots were subcultured from MS basal medium onto MS medium containing 2 mg dm⁻³ N⁶-benzyladenine (BA) and 0.5 mg dm⁻³ α-naphthalene acetic acid (NAA). The shoot number further increased upon subculture on MS medium containing 0.5 mg dm⁻³ BA. By repeated sub-culturing of shoots derived from nodal axillary buds, a high frequency multiplication rate was established. The elongated shoots were excised and rooted in auxin free MS basal medium. Ex vitro rooting of in vitro formed shoots was achieved upon dipping the microshoots for 2 min in 2 mg dm⁻³ of indole-3-butyric acid solution. Successful field establishment and high (80–90 %) survival of plants was observed.     

外源GA和ABA对花生籽仁皱缩变异品系荚果生长的影响

以荚果和籽仁生长发育正常的花生品系‘05D610’及其籽仁皱缩变异系‘05D677’为材料,在荚果膨大阶段初期滴加赤霉素(GA,20mg·L~(-1))和脱落酸(ABA,15 mg·L~(-1))处理幼果,检测荚果生长期间幼果或籽仁内源GA、ABA、ZT(玉米素)和IAA(生长素)含量的变化以及荚果和籽仁的生长量特征,以明确激素含量与荚果和籽仁生长发育的关系和‘05D677’籽仁皱缩的原因。结果显示:(1)外源施加GA处理,可显著提高‘05D610’和‘05D677’的内源GA和ZT含量,并推迟内源IAA含量峰值出现的时间,显著提高‘05D610’荚果和籽仁的鲜重、干重,极显著提高了‘05D677’荚果干重。(2)外源施加ABA处理,使‘05D610’内源GA含量显著降低,‘05D677’内源GA和ABA含量显著提高,同时两品系内源IAA含量峰值出现的时间推迟,使‘05D610’和‘05D677’籽仁干重分别显著和极显著提高。研究表明,用适宜浓度外源GA和ABA处理荚果膨大阶段的初期果针,可以调控荚果膨大阶段幼果或者籽仁中内源激素水平,从而提高花生荚果、籽仁产量;荚果膨大阶段内源GA、ABA和ZT含量不足是导致‘05D677’籽仁皱缩的重要原因。     

芥菜(Brassica juncea)花粉胚状体与离体种胚脂肪酸的变化

在油菜改良品质育种中,利用单个花粉胚状体筛选低或无芥酸株系,需要了解花粉胚状体在发育过程中芥酸含量的变化及与其他脂肪酸变化的关系。Gurr(1972),Dasgupta等(1973)和黄尚琼(1980)研究了不同种、不同品种种子发育过程中脂肪酸组成的变化,但均未曾对离体花粉胚状体和离体种胚进行研究。本文在于探索离     

The roles of abscisic acid and ethylene in the abscission and senescence of cocoa flowers

Cocoa flowers have a limited period of longevity; more than 90% of unpollinated flowers abscised within 32 h after anthesis. Abscisic acid (ABA) levels increased significantly prior to abscission. By 21 h after anthesis, ABA levels had increased almost 10-fold, and by 32 h flowers had 20-fold higher levels of ABA than at anthesis. Fluridone completely inhibited both the increase in ABA, the formation of an abscission zone, and the abscission and senescence of flowers. In contrast, ethylene production increased only slightly 21 h after anthesis and was only 2-fold higher after 32 h. Aminoethoxyvinylglycine (AVG) delayed but did not prevent abscission. In cocoa flowers, ABA is the primary regulator of abscission; ethylene accelerates abscission but only in the presence of ABA. Naphthalene acetic acid (NAA) treatment of flowers at anthesis prevented abscission zone formation and flower abscission, but did not induce fruit set. All parts of the NAA-treated flower except the pedicel senesced after 6 days. NAA+AVG treatment only delayed, whereas fluridone treatment completely prevented flower senescence.