吲哚乙酸在植物细胞中的代谢及其作用

IAA在植物体内参加了细胞伸长生长、形成层细胞分裂、维管组织分化、叶片和花的脱落等许多生理生化过程的调节与控制,对植物的顶端优势、向性、同化物的运输等也有调节作用。植物体通过IAA的生理作用依赖于IAA在细胞内的合成、代谢并通过不同的信号传导途径引起不同效应。     

3-吲哚乙酸对铜钱草去除氮磷的影响

迅猛发展的水产养殖业在带动经济发展的同时,也引发了一定的环境问题,如养殖废水任意排放,引起河流、湖泊、水库等水体富营养化。水生植物可通过植物根系的吸附、转化、富集等作用降低水中氮磷的浓度。目前已有一些利用铜钱草吸收氮磷营养盐进而改良水质的研究,但主要集中在对不同水质的氮磷吸收率方面。基于此,文章将研究铜钱草在不同浓度吲哚乙酸的作用下对氮、磷的去除效率和蛋白质生理指标的变化,以期为铜钱草作为废水处理植物的应用提供参考。     

贵州梵净山大型真菌生态分布及其资源评价

本文报道了梵净山的大型真菌365种,分属于124属、41科。其中食用菌105种,药用菌87种,毒菌33种,木腐菌131种及菌根菌114种。梵净山的大型真菌分属于下列林型和植被型:阔叶林型;针阔混交林型;针叶林型;灌丛型和荒地型。营养方式主要分为寄生、腐生和共生三大类群。     

在吲哚乙酸不同位点偶联载体蛋白对其抗体特异性的影响

分别选择吲哚乙醇分子上的Ｃ１位羧基和吲哚环上的Ｎ位作为偶联载体蛋白的位点,用混合酸酐法和甲醛搭桥法分别合成了两种免疫原ＩＡＡ—ＣＯ—ＮＨ一ＨＳＡ和ＩＡＡ－Ｎ－ＢＳＡ,并进而制得了对吲哚乙酸侧链识别能力不同的两种多克隆抗体,分别可特异识别甲酯化ＩＡＡ和游离态ＩＡＡ;用碳化二亚胺法和甲醛搭桥法分别合成ＩＡＡ—ＣＯ—ＮＨ－ＢＳＡｂＩＡＡ—Ｎ—ＯＶＡ两种复合物,以之为包被物,建立了两种ＩＡＡＥＬＩＳＡ。其灵敏度分别为０．３５ｐｍｏｌ和１．８０ｐｐｍｏｌ;检测范围分别为０．７８～８００ｐｍｏｌ和１．９５～２０００ｐｍｏｌ;批内变异系数分别为４．４５％和４．７９％;批间变异系数分别为１．１５％和１．５０％。笔者用这两种ＥＬＩＳＡ检测了兰花气生根和桑树苗样品中ＩＡＡ的含量,发现两种检测结果相当一致。     

金强河高寒地区大型真菌的分布特征

报道了金强河地区的大型真菌52种,分属于18科,32属。其中食用菌29种,药用菌20种,毒菌14种。该区大型真菌的分布与地形密切相关,有3种生态类型:河漫滩的大型真菌、阶地的大型真菌、亚高山坡地的大型真菌,其中阶地的大型真菌在种类和数量上都比其他两种生态类型丰富。     

拟南芥色氨酸与吲哚乙酸生物合成的研究进展

拟南芥色氨酸生物合成途径的研究已逐渐成为植物分子生物学家了解植物基因结构和表达调控最主要的模式系统之一。到目前为止,编码拟南芥色氨酸合成途径的七种酶蛋白的基因已经全部被克隆,并进行了不同程度的分子生物学研究。长期以来,色氨酸一直被认为是植物生长素吲哚乙酸（ＩＡＡ）生物合成（从头合成）的前体物,但近年来人们发现生长素合成的非色氨酸途径可能是其在植物中生物合成的主要途径。植物在不同的发育阶段可能采用不同的方式合成ＩＡＡ。     

广西花坪国家级自然保护区大型真菌资源及生态分布

报道了广西国家级花坪自然保护区的大型真菌201种,隶属105属45科;其中食用菌50种,药用菌38种,毒菌13种,菌根菌59种和木腐菌48种.保护区的大型真菌按植被类型分为5种群落类型:常绿阔叶林型、亚热带落叶阔叶林型、亚热带中山落叶常绿阔叶混交林型、灌丛型和竹林型;按垂直分布带分为3种林带型:低山林带型、中山林带型和山顶林带型.     

庐山大型真菌的生态分布

报道了庐山的大型真菌２０２种,分属于８１属,属４１科,其中食用菌１０４种,药用菌７１种,毒菌２６种,菌根菌３３训及木腐菌８９种。庐山的大型真菌分属于下列植类型中、阔叶林型、针阔混交林型、针叶林型、竹林、灌丛型和茺地型。并对庐山的大型真菌生趣分布进行了初步分析。     

赤霉酸和吲哚乙酸对器官脱落和离区纤维素酶的影响

赤霉酸(GA_3)处理菜豆叶柄和棉苗子叶柄外植体,离区的纤维素酶活力增加,而吲哚乙酸(IAA)则抑制离区纤维索酶的活力。这与GA_3促进菜豆叶柄和棉苗子叶柄外植体的脱落、IAA延迟脱落的效应成正相关。GA_3促进菜豆叶柄外植体的脱落可被环己酰亚胺(CHI)所阻止,而且离区纤维素酶的活力也显著降低。但在棉铃柄离区并没有观察到GA_3与脱落和离区纤维素酶活力三者之间的相关性。GA_3对棉株上未受精棉铃具有明显的防脱效果,而对棉铃柄外植体有促进脱落的作用,但二者离区纤维素酶活力无明显的差异。     

毛乌素沙地克隆植物沙鞭生长对AM真菌生态分布的影响

从毛乌素沙地沙鞭群落间隔空地沙鞭根状茎延伸方向设置样地,2007年5月、7月和10月在0-10、10-20、20-30、30-40和40-50 cm共5个土层分别采集土壤样品,研究了AM真菌时空分布及沙鞭侵入间隔空地前后对AM真菌分布的影响。结果表明,沙鞭能与AM真菌形成良好共生关系,菌根结构为中间型(I-型),AM真菌定殖率和孢子密度有明显的时空分布规律,并与土壤因子密切相关。随采样时间后延AM真菌定殖率先增后降,最大值出现在7月份;孢子密度先降后增,最大值出现在10月份。土壤采样深度对AM真菌定殖和孢子密度有显著影响,AM真菌最高定殖率和最大孢子密度均出现在0-20 cm浅土层。孢子密度仅与泡囊定殖率显著正相关。土壤速效N与菌丝和总定殖率极显著负相关;土壤温度与泡囊、丛枝、菌丝和总定殖率显著和极显著正相关,与孢子密度显著负相关;土壤湿度与丛枝、菌丝和总定殖率显著正相关,与孢子密度显著负相关。克隆植物沙鞭的生长对土壤AM真菌活动和分布有很大影响,沙鞭入侵前后样地中AM真菌孢子密度和定殖率变化显著。     

Catabolism of indole-3-acetic acid in citrus leaves: identification and characterization of indole-3-aldehyde oxidase

A new enzyme, named indole-3-aldehyde oxidase (IAldO), was identified in citrus ( Citrus sinensis L. Osbeck cv. Shamouti) leaves. The enzyme was partially purified by (NH₄)₂SO₄ fractionation. Sephadex G-200 gel filtration and DEAE-cellulose ion exchange chromatography. IAldO catalyzes the oxidation of indole-3-aldehyde (IAld) to indole-3-carboxylic acid (ICA) with the production of H₂O₂. The enzyme is highly specific for IAld. The apparent K_M of the enzyme for IAld is 19 μ M . The optimum oxidation of IAld occurs at pH 7. 5. The molecular mass of the enzyme, as determined by Sepharose-6B gel filtration, is about 200 kDa. Based on inhibitor studies, it is concluded that IAldO is not a flavin-linked oxidase and there is no requirement for free sulfhydryl groups or divalent cations for maximum activity. The enzyme is strongly inhibited by benzaldehyde. Ethylene pretreatment, wounding and aging of leaf tissues did not affect enzyme activity, suggesting that the enzyme is constitutive in citrus tissues.     

Mode of action of glyphosate in relation to metabolism of indole-3-acetic acid

Studies were conducted with radio-labeled indole-3-acetic acid ([2-¹⁴C] IAA) and tobacco callus culture ( Nicotiana tabacum L. cv. White Gold) to investigate the mode of action of the herbicide glyphosate (N-phosphonomethylglycine). The tissue was first grown with or without glyphosate for 1 to 14 days and then incubated with [2-¹⁴C] IAA for 4 h. Metabolism of [2-¹⁴C] IAA in the tissue was studies by solvent fractionation, high performance liquid chromatography and liquid scintillation counting. The tissue grown with 0.2 m M glyphosate had low level of free [2-¹⁴C] IAA and high levels of other fractions containing metabolites and conjugates of the labeled IAA. After 1 day of glyphosate treatment the free [2-¹⁴C] IAA level in the tissue was reduced by 77% compared to that of the control; after 10 days of treatment the decrease was 96%. The decrease in the free [2-¹⁴C] IAA level was not due to inhibition of IAA uptake, but due to enhanced rates of oxidation and conjugate formation of IAA. The increased oxidation of IAA in the treated tissue was not due to a direct effect of glyphosate on IAA-oxidase since glyphosate was inactive on IAA oxidation in a cell-free system in vitro. The glyphosate-induced growth inhibition was partially overcome by addition of 1 μ M 2,4-dichlorophenoxyacetic acid to the medium. The results lead to the conclusion that glyphosate inhibits growth by depletion of free IAA through rapid acceleration of both conjugate formation and oxidative degradation of IAA.     

Effects of phenolic substances on metabolism of exogenous indole-3-acetic acid in maize stems

Four-day-old stem segments of Zea mays L. cv. Seneca 60 were treated sequentially with phenolic substances and indole-3-acetic [2-¹⁴C] acid ([2-¹⁴C]IAA). Formation of bound IAA was rapid, but a pretreatment with p-coumaric acid, ferulic acid or 4-methylumbelliferone decreased the level of bound IAA. The decrease is not likely related to the effect of the phenolics on enzymic oxidation of IAA, since the level of free IAA was not limiting and the activity of ferulic acid in enzymic oxidation of IAA is different from that of p-coumaric acid and 4-methylum-belliferone. Apparently these compounds inhibited the formation of bound IAA and consequently caused an accumulation of free IAA. In contrast, caffeic acid, protocatechuic acid and 2,3-dihydro-2, 2-dimethyl-7-benzofuranol had little effect. After the uptake of IAA there was a slow but steady incorporation of the radioactivity into the 80% ethanol-insoluble, 1 M NaOH-soluble fraction. Phenolic substances also affected this process. The compounds which are cofactors of IAA-oxidase increased the incorporation while those which are inhibitors of IAA-oxidase decreased the incorporation. Results suggest that the phenolics also affected the enzymic oxidation of IAA in vivo in the same way as in vitro.     

Immunohistochemical observation of indole-3-acetic acid at the IAA synthetic maize coleoptile tips

To investigate the distribution of IAA (indole-3-acetic acid) and the IAA synthetic cells in maize coleoptiles, we established immunohistochemistry of IAA using an anti-IAA-C-monoclonal antibody. We first confirmed the specificity of the antibody by comparing the amounts of endogenous free and conjugated IAA to the IAA signal obtained from the IAA antibody. Depletion of endogenous IAA showed a corresponding decrease in immuno-signal intensity and negligible cross-reactivity against IAA-related compounds, including tryptophan, indole-3-acetamide, and conjugated-IAA was observed. Immunolocalization showed that the IAA signal was intense in the approximately 1 mm region and the outer epidermis at the approximately 0.5 mm region from the top of coleoptiles treated with 1-N-naphthylphthalamic acid. By contrast, the IAA immuno-signal in the outer epidermis almost disappeared after 5-methyl-tryptophan treatment. Immunogold labeling of IAA with an anti-IAA-N-polyclonal antibody in the outer-epidermal cells showed cytoplasmic localization of free-IAA, but none in cell walls or vacuoles. These findings indicated that IAA is synthesized in the 0–2.0 mm region of maize coleoptile tips from Trp, in which the outer-epidermal cells of the 0.5 mm tip are the most active IAA synthetic cells.     

Aromatic amino acid aminotransferase activity and indole-3-acetic acid production by associative nitrogen-fixing bacteria

In this work, we report the detection of aromatic amino acid aminotransferase (AAT) activity from cell-free crude extracts of nine strains of N(2)-fixing bacteria from three genera. Using tyrosine as substrate, AAT activity ranged in specific activity from 0.084 to 0.404 micromol min(-1)mg(-1). When analyzed under non-denaturating PAGE conditions; and using tryptophan, phenylalanine, tyrosine, and histidine as substrates Pseudomonas stutzeri A15 showed three isoforms with molecular mass of 46, 68 and 86 kDa, respectively; Azospirillum strains displayed two isoforms which molecular mass ranged from 44 to 66 kDa and Gluconacetobacter strains revealed one enzyme, which molecular mass was estimated to be much more higher than those of Azospirillum and P. stutzeri strains. After SDS-PAGE, some AAT activity was lost, indicating a differential stability of proteins. All the strains tested produced IAA, especially with tryptophan as precursor. Azospirillum strains produced the highest concentrations of IAA (16.5-38 microg IAA/mg protein), whereas Gluconacetobacter and P. stutzeri strains produced lower concentrations of IAA ranging from 1 to 2.9 microg/mg protein in culture medium supplemented with tryptophan. The IAA production may enable bacteria promote a growth-promoting effect in plants, in addition to their nitrogen fixing ability.     

Identification of enzymes involved in indole-3-acetic acid degradation

Strains of Bradyrhizobium japonicum with the ability to catabolize indole-3-acetic acid (IAA) and strains of B. japonicum, Rhizobium loti, and Rhizobium galegae, unable to catabolize IAA, were analyzed for enzymes involved in the pathway for IAA degradation. Two enzymes having isatin as substrate were detected. An isatin amidohydrolase catalyzing the hydrolysis of isatin into isatinic acid was found in some B. japonicum strains and in two Rhizobium species, R loti and R. galegae. The enzyme was inducible (4–5-fold) by its substrate, isatin, and the partially purified enzyme from R. loti showed an apparent K_M of 11 M for isatin. A NADPH-dependent isatin reductase was measured in extracts from a strain of B. japonicum lacking the isatin amidohydrolase. The structure of the reaction product, dioxindole was verified by NMR spectroscopy. Isatin reductase activity was also detected in extracts of dry pea seeds, and present in at least two isoforms. A low K_M of 10 M for isatin was found with a partially purified preparation of the pea enzyme. The presence of such an enzyme activity in pea indicates dioxindole and isatin as possible intermediates in IAA degradation in pea.     

Glyphosate-increased levels of indole-3-acetic acid in yellow nutsedge leaves correlate with gentisic acid levels

The effects of glyphosate [N-(phosphonomethyl)glycine] on endogenous in-dole-3-acetic acid (IAA) level, IAA oxidase activity, and possible interactions with alterations in phenolic metabolism have been examined in yellow nutsedge ( Cyperus esculentus L.) plants. IAA was quantified by flame ionization detector gas-chroma-tography, phenols were quantified by high-performance liquid chromatography and the auxin protection and the IAA oxidase activities were determined spectrophoto-metrically and/or polarographically. A significant increase in IAA content was recorded after glyphosate treatment. No IAA oxidase activity was detected in control and treated tissues. Auxin protection activity and gentisic acid were present in all extracts assayed, and their concentrations increased as the rate of glyphosate application increased. Addition of gentisic acid to an extract of control plants increased the auxin protection detected. These findings indicate that the high levels of free IAA in yellow nutsedge leaves after glyphosate application are due to the inhibition of the IAA oxidase activity by increased levels of the IAA-protecting phenol gentisic acid.     

Free radical and free radical scavenger effects on indole-3-acetic acid levels and ethylene production

Stable free radicals, together with horseradish peroxidase, promoted degradation of indole-3-acetic acid (IAA). These reactions were retarded by the free radical scavengers Bromoxynil, Na-benzoate and kinetin. Certain free radicals promoted, but the free radical scavenger Bromoxynil retarded ethylene production in apple slices and mung bean stem tissues. The interdependency of free radicals and free radical scavengers in systems controlling IAA levels and ethylene production is discussed.     

Promotion of hypocotyl elongation in loblolly pine (Pinus taeda L.) by indole-3-acetic acid

Elongation of excised loblolly pine ( Pinus taeda L.) hypocotyls was promoted by indole-3-acetic acid and the fungal metabolite, fusicoccin. Gibberellic acid, kinetin, zeatin, or zeatin-riboside were either without effect or promoted elongation only slightly. The most auxin-responsive tissue was just below the cotyledonary node, and elongation was confined to sections excised from the upper 2 cm of the hypocotyl. Indole-3-acetic acid induced elongation rates in the hypocotyl sections equal to those of intact hypocotyls when the sections were excised from young seedlings. Elongation rates decreased in intact hypocotyls before the excised tissues lost responsiveness to the auxin. Hypocotyl elongation in loblolly pine is discussed in relation to hypocotyl elongation in angiosperm species.     

Immunocytochemical localization of indole-3-acetic acid in primary roots of Zea mays

Colloidal gold-labelled antibody was used to localize indole-3-acetic acid in caps of primary roots of Z. mays cv. Kys. Gold particles accumulated on the nucleus, vacuoles, mitochondria, and some dictyosomes and dictyosome-derived vesicles. This is the first localization of indole-3-acetic acid in dictyosomes and dictyosome-derived vesicles and indicates that dictyosomes and vesicles constitute a pathway for indole-3-acetic acid movement in and secretion from root cap cells. Our findings provide cytochemical evidence to support the hypothesis that indole-3-acetic acid plays an important role in root gravitropism.