天然抗烟草花叶病毒大分子物质研究进展

天然大分子物质主要包括蛋白、核酸和糖类.本文主要阐述了植物、动物和微生物中天然抗烟草花叶病毒大分子物质的研究与应用现状.关于这些大分子物质的抗病毒机理是多方面的,主要包括抑制病毒的侵染、对植物病毒增殖过程中的干扰和抑制作用、诱导植物的抗病性反应等,并对今后的研究进行了展望.     

用高压液相色谱及气相色谱法测定几种植物的内源激素

吲哚乙酸、赤霉酸、玉米素、玉米素核苷、异戊烯基腺嘌呤、异戊烯基腺嘌呤核苷和脱落酸是重要的天然植物激素,这些物质在植物体内含量很低,但对植物的生长和分化起重要的调节控制作用。为了探讨这些激素的作用机理,这些激素的分析方法一直是植物生理研究中的一个重要课题。植物内源激素的分析,归纳起来有三种方     

芦苇腐解土中酚酸类化感物质的水分响应特性研究

芦苇和虉草均具有较强的去污能力,常作为湿地植物配置于同一人工湿地进行污水处理。芦苇作为一种强化感植物对虉草具有较强的化感作用,在自然湿地和人工湿地中均会出现芦苇代替虉草的现象,且这一现象的发生与土壤含水量存在一定联系,此外,芦苇腐解土对虉草的化感抑制效应与腐解土中总酚酸的量密切相关。为了研究芦苇腐解土中主要酚酸类物质的水分响应特性,筛选出其中对水分响应较为明显的酚酸物质种类,该研究采用高效液相色谱法,通过芦苇枯落物腐解土的制备,对不同水分环境下芦苇腐解土中酚酸类物质进行了分离和鉴定。结果表明:芦苇腐解土中可分离出没食子酸、香豆酸、香草酸、丁香酸、对香豆酸、阿魏酸、水杨酸和苯甲酸等8种酚酸类物质,其中香豆酸、苯甲酸和阿魏酸等3种酚酸类物质含量较高。分离出的8种酚酸类物质的含量与腐解土的相对含水量均呈显著线性负相关关系,即随着腐解土相对含水量的上升,酚酸类物质的含量均呈现下降趋势,且各种酚酸类物质对水分的响应趋势均可用线性方程较好地拟合。其中,香豆酸、没食子酸和阿魏酸对芦苇腐解土的水分响应最为明显。因此,可将香豆酸、没食子酸和阿魏酸作为主要调控目标,通过调控湿地土壤中水分含量,削弱芦苇对虉草的化感抑制效应,从而维持人工湿地中虉草芦苇群落的长期稳定共存。     

甾族糖苷生物碱研究进展

甾族糖苷生物碱是茄科植物中广泛存在的一种物质,存在于植物的叶子、根、花、果实和块茎中,具有多种生物活性,如抗癌、抗真菌、抗病毒、抗氧化及抗炎等功能。关于植物中糖苷生物碱的分布、含量、生物活性及合成代谢途径的研究一直是本领域的研究热点。糖苷生物碱生物合成分子机理的研究将为优良品种的培育提供理论依据。对甾族糖苷生物碱的结构、生物活性及其生物合成途径进行了综述。     

亚临界水萃取植物酚类物质研究进展

亚临界水作为一种无毒、无污染、廉价的溶剂,已应用于天然产物的提取.植物酚类物质是一种特殊的天然产物,其大部分具有很强的抗氧化活性.许多研究结果表明:亚临界水萃取植物酚类物质行之有效.本文概述了亚临界水萃取的原理、影响因素,并总结了国内外利用亚临界水萃取天然酚类物质的发展趋势.     

植物花青素生物代谢调控

花青素是一类重要的天然色素物质,是植物的主要呈色物质之一,近年来花青素在保健方面的作用越来越受到人们的重视,利用基因工程改造植物花青素相关基因,提高花青素含量已成为研究的热点领域。综述花青素的合成途径、调控机理及转基因方面的研究,重点介绍近年来影响花青素合成的分子因素及外部环境因素的研究现状。     

高等植物中异黄酮合成代谢及其调控

异黄酮是植物次级代谢过程中产生的酚类物质,豆科等植物中含量丰富,在动植物体内有着广泛的生理作用。本文综述了高等植物中异黄酮的合成代谢途径及其关键酶以及调控机理。     

半月苔酸与植物生长

不含ABA的植物(如苔纲,Hepaticae)是怎样实现其生长发育的调控的呢?1969年Valia等(Nature,1969,223:1176)从新半月苔(Lunularia cruciata)中分离得到了一类新的天然生长抑制剂——半月苔酸(Iunularic acid),俗称二氢芪羧酸,即2-(4-羟基苯乙基)-6-羟基苯甲酸。藻类植物中也含有这类物质(Ann Rev Plant Physiol,1974,25:259)。它在“激素浓度”下就能抑制苔纲植物叶状体的生长。其含量随日长的变化而变化,但变化趋     

紫茎泽兰根区土壤酚酸类物质组成及其对土传病菌的影响

紫茎泽兰根系释放的化感物质是导致其土壤环境发生变化的重要因素,可为其成功入侵提供有利条件.以空白土样为对照,提取健康和感染棉蚜的紫茎泽兰根区土壤酚酸类化感物质,采用GC-MS分析其组分和相对含量.结果表明：不同处理根区土壤酚酸类化感物质的种类没有变化,但相对含量发生了改变.其中,虫害处理土样中苯甲酸和对羟基苯甲酸的相对含量均显著高于对照,但对羟基肉桂酸的相对含量显著低于对照,且苯甲酸、对羟基苯甲酸和对羟基肉桂酸的相对含量在3种处理土样中的比例存在差异.用上述3种物质单体及它们在3个处理土样的比例复配进行抑菌试验发现：在较低浓度（50～150 mg·L^-1）下,3种化感物质对5种土传性病菌有显著的抑制作用,但复配后对5种病菌的抑制作用各不相同,虫害处理的复配对其中3种病原菌的抑制作用均低于对照和健康植株.     

应用花粉粒鉴定椴树蜜品质的探讨

我国土地辽阔,蜜源植物极为丰富,仅长白山区就有300多种特别是主要蜜源植物椴树的覆盖率较大,蕴藏着大量的蜂蜜资源,被誉为“天然制糖厂”。蜂蜜的种类很多,一般都以蜜源植物名命名,各具独特的色、香、味。以椴树蜜为例,纯正的椴树蜜,为较透明的淡黄色、有浓郁的薄荷香味、甘甜适口,是特种花蜜中     

Benzoic acid metabolism in presence of Schistosoma mansoni infection in mice

The metabolism of benzoic acid was examined in S. mansoni infected CBA mouse. The result showed that control animals dosed with 150 mg/kg benzoic acid resulted in urinary excretion of two metabolites, hippuric acid and benzoic acid glucuronide. Administration of the same dose to animal carrying S. mansoni for a period of over 6 weeks resulted in decreased formation of hippuric acid and total elimination of benzoic acid by glucuronide pathway.     

Metabolism of Benzoic Acid by Bacteria: 3,5- Cyclohexadiene-1,2-Diol-1-Carboxylic Acid Is an Intermediate in the Formation of Catechol

3,5-Cyclohexadiene-1,2-diol-1-carboxylic acid (1,2-dihydro-1,2-dihydroxy-benzoic acid) is converted enzymatically to catechol in cell extracts from Acinetobacter, Alcaligenes, Azotobacter, and three Pseudomonas species. This enzymatic activity is present only in cultures which have been grown in the presence of benzoic acid, and which convert benzoic acid to catechol rather than to protocatechuic acid. The reaction is assayed by the concomitant formation of reduced nicotinamide adenine dinucleotide from nicotinamide adenine dinucleotide. The conversion of [(14)C]benzoic acid to [(14)C]dihydrodihydroxybenzoic acid is demonstrated in cell extracts. A scheme for the conversion of benzoic acid to catechol in bacteria is presented, involving the formation of dihydrodihydroxybenzoic acid from benzoic acid by a dioxygenase which is unstable in cell extracts, followed by the dehydrogenation and decarboxylation of dihydrodihydroxybenzoic acid to catechol by a previously undescribed enzyme. Experiments with anthranilic acid and phthalic acid suggest that dihydrodihydroxybenzoic acid is a metabolite unique to benzoic acid metabolism. Two new methods for assaying benzoic acid dioxygenase are suggested.     

The conversion of L-phenylalanine into benzoic acid on the thylakoid membrane of higher plants.

The conversion of L-phenylalanine into benzoic acid and other aromatic carboxylic acids was investigated in Nasturtium officinale (watercress), Astilbe chinensis, and Hydrangea macrophylla in vivo and in vitro. Comparative feeding experiments with radioactively labelled L-phenylalanine and cinnamic acid administered to intact leaf discs of A. chinensis indicated a rapid formation of benzoic acid from L-phenylalanine, whereas cinnamic acid was a poor precursor. Using a pulse-chase labelling technique followed by a fractionation of the tissue into subcellular components, chloroplasts could be identified as the predominant, if not exclusive, site of benzoic acid formation in A. chinensis. Experiments in vitro with chloroplasts and thylalkoids of N. officinale, H. macrophylla, and A. chinensis demonstrate the capacity of thylakoid membranes to catalyze the degradation of L-phenylalanine to benzoic acid. The results obtained upon stimultaneous incubation with [4'-3H]L-phenylalanine and [3-14C]cinnamic acid lead to the hypothesis that the reaction of L-phenylalanine to benzoic acid proceeds via a cinnamic acid pool which is different from that of soluble cinnamic acid.     

Novel S-adenosyl-L-methionine:salicylic acid carboxyl methyltransferase,an enzyme responsible for biosynthesis of methyl salicylate and methyl benzoate,is not involved in floral scent production in snapdragon flowers

Using a functional genomic approach we have isolated and characterized a cDNA that encodes a salicylic acid carboxyl methyltransferase (SAMT) from Antirrhinum majus. The sequence of the protein encoded by SAMT has higher amino acid identity to Clarkia breweri SAMT than to snapdragon benzoic acid carboxyl methyltransferase (BAMT) (55 and 40% amino acid identity, respectively). Escherichia coli-expressed SAMT protein catalyzes the formation of the volatile ester methyl salicylate from salicylic acid with a K(m) value of 83 microM. It can also methylate benzoic acid to form methyl benzoate, but its K(m) value for benzoic acid is 1.72 mM. Snapdragon flowers do not emit methyl salicylate. The potential involvement of SAMT in production and emission of methyl benzoate in snapdragon flowers was analyzed by RNA gel blot analysis. SAMT mRNA was not detected in floral tissues by RNA blot hybridization, but low levels of SAMT gene expression were detected after real-time RT-PCR in the presence of SAMT-specific primers, indicating that this gene does not contribute significantly, if at all, in methyl benzoate production and emission in snapdragon flowers. Expression of SAMT in petal tissue was found to be induced by salicylic and jasmonic acid treatments.     

Species differences in the metabolism of benzoic acid by isolated hepatocytes and kidney tubule fragments

The metabolism of benzoic acid to hippuric acid and benzoyl glucuronide has been studied in viable hepatocytes and renal tubule fragments from two species of omnivores (rat, hamster) and two species of carnivores (ferret, dog). Hippuric acid formation was detected in hepatocytes and tubules from omnivores but was not detectable in hepatocytes from the two carnivore species. High levels of hippuric acid were produced in the tubules from the carnivores. A small amount of glucuronidation occured in hepatocytes of all these species tested and in the carnivores this reaction was the predominant pathway of benzoic acid metabolism. These results indicated that the marked species differences in patterns of benzoic acid conjugation are related to differences in the ability of liver and kidney cells to carry out glycine and glucuronic acid conjugation.     

Prevention of formation of acid drainage from high-sulfur coal refuse by inhibition of iron- and sulfur-oxidizing microorganisms. II. Inhibition in "run of mine" refuse under simulated field conditions

The combination of sodium lauryl sulfate and benzoic acid effectively inhibits iron- and sulfur-oxidizing bacteria in coal refuse and prevents the conversion of iron pyrite to sulfate, ferric iron, and sulfuric acid, thereby significantly reducing the formation of acidic drainage from coal refuse. The inhibitors were effective in a concentration of 1.1 mg/kg refuse, and data indicate that the SLS was in excess of the concentration required. The treatment was compatible with the use of lime for neutralization of acid present prior to inhibition of its formation.     

Chemical-specific continuous biomonitoring using a recombinant bioluminescent bacterium DNT5 (nagR-nagAa::luxCDABE)

The recombinant bioluminescent bacterium, DNT5, containing a nagR-nagAa::luxCDABE fusion, was tested in a multi-channel continuous monitoring system to evaluate its ability to detect benzoic acid derivatives. Seven chemicals, benzoic acid, salicylic acid, 2,5-dihydroxy benzoic acid, 3,5-dihydroxy benzoic acid, benzene, naphthalene and phenol, were used to characterize the responses of DNT5. This strain responded uniquely to each chemical, and these responses were then evaluated based upon the structures of each chemical. The greatest bioluminescent responses were to salicylic acid and benzoic acid, followed by 2,5-dihydroxy benzoic acid and 3,5-dihydroxy benzoic acid, but DNT5 was unresponsive when exposed to benzene, phenol and naphthalene, suggesting it has a strong preference for benzoic acid derivatives with few or no ring-substituted groups.     

微生物降解苯甲酸的研究进展

苯甲酸在工业中的广泛应用使其成为环境中的常见污染物,对微生物好氧降解苯甲酸的邻位途径、间位途径、龙胆酸途径和原儿茶酸途径及厌氧降解途径等进行总结,并对苯甲酸降解过程中发挥重要作用的苯甲酸双加氧酶的种类、不同组分及苯甲酸降解基因和调控基因的基因簇进行介绍,同时展望微生物降解污染物的发展方向。     

Hydrazide synthesis: novel substrate specificity of amidase

The amidase from Rhodococcus rhodochrous J1, which hydrolyses amide to acid and ammonia, was found to catalyze the synthesis of hydrazide using hydrazine as a substrate. This is the first report on the hydrazide synthesis through enzymatic reactions. The enzyme also acted on benzoic acid in the presence of hydrazine, yielding benzoic hydrazide. Together with the finding that benzoic hydrazide was converted into benzoic acid (when it was used as a substrate in the absence of hydrazine), these unique characteristics suggest that the reaction route for the formation of the acid from the hydrazide and that of the hydrazide from the acid are reversible to each other via the acyl-enzyme. Not only aromatic hydrazides but also aliphatic hydrazides were synthesized from the corresponding amides and hydrazine.     

Pathway of Salicylic Acid Biosynthesis in Healthy and Virus-Inoculated Tobacco

Salicylic acid (SA) is a likely endogenous regulator of localized and systemic disease resistance in plants. During the hypersensitive response of Nicotiana tabacum L. cv Xanthi-nc to tobacco mosaic virus (TMV), SA levels rise dramatically. We studied SA biosynthesis in healthy and TMV-inoculated tobacco by monitoring the levels of SA and its likely precursors in extracts of leaves and cell suspensions. In TMV-inoculated leaves, stimulation of SA accumulation is accompanied by a corresponding increase in the levels of benzoic acid. 14C-Tracer studies with cell suspensions and mock-or TMV-inoculated leaves indicate that the label moves from trans-cinnamic acid to SA via benzoic acid. In healthy and TMV-inoculated tobacco leaves, benzoic acid induced SA accumulation. o-Coumaric acid, which was previously reported as a possible precursor of SA in other species, did not increase SA levels in tobacco. In healthy tobacco tissue, the specific activity of newly formed SA was equal to that of the supplied [14C]benzoic acid, whereas in TMV-inoculated leaves some isotope dilution was observed, presumably because of the increase in the pool of endogenous benzoic acid. We observed accumulation of pathogen-esis-related-1 proteins and increased resistance to TMV in benzoic acid- but not in o-coumaric acid-treated tobacco leaves. This is consistent with benzoic acid being the immediate precursor of SA. We conclude that in healthy and virus-inoculated tobacco, SA is formed from cinnamic acid via benzoic acid.