974 resultados para plant secondary metabolism


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Dengue fever, currently the most important arbovirus, is transmitted by the bite of the Aedes aegypti mosquito. Given the absence of a prophylactic vaccine, the disease can only be controlled by combating the vector insect. However, increasing reports of resistance and environmental damage caused by insecticides have led to the urgent search for new safer alternatives. Twenty - um plant s eed extracts from the Caatinga were prepared , tested and characterized . Sodium phosphate ( 50 mM pH 8.0) was used as extractor. All extracts showed larvicidal and ovipositional deterrence activity . Extracts of D. grandiflora, E. contortisiliquum, A. cearenses , C. ferrea and C. retusa were able to attract females for posture when in low co ncentration . In the attractive concentrations, the CE of E. contortisiliquum and A. cearenses were able to kill 52% and 100% of the larvae respectively . The extracts of A. cearenses , P. viridiflora, E. velutina, M. urundeuva and S. brasiliensis were also pupicides, while extracts of P. viridiflora, E. velutina, E. contortisiliquum , A. cearenses, A. colubrina, D. grandiflora , B. cheilantha , S. spectabilis, C. pyramidalis, M. regnelli e G. americana displayed adulticidal activity. All extracts were toxic to C. dubia zooplankton . The EB of E. velutina and E. contortisiliquum did not affect the viability of fibroblasts . In all extracts were identified at least two potential insecticidal proteins such as enzyme inhibitors, lectins and chitin - binding proteins and components of secondary metabolism . Considering all bioassays , the extracts from A. cearenses, P. viridiflora, E. contortisiliquum , S. brasiliensis, E. velutina and M. urundeuva were considered the most promising . The E. contortisiliquum extracts was the only one who did not show pupicida activity, indicating that its mechanism of action larvicide and adulticidal is related only to the ingesti on of toxic compounds by insect , so it was selected to be fragmenting. As observed for the CE , th e protein fractions of E. contortisiliquum also showed larvicidal activity, highlighting that F2 showed higher larvicidal activity and lower en vironmental toxicity than the CE source. The reduction in the proteolytic activity of larvae fed with crude extra ct and fractions of E. contortisiliquum suggest ed that the trypsin inhibitors ( ITEc) would be resp onsible for larvicidal activity . However the increase in the purification of this inhibitor resulted in loss of larvicidal activity , but the absence of trypsin inhibitor reduced the effectiveness of the fractions , indicating that the ITEC contributes to the larvicidal activity of this extract. Not been observed larvicidal activity and adulticide in rich fraction vicilin, nor evidence of the contribution o f this molecule for the larvicidal activity of the extract. The results show the potential of seeds from plant extracts of Caatinga as a source of active molecules against insects A. aegypti at different stages of its development cycle, since they are comp osed of different active compounds, including protein nature, which act on different mechanisms should result in the death of insec

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Oilseeds are a high-value natural resource, due to its use as a substitute for petroleum. However, the storage time can reduce seed viability and oil quality. Therefore, scientific efforts have been made to provide a increment of storage time, germination rates and plant establishment of high-value oilseeds. The seedling establishment depends of the plant pass over the functional transition stage, characterized by a metabolic change from heterotrophic condition to autotrophic one. The storage oil mobilization is performed by β-oxidation process and the glyoxylate cycle. Also, the functional transition involves acclimation to photosynthetic condition, which generally includes the participation of antioxidant system and the reactive oxygen species, the latter are produced in various reactions of primary and secondary metabolism. In the present study, Catalase was inhibited during the functional transition of sunflower and safflower, after were performed many analyzes to elucidate the effects caused on the SOD and APX antioxidant systems. Also, were checked the changes in expression pattern of the glyoxylate cycle enzymes markers, ICL and MLS. It was observed that after CAT inhibition, the SOD and APX antioxidant systems allow the seedling establishment. Besides, was verified that both oilseeds can be accelerate the reverse mobilization and the photosynthetic establishment when Catalase activity has dramatically decreased

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Tese de Doutoramento, Ciências Agrárias, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2015

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This study reports Agrobacterium rhizogenes-mediated transformation of three cultivars of Ocimum basilicum for hairy root establishment, screening and selection for the production of rosmarinic acid and antioxidants. Hairy root development was found to be explant-specific and virulence-dependent. Distinct inter-cultivar morphological variability was found between the seven axenically developed hairy root lines and morphological traits were found to be correlated with the presence of aux2 genes, their expression and endogenous IAA content. Further inter-cultivar variability in the content of total phenolics, rosmarinic acid and caffeic acid was also found. Production of rosmarinic acid was found to be age-dependent and cultivar-specific. Chemiluminescence analysis showed the hairy roots to be rich in antioxidants and that rosmarinic acid was the major antioxidant molecule. The concentration of rosmarinic acid was found to be positively correlated with the total antioxidant potential of the hairy root extracts. On the basis of origin, morphology and metabolite content, three elite hairy root lines were selected that had significantly higher rosmarinic acid production, biomass and antioxidant potential than non-transformed roots. These new lines are rich reserves of both antioxidants and rosmarinic acid.

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Apples are rich in polyphenols, which provide antioxidant properties, mediation of cellular processes such as inflammation, and modulation of gut microbiota. In this study we compared genetically engineered apples with increased flavonoids [myeloblastis transcription factor 10 (MYB10)] with nontransformed apples from the same genotype, "Royal Gala" (RG), and a control diet with no apple. Compared with the RG diet, the MYB10 diet contained elevated concentrations of the flavonoid subclasses anthocyanins, flavanol monomers (epicatechin) and oligomers (procyanidin B2), and flavonols (quercetin glycosides), but other plant secondary metabolites were largely unaltered. We used these apples to investigate the effects of dietary flavonoids on inflammation and gut microbiota in 2 mouse feeding trials. In trial 1, male mice were fed a control diet or diets supplemented with 20% MYB10 apple flesh and peel (MYB-FP) or RG apple flesh and peel (RG-FP) for 7 d. In trial 2, male mice were fed MYB-FP or RG-FP diets or diets supplemented with 20% MYB10 apple flesh or RG apple flesh for 7 or 21 d. In trial 1, the transcription levels of inflammation-linked genes in mice showed decreases of >2-fold for interleukin-2 receptor (Il2rb), chemokine receptor 2 (Ccr2), chemokine ligand 10 (Cxcl10), and chemokine receptor 10 (Ccr10) at 7 d for the MYB-FP diet compared with the RG-FP diet (P <0.05). In trial 2, the inflammation marker prostaglandin E2 (PGE2) in the plasma of mice fed the MYB-FP diet at 21 d was reduced by 10-fold (P < 0.01) compared with the RG-FP diet. In colonic microbiota, the number of total bacteria for mice fed the MYB-FP diet was 6% higher than for mice fed the control diet at 21 d (P = 0.01). In summary, high-flavonoid apple was associated with decreases in some inflammation markers and changes in gut microbiota when fed to healthy mice.

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Foliar oils, particularly monoterpenes, can influence the susceptibility of plants to herbivory. In plants, including eucalypts, monoterpenes are often associated with plant defence. A recent analysis revealed an increase in foliar oil content with increasing latitudinal endemism, and we tested this pattern using three eucalypt taxa comprising a latitudinal replacement cline. We also examined the relative concentrations of two monoterpenes (alpha-pinene and 1,8-cineole), for which meta-analyses also showed latitudinal variation, using hybrids of these three taxa with Corymbia torelliana. These, and pure C. torelliana, were then assessed in common-garden field plots for the abundance and distribution of herbivory by four distinct herbivore taxa. Differing feeding strategies among these herbivores allowed us to test hypotheses regarding heritability of susceptibility and relationships to alpha-pinene and 1,8-cineole. We found no support for an increase in foliar oil content with increasing latitude, nor did our analysis support predictions for consistent variation in alpha-pinene and 1,8-cineole contents with latitude. However, herbivore species showed differential responses to different taxa and monoterpene contents. For example, eriophyid mites, the most monophagous of our censused herbivores, avoided the pure species, but fed on hybrid taxa, supporting hypotheses on hybrid susceptibility. The most polyphagous herbivore (leaf blister sawfly Phylacteophaga froggatti) showed no evidence of response to plant secondary metabolites, while the distribution and abundance patterns of Paropsis atomaria showed some relationship to monoterpene yields.

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The present study examines patterns of heritability of plant secondary metabolites following hybridisation among three genetically homogeneous taxa of spotted gum (Corymbia henryi (S.T.Blake) K.D.Hill & L.A.S.Johnson, C. citriodora subsp. variegata (F.Muell.) K.D.Hill & L.A.S.Johnson and C. citriodora (Hook.) K.D.Hill & L.A.S.Johnson subsp. citriodora (section Maculatae), and their congener C. torelliana (F.Muell.) K.D.Hill & L.A.S.Johnson (section Torellianae)). Hexane extracts of leaves of all four parent taxa were statistically distinguishable (ANOSIM: global R = 0.976, P = 0.008). Hybridisation patterns varied among the taxa studied, with the hybrid formed with C. citriodora subsp. variegata showing an intermediate extractive profile between its parents, whereas the profiles of the other two hybrids were dominated by that of C. torelliana. These different patterns in plant secondary-metabolite inheritance may have implications for a range of plant-insect interactions.

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Plant secondary chemistry mediates the ability of herbivores to locate, accept and survive on potential host plants. We examined the relationship between attack by the cerambycid beetle Phoracantha solida and the chemistry of the secondary phloem (inner bark) of two differentially attacked plantation forestry taxa, Corymbia variegata and its hybrid with C. torelliana. We hypothesised that this differential rate of attack may have to do with differences in secondary chemistry between the taxa. We found differences in the bark chemistry of the taxa, both with respect to phenolic compounds and terpenoids. We could detect no difference between bored and non-bored C. variegata trees (the less preferred, but co-evolved host). Hybrid trees were not different in levels of total polyphenols, flavanols or terpenes according to attack status, but acetone extracts were significantly different between bored and non-bored trees. We propose that variations in the bark chemistry explain the differential attack rate between C. variegata and the hybrid hosts.

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The regulation of carotenoid biosynthesis in a high-carotenoid-accumulating Fe’i group Musa cultivar, “Asupina”, has been examined and compared to that of a low-carotenoid-accumulating cultivar, “Cavendish”, to understand the molecular basis underlying carotenogenesis during banana fruit development. Comparisons in the accumulation of carotenoid species, expression of isoprenoid genes, and product sequestration are reported. Key differences between the cultivars include greater carotenoid cleavage dioxygenase 4 (CCD4) expression in “Cavendish” and the conversion of amyloplasts to chromoplasts during fruit ripening in “Asupina”. Chromoplast development coincided with a reduction in dry matter content and fruit firmness. Chromoplasts were not observed in “Cavendish” fruits. Such information should provide important insights for future developments in the biofortification and breeding of banana.

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水母雪莲(Saussurea medusa Maxim)为名贵珍稀中药材,其主要药用成分为类黄酮,尤其是3-脱氧类黄酮。目前关于雪莲的研究主要集中在采用细胞培养生产类黄酮等方面,但对于雪莲类黄酮生物合成的分子机制了解甚少,极大限制了这一珍贵资源的利用。本研究采用水母雪莲红色系愈伤组织及悬浮细胞为材料,构建cDNA文库,从中克隆水母雪莲类黄酮次生代谢中的相关基因并对这些基因进行了深入的生物信息学分析、转基因研究初步确定其功能,以期了解雪莲类黄酮次生代谢的分子机制,为提高类黄酮的合成奠定基础。主要结果如下: 1. 成功地构建了水母雪莲红色系愈伤组织与悬浮细胞cDNA文库,原始文库滴度达到4×106pfu/ml,扩增文库滴度接近1011 pfu/ml,重组率达98%。PCR检测插入片段,均在0.5kb到3kb之间,1kb以上占62%。从文库中检测到了chs、dfr及Myb转录因子SmP,文库覆盖度达到要求且为PCR筛选文库提供了可能。 2. 采用部分简并引物,通过RT-PCR克隆了水母雪莲查尔酮异构酶基因Smchi特异探针,并根据这一探针序列设计特异引物,采用TD-PCR法筛选cDNA文库,获得Smchi cDNA序列,全长831bp,编码一个232氨基酸残基的蛋白。根据cDNA序列克隆了Smchi DNA序列,结果表明Smchi基因无内含子。Smchi cDNA序列与翠菊chi基因高度同源,ORF区域同源性高达84%,但推测氨基酸序列则只有79.3%。Smchi mRNA具有复杂的二级结构。SmCHI具有典型的Chalcone结构域,其二级结构与苜蓿CHI蛋白十分相似,7个α-螺旋与8个延伸链由随机结构联系起来。但其活性中心的第三个关键氨基酸残基N115为M115所取代,这一取代可能导致该蛋白无生物活性,也可能使它具有一般CHI不同的功能。构建Smchi正义、反义真核表达载体,通过农杆菌介导导入烟草,获得转正义、反义Smchi基因的烟草。转基因烟草花色未改变,但叶片总黄酮发生了显著的变化,50%转正义基因烟草总黄酮含量显著提高,最高比对照提高6倍,70%转反义基因烟草总黄酮含量显著下降,最多达85.1%,初步证明Smchi具有功能,并能有效调控烟草类黄酮次生代谢。因此,SmCHI可能是不同于已知CHI的一类新的CHI蛋白,它催化的反应可能与花色素合成无关,其反应机制也可能有所不同。 3. 伴随Smchi的克隆获得了一个黄烷酮3-羟化酶类似基因Smf3h的cDNA,全长1334bp,编码一个343aa的蛋白。根据这一cDNA序列克隆了Smf3h DNA序列,全长1630bp,结果表明该基因由4个外显子和3个内含子组成。Smf3h mRNA具有十分复杂的二级结构。 推测蛋白氨基酸同源性分析表明,SmF3H属于2OG-FeII_Oxy家族,与同一家族的的颠茄H6H的同源性为45%,与拟南芥F3H的同源性为40%,但对SmF3H、典型F3H及典型H6H推测蛋白二级结构、活性中心关键氨基酸残基的位置与相对距离、软件进行功能预测分析,发现SmF3H与F3H更相似。构建Smf3h的正义与反义真核表达载体,通过农杆菌介导导入烟草,但只获得一批转正义基因的烟草,反义基因导致烟草不能再生而未获得转反义基因烟草。转基因烟草花色未改变,叶片总黄酮也与对照相似,初步确认Smf3h与烟草类黄酮生物合成无关,而是一个既不属于f3h也不属于h6h的功能未确定的新基因。 4. 采用与克隆Smchi基因相似的方法,从cDNA文库中克隆了SmP基因cDNA,全长969bp,编码一个256 aa的蛋白质。根据cDNA序列克隆了SmP基因的DNA序列,结果表明,SmP基因无内含子。SmP基因cDNA 一级结构及mRNA二级结构预测分析表明,该基因A+T含量很高(63%),所形成二级结构以A-T配对为主,其稳定性可能较差。SmP推测蛋白序列具有R2R3-Myb转录因子的典型特征,在N-端具有两个Myb DNA-binding Domain,其二级结构与鸡Myb转录因子1A5J十分相似,与其他基因如水稻OsMYB、番茄ThMYB的同源区域主要集中在这一结构域,分别为71.3%和70.8%;C-端富含丝氨酸,与烟草NtMYB、葡萄VlMYB等类黄酮调控因子相似,都呈寡聚体分布,并具有相同的保守磷酸化位点S170与S206。构建SmP基因真核表达载体,通过农杆菌介导导入烟草,获得大量转基因烟草。转基因烟草花色未发生改变,但51%的转基因烟草叶片总黄酮含量都显著提高(0.5-6倍),表明SmP具有促进烟草类黄酮生物合成的功能,但所调控的支路与花色素合成无关。初步试验结果表明,转SmP基因烟草对蚜虫具有很高的抗性,可有效地抑制蚜虫在烟草上的生长,抑制率最高可达92%-100%。这一抗性与烟草中类黄酮的积累可能具有直接的联系,但还需要进一步的试验证明。 5. 与美国俄亥俄州立大学Erich Grotewold 博士实验室合作,完成了微型EST库50个克隆的测序并进行了分析,从中获得了水母雪莲花色素合酶基因SmANS及醛脱氢酶基因SmALDH的特异探针。根据SmANS特异探针设计引物,采用PCR从这50个克隆中筛选获得了SmANS的cDNA序列,全长1229bp,编码一个356aa的蛋白质。SmANS在cDNA水平上与同属的翠菊ANS基因高度同源,但同源区域集中在ORF区域,达到80%,mRNA 预测二级结构十分复杂;推测氨基酸序列与翠菊ANS同源性达到82.9%。SmANS属于2OG-FeII_Oxy家族,在2OG-FeII_Oxy结构域高度保守,与翠菊、甜橙ANS保守结构域同源性达到94%。预测蛋白二级结构以α-螺旋-β-折叠为主,由7个主螺旋和11个主β-折叠及随机结构连接而成,并具有2OG-FeII_Oxy家族活性中心的三个保守的组氨酸残基(His84、His235、His291)和一个天冬氨酸残基(Asp237)。 6. 根据微型EST库中获得的SmALDH特异探针设计引物,采用PCR从这50个克隆中筛选获得了SmALDH基因cDNA 序列,全长1664bp,编码一个491aa的蛋白质。SmALDH基因cDNA具有独特的碱基组成,3/-UTR富含A+T,占该区域碱基总量的80%,5/-UTR的A+T和G+C各占50%,比ORF区域(52%)还低,因此其mRNA二级结构中5/-UTR可以单独形成自身二级结构并且十分稳定,这可能影响基因的表达。这一现象在水稻、玉米等植物中也存在。SmALDH在cDNA水平上在ORF区域与拟南芥、藏红花、水稻等具有较高同源性,分别为64.03%、63.89%、63.72%,但在推测蛋白氨基酸序列水平上同源性反而较低,分别为54.9%、54.3%、54.0%。SmALDH缺少线粒体定位信号,为胞质醛脱氢酶,具有一个Aldedh 保守结构域,还具有与1OF7-H相似的以α-螺旋-β-折叠为主的二级结构,由10个主螺旋和15个主β-折叠及随机结构连接而成。由于ALDH在植物细胞乙醇发酵中具有解除醛类物质毒害的功能,因此SmALDH基因的克隆为改造细胞自身以适应发酵培养条件,解决水母雪莲细胞大规模培养中需氧问题提供了可能。

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水母雪莲(Saussurea medusa Maxim)为菊科凤毛菊属植物,是名贵中药材。为解决雪莲资源匮乏,我们实验室通过植物组织培养技术,成功的建立起水母雪莲细胞和毛状根体系。通过对它的药理实验及化学成分分析,主要成分为黄酮类物质和紫丁香甙单体。为了进一步提高这些物质在水母雪莲培养物中的含量,本文开展通过添加外源诱导子手段来调控水母雪莲次生代谢合成途径。 利用水杨酸(SA)和酵母提取物(YE)作为外源诱导子,添加到水母雪莲细胞系和毛状根系培养基中,研究诱导子不同添加浓度和不同添加时间对水母莲细胞系和毛状根系的生长及次生物质合成的诱导效应。实验结果发现:对于细胞系来说,SA比YE的诱导效果要好,低浓度SA处理时,不仅能促进细胞的生长,还能提高水母雪莲细胞中黄酮化合物和紫丁香甙的含量。其中,在细胞生长周期的第6天添加终浓度为20 μM的SA,诱导效果表现最佳。在此条件下,细胞内总黄酮产量达到532 mg/l,紫丁香甙为630 mg/l,分别比对照提高了130%,和150%。对于毛状根体系来说,SA和YE生长早期添加会抑制毛状根生长。总体上,YE的诱导效果比SA明显。在第10天添加终浓度为40 μg/ml的YE,总黄酮达到741 mg/l,紫丁香甙达到303 mg/l,分别是对照的2.8和2.5倍。 同时研究了20 μM和100 μM SA诱导下,黄酮合成途径中相关酶的变化。发现,低浓度的SA能在短时间内诱导CHS和CHI表达,24h后PAL酶活性升高到对照的7.5倍,而48 h总黄酮的含量检测到最高值。因此可以初步断定,SA诱导苯基苯丙烷类物质的积累与CHS和CHI表达,PAL酶活性提高有关。 另外,从水母雪莲cDNA中克隆到雪莲黄酮合成途径的第一个关键酶—查耳酮合成酶基因(SmCHS)全长cDNA。此cDNA序列全长为1313bp,其编码的蛋白为389个氨基酸,推测的氨基酸序列与许多物种都高度同源,同源性高达88%。生物信息学分析,SmCHS具有CHS-like保守结构域,其二级结构与苜蓿的CHS十分相似,且苜蓿中的CHS酶活性中心的关键氨基酸位点在SmCHS也一致对应相同,没有突变。因此可以初步推测这个SmCHS应该具有查耳酮合成酶功能。并进一步构建SmCHS植物表达载体,转化拟南芥chs突变体,通过功能互补分析研究此基因的功能。由于时间关系这部分研究尚在进行中。

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茉莉酸类化合物是一种具有诱导植物次生代谢,抵抗外来侵害,提高植物抗逆防御性等重要作用的植物激素,主要包括茉莉酸(JA)、茉莉酸甲酯(MeJA)及其异亮氨酸衍生物等。茉莉酸的化学合成已报道有十几种之多,但都还无法实现工业化生产,满足农业需求。 本文以α-羧基肉桂酸为起始原料,经过加氢还原、AlCl3-NaCl离子液体中的分子内F-C酰基化反应,HATU催化下与异亮氨酸结合三步反应,合成了一种茉莉酸类似物吲哚异亮氨酸甲酯结合物(Ind-IleMe),总收率约70 %。 用合成的Ind-IleMe、coronalon及MeJA对银杏叶进行诱导,银杏叶经盐酸甲醇溶液加热水解提取黄酮苷元,HPLC检测发现,经诱导后的银杏叶与对照相比银杏黄酮含量均有所增加,最高可诱导银杏叶黄酮含量增长15%—20%,最高诱导浓度coronalon 最低,为1 μmol/L,Ind-IleMe是10 μmol/L,MeJA的诱导浓度最高,大于等于100 μmol/L。 对MeJA诱导后银杏叶的生理生化中几个重要指标进行了测定,发现经诱导后SOD、MDA、PAL、蛋白活性或含量相对升高,叶绿素、可溶性糖含量相对降低,这与MeJA诱导提高银杏叶的逆境防御及次生代谢有关。 在植物的次生代谢中,挥发性气体(VOCs)具有防御草食动物及实现同种及不同种植物间信息交流的重要作用。本文应用自组装的炭阱吸附装置和固相微萃取(SPME)来收集诱导后的银杏叶、利马豆及三种酒中的挥发物,GC-MS检测进行定性定量分析,发现诱导后的银杏叶释放出更多的挥发性有机物,主要是石竹烯等一些参与植物防御机制的倍半萜类,通过对比炭阱吸附和SPME在挥发物的收集上,发现炭阱吸附具有吸附效率更高、样品可短期保存、重复进样分析、可定量等优越性,因此具有很好的发展前景。

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本文采用开顶箱法研究了在连续两年高浓度CO2(700 μmol•mol-1)、O3(80 nmol•mol-1)及其复合作用条件下银杏和油松的生长、初生代谢产物和次生代谢产物含量的季节动态变化、年度动态变化,揭示了银杏、油松次生代谢对高浓度CO2、O3的适应机制及其对树木本身的影响,为研究城市森林对全球变化的响应与反馈提供了重要理论依据。 得出的主要结果如下: 1. CO2倍增处理在2006、2007两个生长季中都增加了银杏、油松叶片中淀粉、可溶性糖、可溶性蛋白的含量;同时也显著增加了银杏叶片中单宁、萜类化合物和油松单宁、总酚的含量。但是在2007生长季中,这些物质的增幅相对2006生长季CO2处理减缓。高浓度CO2处理对银杏、油松叶可溶性蛋白含量和银杏叶中黄酮化合物含量的影响在两个生长季中变化不同:在2006生长季中高浓度CO2处理增加了银杏、油松叶可溶性蛋白含量,降低了银杏叶中黄酮化合物含量;在2007生长季中则降低了银杏、油松叶中可溶性蛋白含量,增加了银杏叶黄酮化合物含量。 2. O3倍增处理在2006、2007两个生长季中都有降低银杏、油松叶中淀粉、可溶性糖、可溶性蛋白含量和银杏叶中单宁、黄酮化合物含量的趋势;同时, O3倍增处理在两个生长季上都增加了银杏叶中萜类化合物和油松单宁、总酚化合物的含量。这表明次生代谢物质对高浓度O3处理的响应由于次生代谢物质的种类和所属植物种类的不同而不同。 3. 高浓度CO2和O3复合处理在2006和2007生长季上对银杏、油松的影响与单因子CO2处理类似。在复合作用中,单因子O3带来的光合产物下降的现象消失,银杏和油松的初生代谢产物都高于对照水平;同时,复合作用下次生代谢物质的变化也与单因子CO2处理一致。这表明在复合作用对银杏、油松次生代谢产物的影响主要通过CO2抵消O3对光合作用的抑制来实现,同时也说明CO2对银杏、油松次生代谢的影响强于O3的影响。高浓度CO2能够保护植物免受高浓度O3的伤害。 4. CO2倍增处理和复合处理增加了银杏和油松叶次生代谢物质的含量,这不仅能够增强银杏和油松对环境因子的抵御能力,而且还会增加植物对碳的同化作用,从而增加其对大气CO2的吸收;同时,由于次生代谢物质的抗菌能力,银杏和油松叶内次生代谢物质的增加有可能会减缓其凋落物在土壤中的降解,从而增加土壤碳“汇”。

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为了揭示UV-B辐射(11.66KJ/m2.d)和CO2浓度倍增复合作用对树木幼苗次生代谢产物变化规律及其对生长发育的影响,在室外用开顶箱,对白桦、红皮云杉和红松幼苗进行了模拟研究。结果表明,三种幼苗针叶片酚类含量增幅和变化趋势均不同。白桦类黄酮含量和305nm吸收值变化不大,红皮云杉和红松后期增加明显。白桦总黄酮和邻苯二酚含量增幅大于红皮云杉和红松。白桦和红松Chl和Car含量呈下降趋势,红皮云杉后期略有增加。白桦休眠侧芽极性小的酚类物质增加明显,根系酚类略有增加,枝条酚类无变化。红松越冬侧芽酚类和邻苯二酚含量增加明显。复合处理使三种幼苗PAL活性增加。酚类物质含量与其清除O-2和OH的能力基本成量效关系。单位多酚清除OH能力,红皮云杉>红松>白桦;多酚与蛋白质结合能力,白桦>红松>红皮云杉;MDA增幅,红松>白桦>红皮云杉。三种幼苗SOD活性后期增加明显。邻苯二酚对Chl、SOD、CAT活性和PSII有破坏作用。白桦酚类物质对SOD和CAT活性有破坏作用。复合处理对高生长抑制的程度白桦大于红松,而对红皮云杉影响不显著,体现UV-B和CO2处理的相互抵消作用。白桦根部生物量增加。红松针叶伸长受到抑制。可见,UV-B和CO2处理诱导的次生产物与幼苗生长发育有关。

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Marine sponges have been an abundant source of new metabolites in recent years. The symbiotic association between the bacteria and the sponge has enabled scientists to access the bacterial diversity present within the bacterial/sponge ecosystem. This study has focussed on accessing the bacterial diversity in two Irish coastal marine sponges, namely Amphilectus fucorum and Eurypon major. A novel species from the genus Aquimarina has been isolated from the sponge Amphilectus fucorum. The study has also resulted in the identification of an α–Proteobacteria, Pseudovibrio sp. as a potential producer of antibiotics. Thus a targeted based approach to specifically cultivate Pseudovibrio sp. may prove useful for the development of new metabolites from this particular genus. Bacterial isolates from the marine sponge Haliclona simulans were screened for anti–fungal activity and one isolate namely Streptomyces sp. SM8 displayed activity against all five fungal strains tested. The strain was also tested for anti–bacterial activity and it showed activity against both against B. subtilis and P. aeruginosa. Hence a combinatorial approach involving both biochemical and genomic approaches were employed in an attempt to identify the bioactive compounds with these activities which were being produced by this strain. Culture broths from Streptomyces sp. SM8 were extracted and purified by various techniques such as reverse–phase HPLC, MPLC and ash chromatography. Anti–bacterial activity was observed in a fraction which contained a hydroxylated saturated fatty acid and also another compound with a m/z 227 but further structural elucidation of these compounds proved unsuccessful. The anti–fungal fractions from SM8 were shown to contain antimycin–like compounds, with some of these compounds having different retention times from that of an antimycin standard. A high–throughput assay was developed to screen for novel calcineurin inhibitors using yeast as a model system and three putative bacterial extracts were found to be positive using this screen. One of these extracts from SM8 was subsequently analysed using NMR and the calcineurin inhibition activity was con rmed to belong to a butenolide type compound. A H. simulans metagenomic library was also screened using the novel calcineurin inhibitor high–throughput assay system and eight clones displaying putative calcineurin inhibitory activity were detected. The clone which displayed the best inhibitory activity was subsequently sequenced and following the use of other genetic based approaches it became clear that the inhibition was being caused by a hypothetical protein with similarity to a hypothetical Na+/Ca2+ exchanger protein. The Streptomyces sp. SM8 genome was sequenced from a fragment library using Roche 454 pyrosequencing technology to identify potential secondary metabolism clusters. The draft genome was annotated by IMG/ER using the Prodigal pipeline. The Whole Genome Shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession AMPN00000000. The genome contains genes which appear to encode for several polyketide synthases (PKS), non–ribosomal peptide synthetases (NRPS), terpene and siderophore biosynthesis and ribosomal peptides. Transcriptional analyses led to the identification of three hybrid clusters of which one is predicted to be involved in the synthesis of antimycin, while the functions of the others are as yet unknown. Two NRPS clusters were also identified, of which one may be involved in gramicidin biosynthesis and the function of the other is unknown. A Streptomyces sp. SM8 NRPS antC gene knockout was constructed and extracts from the strain were shown to possess a mild anti–fungal activity when compared to the SM8 wild–type. Subsequent LCMS analysis of antC mutant extracts confirmed the absence of the antimycin in the extract proving that the observed anti–fungal activity may involve metabolite(s) other than antimycin. Anti–bacterial activity in the antC gene knockout strain against P. aeruginosa was reduced when compared to the SM8 wild–type indicating that antimycin may be contributing to the observed anti–bacterial activity in addition to the metabolite(s) already identified during the chemical analyses. This is the first report of antimycins exhibiting anti–bacterial activity against P. aeruginosa. One of the hybrid clusters potentially involved in secondary metabolism in SM8 that displayed high and consistent levels of gene–expression in RNA studies was analysed in an attempt to identify the metabolite being produced by the pathway. A number of unusual features were observed following bioinformatics analysis of the gene sequence of the cluster, including a formylation domain within the NRPS cluster which may add a formyl group to the growing chain. Another unusual feature is the lack of AT domains on two of the PKS modules. Other unusual features observed in this cluster is the lack of a KR domain in module 3 of the cluster and an aminotransferase domain in module 4 for which no clear role has been hypothesised.