995 resultados para Artemisia frigida


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Question: How do interactions between the physical environment and biotic properties of vegetation influence the formation of small patterned-ground features along the Arctic bioclimate gradient? Location: At 68° to 78°N: six locations along the Dalton Highway in arctic Alaska and three in Canada (Banks Island, Prince Patrick Island and Ellef Ringnes Island). Methods: We analysed floristic and structural vegetation, biomass and abiotic data (soil chemical and physical parameters, the n-factor [a soil thermal index] and spectral information [NDVI, LAI]) on 147 microhabitat releves of zonalpatterned-ground features. Using mapping, table analysis (JUICE) and ordination techniques (NMDS). Results: Table analysis using JUICE and the phi-coefficient to identify diagnostic species revealed clear groups of diagnostic plant taxa in four of the five zonal vegetation complexes. Plant communities and zonal complexes were generally well separated in the NMDS ordination. The Alaska and Canada communities were spatially separated in the ordination because of different glacial histories and location in separate floristic provinces, but there was no single controlling environmental gradient. Vegetation structure, particularly that of bryophytes and total biomass, strongly affected thermal properties of the soils. Patterned-ground complexes with the largest thermal differential between the patterned-ground features and the surrounding vegetation exhibited the clearest patterned-ground morphologies.

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Antibiotic resistance has emerged as a severe problem in hospital-acquired infectious disease. The Gram-negative bacterium Pseudomonas aeruginosa is found to cause secondary infection in immune-compromised patients. Unfortunately, it is resistant to virtually all β-lactam antibiotics such as penicillin, cephalosporin and others. Researchers are seeking for new compounds to treat several antibiotic-resistant bacterial strains. Artemisia plant extracts are commonly used for their therapeutic properties by natives throughout dry regions of North and South America. Here, they are administered as an alternative medicine for stomach problems and other complex health issues. In this study, the antimicrobial effects of plant extracts from several Artemisia species as well as compounds dehydroleucodine and dehydroparishin-B (sesquiterpenes derived specifically from A. douglasiana) were used as treatments against the pathogenicity effects of P. aeruginosa. Results showed that both compounds effectively inhibit the secretion of LasB elastase, biofilm formation and type III secretion, but fail to control LasA protease. This is a significant observation because these virulent factors are crucial in establishing P.aeruginosa infection. The results from this study signify a plausible role for future alternative therapy in the biomedical field, which recommends DhL and DhP can be studied as key compounds against bacterial infections of Pseudomonas aeruginosa.

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To enhance the therapeutic efficacy and reduce the adverse effects of traditional Chinese medicine, practitioners often prescribe combinations of plant species and/or minerals, called formulae. Unfortunately, the working mechanisms of most of these compounds are difficult to determine and thus remain unknown. In an attempt to address the benefits of formulae based on current biomedical approaches, we analyzed the components of Yinchenhao Tang, a classical formula that has been shown to be clinically effective for treating hepatic injury syndrome. The three principal components of Yinchenhao Tang are Artemisia annua L., Gardenia jasminoids Ellis, and Rheum Palmatum L., whose major active ingredients are 6,7-dimethylesculetin (D), geniposide (G), and rhein (R), respectively. To determine the mechanisms underlying the efficacy of this formula, we conducted a systematic analysis of the therapeutic effects of the DGR compound using immunohistochemistry, biochemistry, metabolomics, and proteomics. Here, we report that the DGR combination exerts a more robust therapeutic effect than any one or two of the three individual compounds by hitting multiple targets in a rat model of hepatic injury. Thus, DGR synergistically causes intensified dynamic changes in metabolic biomarkers, regulates molecular networks through target proteins, has a synergistic/additive effect, and activates both intrinsic and extrinsic pathways.

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The seasonal occurrence of sea ice that annually covers almost half the Baltic Sea area provides a unique habitat for halo- and cold temperature-tolerant extremophiles. Baltic Sea ice biology has more than 100 years of tradition that began with the floristic observation of species by the early pioneers using light microscopic techniques that were the only thing available at the time. Since the discovery of life within sea ice, more technologies have become available for taxonomy. Electron microscopy and genetic evidence have been used to identify sea ice biota revealing increased numbers of taxa. Meanwhile ecologists have used light microscopic cell enumeration in addition to the chemical and physical properties of sea ice in attempts to explain the food web structure of sea ice and its functions. Thus, during the Baltic winter, the sea ice hosts more abundant and diverse microbial communities than the water column beneath it. These communities are typically dominated by autotrophic diatoms together with a diverse assortment of dinoflagellates, auto- and heterotrophic flagellates, ciliates, metazoan rotifers and bacteria, which are mostly responsible for the recycling of nutrients. This thesis comprises ecological and systematic studies. In addition to the results of the previous studies carried out on landfast ice, the data presented here provide new insight into the spatial distribution of pelagial sea ice, which has remained largely unexplored. The studies reveal spatial heterogeneity in the pelagial sea ice of the Gulf of Bothnia. There were mismatches in chlorophyll-a concentrations and in photosynthetic efficiencies of the communities studied. The temporal succession was followed and experimental studies performed investigating the community responses towards increased or decreased light in landfast ice in the Gulf of Finland. The systematic studies carried out with established dinoflagellate cultures revealed a new resting cyst belonging to common sea ice dinoflagellate, Scrippsiella hangoei (Schiller) Larsen 1995. The cyst can be used to explain the overwintering of this species during prolonged periods of darkness. The dissimilarities and similarities in the material isolated from the sea ice called for description of a new subspecies Heterocapsa arctica ssp. frigida. The cells obtained in the cultured material were unlike those of the previously described species, necessitating description of ssp. frigida. As a result of its own unique habitus, the subspecies had been noted by Finnish taxonomists during the past three decades and thus its annual occurrence and geographical distribution in the Baltic Sea. This illustrates how combining ecology and systematics increases our understanding of organisms.

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Increased anthropogenic loading of nitrogen (N) and phosphorus (P) has led to an eutrophication problem in the Baltic Sea, and the spring bloom is a key component in the biological uptake of increased nutrient concentrations. The spring bloom in the Baltic Sea is dominated by both diatoms and dinoflagellates. However, the sedimentation of these groups is different: diatoms tend to sink to the sea floor at the end of the bloom, while dinoflagellates to a large degree are been remineralized in the euphotic zone. Understanding phytoplankton competition and species specific ecological strategies is thus of importance for assessing indirect effects of phytoplankton community composition on eutrophication problems. The main objective of this thesis was to describe some basic physiological and ecological characteristics of the main cold-water diatoms and dinoflagellates in the Baltic Sea. This was achieved by specific studies of: (1) seasonal vertical positioning, (2) dinoflagellate life cycle, (3) mixotrophy, (4) primary production, respiration and growth and (5) diatom silicate uptake, using cultures of common cold-water diatoms: Chaetoceros wighamii, C. gracilis, Pauliella taeniata, Thalassiosira baltica, T. levanderi, Melosira arctica, Diatoma tenuis, Nitzschia frigida, and dinoflagellates: Peridiniella catenata, Woloszynskia halophila and Scrippsiella hangoei. The diatoms had higher primary production capacity and lower respiration rate compared with the dinoflagellates. This difference was reflected in the maximum growth rate, which for the examined diatoms range from 0.6 to 1.2 divisions d-1, compared with 0.2 to 0.3 divisions d-1 for the dinoflagellates. Among diatoms there were species specific differences in light utilization and uptake of silicate, and C. wighamii had the highest carbon assimilation capacity and maximum silicate uptake. The physiological properties of diatoms and dinoflagellates were used in a model of the onset of the spring bloom: for the diatoms the model could predict the initiation of the spring bloom; S. hangoei, on the other hand, could not compete successfully and did not obtain positive growth in the model. The other dinoflagellates did not have higher growth rates or carbon assimilation rates and would thus probably not perform better than S. hangoei in the model. The dinoflagellates do, however, have competitive advantages that were not included in the model: motility and mixotrophy. Previous investigations has revealed that the chain-forming P. catenata performs diurnal vertical migration (DVM), and the results presented here suggest that active positioning in the water column, in addition to DVM, is a key element in this species' life strategy. There was indication of mixotrophy in S. hangoei, as it produced and excreted the enzyme leucine aminopeptidase (LAP). Moreover, there was indirect evidence that W. halophila obtains carbon from other sources than photosynthesis when comparing increase in cell numbers with in situ carbon assimilation rates. The results indicate that mixotrophy is a part of the strategy of vernal dinoflagellates in the Baltic Sea. There were also indications that the seeding of the spring bloom is very important for the dinoflagellates to succeed. In mesocosm experiments dinoflagellates could not compete with diatoms when their initial numbers were low. In conclusion, this thesis has provided new information about the basic physiological and ecological properties of the main cold-water phytoplankton in the Baltic Sea. The main phytoplankton groups, diatoms and dinoflagellates, have different physiological properties, which clearly separate their life strategies. The information presented here could serve as further steps towards better prognostic models of the effects of eutrophication in the Baltic Sea.

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Homenaje a Ignacio Barandiarán Maestu / coord. por Javier Fernández Eraso, Juan Santos Yanguas

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利用发根农杆菌(Agrobacterium rhizogenes)1601,1000,1500,15834,A4,均成功地转化了中药青蒿(Artemisia annua L.)并且建立了pRi1601,pRi15834,pRiA4诱导的发根培养。pRi1601,pRi15834的发根诱导率比其它质粒高。太老或太幼的叶片不利子发根的诱导;发根主要从叶脉的伤口处萌发;带顶芽或带侧芽的叶片容易诱导根,但不一定是发根。光照有利于发根的诱导和发根的生长。以每个发根的“绝对生长速率”(Gtowth Ratio,GR)和绝对“侧根”数量(Number of Side Roots,NSR),通过大量的发根系的筛选,建立了8个发根系,1601-L-1, 1601-L-2, 1601-L-3, 1601-L-4, 15834-L-1, 1601-P-I, 16 01-P-2,15834-L-2。Southern分子检测表明,160l-1-1,1801-L-2, 1601-L-3,1601-L-4,1601-P-1,1601-P-2均为转化子。8个建立的发根系之间无论生长或者QHS的合成存在明显的差异。比较光/暗(16/8hrs),25℃条件下培养的16 01-L-1,1601-L-2,1601-L-3,1601-L-4,1601-P-l,和1601-P-2,其中16 01-L-3的生长最快,160l-L-1的生长最慢;但是,1601-L-1的QHS的含量最高(可达1. 048%),1601-1-3的QHS的含量最低。160Z-L-3,15834 -L-1和2583:1-L-2的生长速率相差不大。用盛有l000mLMS液体培养基的3000mL的锥形瓶扩大培养1601-L -3,15834-L-1和15834-L-2,转速为ll0rlpm,培养过程中发根容易形成发根球(Hairy Root Balis,HRB),HRB的形成严重影响发根的生长和QHs的合成,HpLC分析表明扩大培养发根中QHS的含量比较低。 改变MS基本培养基中的无机离子的浓度,研究不同无机离子对发根生长和QHS的合成的影响。 l、KN03为18.79×10-3M时有利于1601- L-1生长,为14. 84×10-3M时有利于QHS的合成。NH-4N0-3浓度在10.93-12. 49×10—3M范围内有利于1601-L-1生长,在0-20.62×10-3M范围内对QHS的合成影响不大,大于20. 62×lO-3M不利QHS的合成。培养基中NH-4+/N0-3-比值为0. 37-0. 4-0.52:1时有利于发根的生长,比值为0.52 - 0.58:1时有利于QHS的合成。 2、H-2P0-4-浓度为2.498×10-3M时有利于发根的生长在0-2. 498×l0-3M范围内,随着浓度的提高,促进发根的生长。培养基中的H2P4 -的浓度在0-1.249×lO-3M的范围内,随着浓度的提高,促进QHS的合成,为1.249×10-3M时QHS的含量最高。 3、培养基中最适16 01-L-1生长的Ca-2+浓度为0.198- 0.766×10-3M,大于或小于该浓度范围,显著地抑制发根的生长。但是,在0-3.695×10-3M范围内,随着培养基中Ca-2+浓度提高,促进QHS的合成,最适Ca-2+浓度为3.695×l0-3M。 4、培养基中不加Mg-2+时,完全抑制发根生长,在0. 142×10-3M-7.506×l0-3M浓度范围内,对发根生长影响没有明显的差别。但是,HPLC和UV分析发根中QHS含量,培养基中不加Mg-2+时,发根中QHS含量最高。 5、培养基中的Fe-2+浓度在0. 25 -1.0×10-3M范围内,同时有利于16 01- L-1的生长和QHS的形成。 6、培养基中最适合予16 01- L-3生长的KI浓度为2.5ppm,大于或小予该浓度均显著地抑制发根的生长,培养基中加入KI明显地降低发根中的QHS的含量。 7、H2BO3对l601-L-l生长影响不大,HPLC分析QHS的含量,培养基中的H3BO3浓度为100ppm和400ppm,QHS的含量分别为1.69mg/g和1.80mg/g(DW)。 8、Cu-2+对1601-L-3的生长影响显著,最适合1601-L-3生长的Cu-2+浓度为1.00ppm,在0 -1.00ppm的浓度范围内,随着培养基中的Cu+浓度的提高,发根的生物量不断增加。培养基中QHS合成的最适Cu2+浓度为0.05ppm,大于或小于该浓度均显著地抑制发根中QHS的合成。 比较光培养和暗培养对发根生长的影响,结果表明光照明显地促进1601-L-l的生长,暗培养明显不利于发根的生长。最适合于发根生长的温度为25℃,大于35℃显著地抑制发根的生长,影响发根的根尖细胞的正常分裂。 改变培养基中的蔗糖浓度和在发根培养的不同时期给培养基中添加蔗糖,试验结果表明蔗糖作为碳源对1601-L-3和1601-L-1的生长具有显著的影响。 (1)培养基中缺少蔗糖显著地抑制发根的生长。 (2)发根培养的前5天时间内,蔗糖浓度为30- 60glL昀培养基最有利于发根的生长,50glL的培养基中的发根生长最快,培养基中的蔗糖浓度大于60g/L小于30g/L时,发根的生物量增加较少。 (3)发根培养至第15天时,蔗糖浓度为60g/L的培养基最有利予发根的生物量的增加。发根培养至30天时,蔗糖浓度为60-90g/L的培养基,发根的生物量的增加相差不大,但是为蔗糖浓度为30-40g/L的培养基中的发根生物量一倍。 (4)发根培养过程中,分别于第5和15天给蔗糖浓度为30g/L的培养基中添加一次或二次蔗糖,使培养基中的蔗糖终浓度相当于60g/L或90g/L,培养至30天时,添加蔗糖的培养基中的发根的干重生物量相当于不添加蔗糖培养基中的发根生物量一倍,相当于初始蔗糖浓度为60g/L和90g/L培养基中发根的生物量。 (5)随着培养基中蔗糖浓度的提高,发根干重/鲜重比显著增加。培养基中的蔗糖的消耗量与发根生物量的增加呈正相关,蔗糖消耗越多,发根生物量的增加越大。 比较pH值对发根生长和QHS合成的影响表明,灭菌前pH值在5.O-6.5范围内的培养基适合予1601-L-1的生长,小于5.O不利于发根的生长,pH5.8有利于1601-1-1生长和QHS的生物合成。发根收获时培养基中的pH值一般为4.5-5.2. pH7.O抑制发根的生长,pHl0.O对发根具有强烈的致死作用。发根在培养过程中,对培养基中的pH值具有显著的调节作用,发根能在很短的时间内(24- 48hrs)使pl:l值为5.8、6.4、7.0培养基降低到pH4. 5-5.2,pH为5.8的培养基有利于QHS合成。 比较不同基本培养基对发根生长和QHS合成的影响,试验结果表明N6、DCR、Litvay培养基有利于1601-L-1的生长,WS、White、B5培养基不利于发根的生长。DCR培养基中的QHS含量最高。 根据三水平试验选用三水平正交表来安排试验的原则,选用三水平正交表L7(3-),研究多因子效应对发根生长和QHS合成的影响,试验结果表明,Mg2+,Fe2+,Mn-2+,NH4NO3,KN03 ,KI,Ca-2+为发根生长的主要因子,NH4N03,KNOs,Mg2+,Ca2+,肌醇为QHS合成的主要因子。 通过TLC分析发根中QHS和其它化学成分,同时比较发根和无菌苗及野生植株的化学成分,发根和无菌苗均能合成包括QHS在内的野生青蒿叶片中的大部分非挥发性的化台 物。 研究青蒿植株在发育过程中QHS的含量的变化以及发根、无菌苗和野生青蒿中QHS的合成,HP分析结果表明,l、不同的单株青蒿之间的QHS量相差很大。2、同一植株幼 叶的QHS含量比老叶的QHS含量高。3、不同单株青蒿之间达到最高QHS含量的时间不一样,开花期或开花之前。4、无菌苗(带根)或者不带根丛生芽均能合成QHS,但是带根的无菌蕾的QHS量比丛生芽中的QIS的含量高。5、不同发根农杆菌转化的发根系1601-L-1和15834-L-1都能合成QHS。

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本论文由三部分内容组成,一、药用青蒿的遗传转化,即根癌农杆菌和发 根农杆菌介导的转化系统的建立及其影响参数的研究。二、青蒿素生物合成的 分子调控。三、倍半萜生物合成相关基因的克隆。 一、药用青蒿的遗传转化。建立了Ri质粒介导和Ti质粒介导的两种转基因系统, 其中Ri质粒介导青蒿转基因系统的建立是国际上首次报道;以GFP基因为报 告基因,首次获得高效表达的青蒿转绿色荧光蛋白基因的丛生芽,并对GFP基 因的表达进行了组织和细胞水平的定位。此外,对影响两种转基因系统的主要 参数进行了较为详细的研究。上述研究为青蒿素生物合成的分子调控奠定了坚 实的基础。 二、青蒿素生物合成的分子调控。为探索提高青蒿植株或组织和器官中的青蒿 素含量,首次以棉花中克隆的杜松烯合成酶和法呢基焦磷酸合成酶的 cDNA 为 目的基因导入青蒿,对青蒿中青蒿素的生物合成进行了分子调控研究的尝试。 通过已建立的两种转基因系统,将从棉花中克隆的杜松烯合成酶和法呢基焦磷 酸合成酶的 cDNA 导入青蒿,获得转基因发根和转基因植株。结果表明,外源 基因的表达能够影响青蒿素的生物合成,其中法呢基焦磷酸合成酶基因的过量 表达能够促进青蒿素的生物合成,提高转基因发根和植株中的青蒿素的含量。 转基因发根F-26系中青蒿素含量最高达3.01 mg/g.DW,与对照相比青蒿素含量 提高3~4倍;转基因植株的青蒿素含量最高达10.08 mg/g.DW,与对照相比, 转基因植株的青蒿素产物提高2~3倍。此外,研究还表明,在转基因的发根C -37株系中,外源杜松烯合成酶基因的导入和表达可能相应地促进青蒿转基因 发根自身的法昵基焦磷酸基因的表达。 三、倍半萜生物合成相关基因的克隆。采用 RT-PCR 技术,从马铃薯 (Solanum tuberosum L.) 幼叶中克隆了 HMGRII 亚基因家族的一个新的成员 HMGR-c2(GenBank accession No.AF 096838Southem);杂交分析表明,该基因至少以 两个拷贝以上形式存在于马铃薯基因组中;RT-PCR分析表明,HMGR -c2的 表达在幼苗期无组织特异性,广泛地存在于根、茎、叶等组织中。以青蒿001 株系的苗期叶片为材料,构建了青蒿苗期的λgtll cDNA文库,以PCR筛库方 法从青蒿中克隆一个法呢基焦磷酸合成酶cDNA (Artfps2 GenBank accession No. AF136602)和一个HMGR cDNA(GenBank accession No.AF142473);以青蒿 025株系的苗期叶片为材料,构建了青蒿苗期部分质粒文库以 PCR 筛库方法从 青蒿中克隆一个法昵基焦磷酸合成酶 cDNA (Artfpsl GenBank accession No.AF112881);此外,还从青蒿中克隆了倍半萜合成酶的 cDNA 片段(GenBank accession No.AF156854)。其中青蒿倍半萜合成酶基因的克隆是目前国际上本研 究领域最受关注的焦点和难点之一。至此,本研究已将与青蒿素生物合成相关 的三个重要的关键酶基因基本克隆,这无疑将加速青蒿素生物合成的基础和应 用研究的进程。

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本论文主要包括以下两部分内容: 一、真菌诱导子对青蒿发根生长和青蒿素生物合成的影响 用3种真菌诱导子[大丽花轮枝孢(Verticillium dahliae Kleb.)、葡枝根霉(Rhizopus stolonifer (Ehrenb. ex Fr.) Vuill)和束状刺盘孢(Colleto trichumdematium (Pers.) Grove)]分别处理青蒿(Ar temisia annuaL.)的发根,这3种真菌诱导子均能促进发根中青蒿素的合成,其中以大丽花轮枝孢的诱导效果最好;对细胞生长均没有明显影响。经大丽花轮枝孢处理的发根中青蒿素含量达1. 12 mg/gDW,比对照(0. 77 mg/g DW)提高45%。诱导子的作用效果与诱导子浓度、诱导子作用时间及发根的生长状态有关。对大丽花轮枝孢来说,诱导子作用的最适浓度为每毫升培养基含糖0.4 mg;发根在指数生长末期对诱导作用最敏感:在加入诱导子4d后收获发根,发根中的青蒿素含量最高。 二、早花基因FPF1、co对青蒿开花时间的影响及开花与青蒿素生物合成的相关性 1.将来源于拟南芥的早花基因Flowering Promoting Factorl (FPFl)插入到植物表达载体pBI121中,构建CaMV 35S启动子控制下含FPFl基因的植物表达载体pBI121FPF/,用含有pBI121FPF/质粒的根癌农杆菌(Agrobacterium tumefaciens)LBA4404感染青蒿(Artemisia annua L.)叶片并诱导丛生芽,经卡那霉素筛选,获得转基因抗性植株。PCR、 PCR-Southem blot及Southern blot检测表明,外源基因FPFI已整合到青蒿基因组中:RT-PCR及RT-PCR Southern blot分析表明,外源基因在转录水平上已有表达。在短日照条件下,FPF1转基因植株的开花时间较对照提前20天左右,但提早开花的转基因植株与未开花的对照其青蒿素含量无明显差异,即提早开花并不能使开花植株的青蒿素含量有所提高,开花与青蒿素合成之间可能没有直接的关系。 2.将拟南芥的早花基因CONSTANS (CO)置于CaMV 35S启动子之下,通过根癌农杆菌(Agrobacterium tumefaciens)LBA4404介导转入青蒿(Artemisia annuaL.),使之在青蒿中表达,并得到了抗性植株。PCR、PCR-Southem blot及Southemblot检测表明,外源基因co已整合到青蒿基因组中;RT-PCR及RT-PCR Southemblot分析表明,外源基因在转录水平上已有表达。在短日照条件下,co转基因植株的开花时间较对照提前2周左右,但提早开花的转基因植株的青蒿素含量与未丌花的对照无明显差异,即植株开花前青蒿素含量的提高并不是由于开花本身引起的,再次证明,开花与青蒿素合成之间可能没有直接的关系。

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第一部分:青蒿开花与青蒿素生物合成相关性的研究 青蒿素是从中药青蒿中分离出的倍半萜内酯化合物,目前是世界上唯一有效的治疗脑型疟疾和抗氯喹恶性疟疾的药物。青蒿植株中青蒿素含量在开花期最高,但是目前尚不清楚开花与青蒿素生物合成的关系。为此,我们用光周期(短日照)诱导青蒿提前开花,不仅同时获得了开花与不开花的青蒿植株,而且还成功地在同一植株上诱导部分分枝开花,另一部分分枝保持营养生长状态。这一实验体系为研究青蒿开花与青蒿素生物合成的相关性奠定了基础。实验结果表明,开花与不开花青蒿植株青蒿素含量有明显差异。开花植株的青蒿素含量在前2周内逐渐提高,第三周(开花期)达到最高,并保持一周左右,在随后的2周内下降。青蒿植株开花后,叶片便开始老化变黄,逐渐死亡。未开花青蒿植株的青蒿素含量动态在前三周内与开花植株类似,但是这种高青蒿素含量状态能保持较长时间,至少在随后的2周内没有下降。未开花植株的叶片依然保持绿色。这一结果表明,开花不是导致青蒿素含量提高的直接原因。 扫描电镜观察结果表明,幼嫩叶片上的毛状腺体( trichrome)结构是完整的,而在老化的叶片上,则观察到了相当比例(40-50%)破损的腺体。这可能是导致青蒿素含量下降的直接原因。 不同生态型青蒿对光周期的反应是不同的。在北京地区,本地青蒿在8月初便开始开花,而来自四川武陵的青蒿则要到9月份才能开花。根据这一特性,采用“南蒿北栽”的方法,能够使青蒿保持较长时间的营养生长状态,延长适于采收的时间。 第二部分:金丝桃和百金花二苯甲酮合酶基因的克隆,异源表达及功能分析 植物次生代谢物山屯酮( Xanthones)仅存在于龙胆科和藤黄科植物中。它们具有抑制单胺氧化酶,细胞毒素及抗肿瘤活性。 含有1 3个碳原子的二苯甲酮是山屯酮生物合成的中间产物,是由二苯甲酮合酶催化合成的,这一反应是山屯酮生物合成的关键步骤。二苯甲酮合酶已经在金丝桃和百金花细胞悬浮培养系统中检测到,并进行了细致的生化水平上的研究。本研究是在上述研究的基础上,进一步克隆该酶的基因,并进行异源表达及功能分析工作,以便更好地了解和调控山屯酮的生物合成。 用PCR和RT-PCR技术,从金丝桃cDNA文库和逆转录产物中分别克隆到一个基因HBPS1和HBPS2,从百金花cDNA文库中克隆到一个基因CBPS1。HBPS1含有1402个碱基,其开放阅读框架编码390个氨基酸,分子量为42.7 kDa,等电点为6.55。HBPS2含有1398个碱基,其开放阅读框架编码395个氨基酸,分子量为42.8 kDa,等电点为5.78。CBPS1含有1383个碱基,其开放阅读框架编码389个氨基酸,分子量为42.7 kDa,等电点为7.88。与GenBank中序列同源性比较结果表明:在氨基酸水平上,HBPS1与茶(Camellia sinensis)查尔酮合酶的同源性高达92%,HBPS2与萝卜(Raphanus sativus)查尔酮合酶的同源性为64%,CBPS1与茶(Camellia sinensis)查尔酮合酶的同源性为71%。HBPS1与HBPS2的同源性仅为62%。 将三个新克隆的基因的ORF整合到载体pGEX-G上的谷胱甘肽还原酶S基因下游,构建成转化质粒,并在大肠杆菌中诱导表达。结果表明,这三个基因的ORF片段均能被表达成约68 kDa的产物,这与期望的结果一致。 活性检测结果表明,HBPS1是查尔酮合成酶,其底物为香豆酰辅酶A和丙二酸单酰辅酶A,对这两种底物的亲和性KM分别为:香豆酰辅酶A 2.8μM,丙二酸单酰辅酶A,11.2μM。最适反应条件是350C,pH7.0,DTT浓度10 μM。 HBPS2是二苯甲酮合酶,其底物是苯甲丙氨酰辅酶A,和丙二酸单酰辅酶A,对这两种底物的亲和性KM分别为:苯甲丙氨酰辅酶A 2.4 μM,丙二酸单酰辅酶A 9.6μM。最适反应条件是350C,pH 6.5,DTT浓度50 μM。而CBPS1则没有检测到任何活性。从同一种植物中同时获得了查尔酮合酶和二苯甲酮合酶,对研究这两种十分相近的酶的差异表达,酶促反应机制等问题将非常有利。