Relative quantification of chrysanthemum yellows (16Sr I) phytoplasma in its plant and insect host using real-time polymerase chain reaction

A real-time polymerase chain reaction (PCR) method for the quantification of chrysanthemum yellows (CY) phytoplasma DNA in its plant (Chrysanthemum carinatum) and insect (Macrosteles quadripunctulatus) host is described. The quantity of CY DNA was measured in each run relative to the amount of host DNA in the sample. Primers and a TaqMan probe for the specific PCR amplification of phytoplasma DNA were designed on a cloned CY-specific ribosomal fragment. Primers and TaqMan probes were also designed on sequences of the internal transcribed spacer region of the insect’s ITS1 rDNA and of the plant’s 18S rDNA for amplification from C. carinatum and M. quadripunculatus, respectively. Absolute quantification of CY DNA was achieved by comparison with a dilution series of the plasmid containing a CY 16S rDNA target sequence. Absolute quantification of plant and insect DNAs was achieved by comparison with a dilution series of the corresponding DNAs. Quantification of CY DNA in relation to host DNA was finally expressed as genome units (GU) of phytoplasma DNA per nanogram of host (plant or insect) DNA. Relative quantification avoided influences due to different yields during the DNA extraction procedure. The quantity of CY DNA was about 10,000–20,000 GU/ng of plant DNA and about 30,000–50,000 GU/ng of insect DNA. The method described could be used to phytoplasma multiplication and movement in different plant and insect hosts.     

3种菊花病毒/类病毒实时荧光定量RT-PCR检测体系的构建与准确性评价

菊花容易受到病毒感染而造成品质下降,目前国内对菊花病毒的检测主要根据外观表现或者定性PCR检测,无法准确判定病毒载量。为构建一种可同时用于检测菊花B病毒(Chrysanthemum virus B,CVB)、番茄不孕病毒(Tomato aspermy virus,TAV)和菊花褪绿斑驳类病毒(Chrysanthemum chloritic mottle viroid,CChMVd)的实时荧光定量RT-PCR检测方法,本研究分别以保守区域作为靶标设计相应的引物探针,通过优化扩增体系中CVB、TAV、CChMVd 3种病毒/类病毒探针浓度、引物浓度、Mg²⁺浓度、dNTPs浓度,摸索扩增程序中反转录时间、退火温度和扩增循环数,构建了一种可同时用于CVB、TAV、CChMVd的3重实时荧光定量RT-PCR检测体系,优化后的扩扩增体系中CVB、TAV和CChMVd的探针浓度分别为100 nmol/L、120 nmol/L和80 nmol/L,引物浓度分别为200 nmol/L、240 nmol/L和160 nmol/L,Mg²⁺浓度为3.0 mmol/L;dNTPs浓度200μmol/L;最适反转录时间为25 min,退火温度为60℃,循环数为40。敏感性实验结果表明,该反应体系对3种病毒/类病毒的敏感性为1.0×¹⁰3拷贝/mL,敏感性好;定量线性范围为1.0×¹⁰3拷贝/mL~1.0×¹⁰10拷贝/mL,线性范围宽;特异性好,对菊花矮化类病毒、烟草花叶病毒和黄瓜花叶病毒核酸检测结果为阴性;对1.0×¹⁰4拷贝/mL的低浓度参考品平行检测10次,定量结果lg值偏差(CV%)为4.81%,重复性好。在南京农业大学"中国菊花种质资源保存中心"基地随机选择菊花20株进行本研究试剂检测,检出6例CVB病毒株和4例TAV病毒株,其病毒载量为2.5×¹⁰4拷贝/mL~5.5×¹⁰7拷贝/mL,随机选择1株CVB病毒株定量PCR,产物进行TA克隆后经测序与NCBI Blast比对,其与MH678704.1的同源性为100%。因此,本研究建立了一种能同时检测CVB、TAV、CChMVd 3种菊花常见病毒/类病毒的灵敏、快速、可定量的检测方法。     

化肥减量配施有机肥对药用菊花产量、品质和药理活性的影响

采用田间小区试验,设置5个有机肥无机肥配施处理(100%化肥和14%、28%、56%、84%有机肥替代化肥处理),测定各处理对药用菊花农艺性状、产量、矿质元素吸收、有效成分含量的影响。并采用酶标仪和MTT试剂盒测定不同处理菊花水提物体外抗氧化活性及对H₂O₂致损的LO2肝细胞的保护作用。结果表明: 与100%化肥处理相比,化肥配施有机肥可以保证药用菊花产量,甚至低比例配施处理(14%有机肥替代化肥)还可以增产达8.3%。随着化肥减量配施有机肥比例的提高,菊花花中N、Mg含量呈上升趋势,而Ca和P含量分别在56%和28%有机肥替代处理有最大值。化肥减量配施有机肥可以显著增加药用菊花中绿原酸、木犀草苷和3,5-O-二咖啡酰基奎宁酸的含量,各成分含量随着有机肥比例的升高呈逐渐上升的趋势,上升幅度分别为3.3%～12.8%、15.7%～30.1%和9.5%～29.7%。各处理菊花水提液均有一定的体外抗氧化活性,且随着有机肥比例的升高呈先上升后下降的趋势;菊花水提液能显著提高H₂O₂致损的LO2肝细胞存活率,28%有机肥替代化肥处理细胞存活率最高,为91.2%,与模型组相比呈现极显著差异。综合产量、养分吸收、有效成分含量、体外抗氧化活性、对H₂O₂致损的LO2肝细胞的保护作用等指标,以及有机肥生态友好的特点,确定药用菊花栽培上以28%有机肥替代化肥的效果最佳。     

Characterization of Endo β-1,3-Glucanase IV from Flavobacterium dormitator var. glucanolyticae FA-5

Endo β-1,3-glucanase IV (E.C. 3.2.1.6, endo-1,3(4)-β-d-glucanase) from Flav. dormitator var. glucanolyticae FA-5 was shown to be a glycoprotein by gel filtration and sodium dodecyl sulfate gel electrophoresis. The carbohydrate moiety was composed of 17 hexose units. The enzyme had an apparent molecular weight of 3.3 x 10⁴, determined by gel filtration, sodium dodecyl sulfate gel electrophoresis and ultracentrifugation. The enzyme showed maximum reactivity at pH 6.0 and 6.5 for living yeast cells and laminaran, respectively. The enzyme predominantly released laminaripen-taose from a variety of linear β-1,3-glucans and showed transglucanosylation activity. The amino acid composition of the enzyme and some of its physicochemical and enzymatic properties are described.     

Oxidative stress and antioxidant activity as the basis of senescence in chrysanthemum florets

Stems of chrysanthemum (Chrysanthemum morifolium Ramat.) cv. Maghi were harvested when half of the buds showed colour and were put in distilled water at 21°C. Flowers showed visible senescence symptoms after 12–15 d. Reactive oxygen species (ROS) concentration and lipid peroxidation increased from young floret stage to the senescent stage. Activities of superoxide dismutase (SOD), ascorbate peroxidase (APX), peroxidase (POD) and catalase (CAT) showed uniform increases from young floret through to the mature stage and thereafter, declined. Among the SOD isoforms, Fe-SOD and Cu/Zn-SOD were induced during the onset of senescence. Similarly different isoforms of APX and glutathione reductase (GR) also appeared during the senescence process. The capacity of the antioxidative defence system increased during the onset of senescence but the imbalance between ROS production and antioxidant defences ultimately led to oxidative damage. It is proposed that a decrease in the activity of a number of antioxidant enzymes that normally prevent the build up of free radicals can at least partially account for the observed senescence of chrysanthemum florets.     

热激锻炼诱导菊花耐热性研究

以菊花(Chrysanthemum morifolium)叶片和花瓣为试验材料,在38℃下对其进行5 h的热激锻炼,再于50℃下分别进行0、0.5、1.0、1.5、3.0 h的高温胁迫,然后对其细胞膜透性、叶绿素、丙二醛(MDA)和蛋白质含量动态变化及5′-核苷酸酶的活性进行了测定.结果表明,热锻炼的菊花叶片电解质渗漏率相对较小,叶片叶绿素含量比对照下降的慢,5′-核苷酸酶活性比对照高,MDA含量也相对较低,而且花瓣中可溶性蛋白质保持了相对较高的含量,说明热锻炼诱导菊花获得了一定的耐热性.     

种植茼蒿对蚕豆苜蓿蚜的田间控制作用

[目的] 探讨不同生育期和不同种植方式的茼蒿对蚕豆蚜虫的诱集作用,为利用茼蒿控制蚕豆蚜虫提供理论依据。[方法] 在蚕豆田四周种植不同生育期（幼苗期、现蕾期、开花期）和不同行数（1行、2行）的茼蒿,观察不同处理的蚕豆田有蚜株率和蚜害等级,各处理设在互不干扰的小区内进行。[结果] 蚕豆四周种植不同生育期茼蒿后,蚕豆上有蚜株率和蚜害等级比例存在显著差异,且与茼蒿的生育期有明显的相关性,各处理有蚜株率从低到高分别为茼蒿开花期（28.33%） < 现蕾期（41.67%） < 幼苗期（55.00%）,并均显著低于对照（63.33%）;种植不同生育期茼蒿后,各处理蚕豆蚜害等级也不同,5级蚜害在种植开花期茼蒿处理后仅为5.00%,现蕾期为23.33%,幼苗期为33.33%,对照蚕豆上蚜害最高,达40.00%。分别种植1行（33.33%）和2行（23.33%）茼蒿后,最高有蚜株率均显著低于对照（66.67%）,低蚜害等级比例明显增高,高蚜害比例明显下降,且种植2行的效果更佳。[结论] 开花期的茼蒿对蚕豆蚜虫诱集作用最强,种植2行开花期茼蒿可以有效降低蚕豆蚜虫为害。在蚕豆生产上,种植茼蒿可以作为蚕豆蚜虫生态防控的重要手段之一。     

Spectral Filters and Temperature Effects on the Growth and Development of Chrysanthemums under Low Light Integral

The influence of altered light quality on the growth and development of chrysanthemum (cvs. Snowdon and Bright Golden Ann), was investigated in three different glasshouse temperatures i.e. 15, 20 or 24°C under low light levels. Five different colour filters i.e. blue and red absorbing (088), Blue absorbing (101), two partially blue absorbing (109 and 110) and Red absorbing (117) were tested, with clear polythene as a control. As in high light conditions, filters as well as temperature under low light levels significantly affected different growth parameters. Filters and temperatures significantly affected plant height and internode length, indicating that in chrysanthemum these were regulated by the action of phytochrome as well as a blue acting photoreceptor (cryptochrome). Time to flowering was affected by a combined action of phytochrome and cryptochrome since filters with blue transmission and high phytochrome photoequilibrium resulted in early flowering. The data were subjected to multiple regression and simple models were constructed to predict the influence of spectral quality on plant height, internode length and time to flowering in chrysanthemum. The models were then applied to simulate the potential benefits spectral filters used for green house cladding and regulation of plant growth under them.