北方设施条件下辣木及改良品种生长差异性分析

北方地区利用温室栽培辣木(Moringa oleifera Lam.)及其2个改良品种‘PKM1’和‘PKM2’,通过分析表观生长量、养分含量以及光合特性等指标的差异性,筛选适宜北方温室种植的辣木品种。结果表明:PKM1的高生长和增粗生长均显著快于辣木和PKM2(p0.05),在定干前(71 d)三者平均株高依次为115.7、80.2、81.0 cm,地径依次达17.47、13.27、15.08 mm。植株养分季节变化,PKM1养分状况要优于辣木和PKM2,在5月份,PKM1叶片中全氮(44.32 mg/g)、全钾(12.73 mg/g)含量显著高于其它2个品种(p0.05),全磷和可溶性糖含量品种间无显著性差异;7月份,PKM1可溶性糖显著高于其它2个品种;光合特性分析,3个品种在弱光条件下的光量子利用效率及光补偿能力差异不显著(p0.05),随着光强增加,光量子的转化能力出现显著性差异,PKM1的最大净光合速率(A_(max))显著高于辣木和PKM2(p0.05),最高达23.84μmol CO_2/(m~2·s)。可见,北方设施条件下,PKM1的生长速度、养分状况、光合能力均表现最好,较适宜北方温室栽培。     

茶悬浮培养细胞玻璃化超低温保存研究

为保存具有稳定代谢能力的优良茶细胞系,本文对茶叶悬浮培养细胞玻璃化法超低温保存进行了初步研究。结果表明:预培养以4d最佳,60%PVS2冰浴装载以20min最好,100%PVS2冰浴脱水处理60min最优,40℃复温解冻细胞存活率最高,采用这些参数进行完整试验的细胞存活率达到76%,初步建立了茶悬浮培养细胞玻璃化超低温保存的冷冻程序。     

铅污染对茶树生育及相关保护酶活性的影响

采用盆栽试验,选取龙井43和浙农117两个茶树品种,进行了铅污染对茶树生育及相关保护酶活性的影响研究。结果表明,在试验处理浓度范围内,铅能促进龙井43的生长;浙农117在160mg／kg铅处理浓度下,初期对生长有促进作用,之后作用消失。浙农117在铅浓度160mg／kg时,净光合速率已受影响;龙井43品种在160mg／kg浓度条件下还会对光合作用起到促进作用,430mg／kg铅处理浓度下对茶树光合作用产生抑制;随着铅污染浓度增加,浙农117的过氧化物酶和超氧歧化酶的活性均升高;龙井43的过氧化物酶活性先升高后降低,而超氧歧化酶的活性增强。     

壳聚糖在茶树上的应用效应

采用叶面喷施的方法，对壳聚糖在茶树上的应用效应进行了研究。结果表明，壳聚糖能促进茶树芽叶萌发和生长，提高茶叶产量，增加茶叶中水浸出物和氨基酸含量，降低酚氨比。壳聚糖对茶叶中茶多酚含量有一定的影响，而对咖啡碱影响不大。本试验所设置浓度范围内，150mg／kg是叶面喷施壳聚糖较适宜的浓度。     

乌龙茶种质资源种群遗传多样性AFLP评价

以银染法AFLP分子标记技术用5对引物组合对来自福建武夷山市、安溪县、台湾省和广东潮安县45份乌龙茶品种资源进行遗传多样性分析。结果表明,5对引物扩增出208条多态性条带,多态性为92.03%;最大遗传距离为0.481,最小遗传距离为0.124,种质资源间遗传多样性估值较高,达0.311。按照地理分布分组分析表明,种群内遗传多样性以武夷山最高,其次为安溪乌龙茶种质资源,以台湾的乌龙茶种质资源遗传多样性最小;种群间遗传相似性,以武夷山与安溪种群间最高,达0.9505,以台湾和潮安县类型间的相似性最低,相似性系数为0.77。构建的种间和种群间进化树表明,可将45份乌龙茶品种划分为二大类型,福建类型和广东潮安类型。结合种群间相似系数,提出乌龙茶种质资源与其加工工艺的演化路径是一致的,也是由武夷山向安溪再向台湾传播。     

Volatile Compounds in Two Camellia chrysantha （Hu） Tuyama Species

In the study,the volatile compounds in two Camellia chrysantha （Hu） Tuyama species were extracted and analysed by simultaneous steam distillation and extraction （SDE） and gas chromatography mass spectrometry （GC-MS）,respectively.The relative contents of the chemical constituents in the volatile components were quantified by peak area normalization and NIST database.A total of 60 volatile components were identified,45 for Camellia nitidissima and 26 for Camellia euphlebia.Aldehydes and acids were the most dominant volatiles in Camellia nitidissima,but for Camellia euphlebia there were hydrocarbons and ketones.Hexanoic acid,4-（2,6,6-trimethyl-1-cyclohexenyl）-3-buten-2-one,cis-2-decenal,4-[2,2,6-trimethyl-7-oxabicyclo [4.1.0] hept-1-yl]-3-buten-2-one,phenylacetaldehyde,eicosane,alpha-ionone,geranylacetone 2,6-di-tert-butyl-4-methylphenol,7,9-di-tert-butyl-1-oxaspiro[4,5] deca-6,9-diene-2,8-dioi and tetradecanal were both in two Camellia chrysantha （Hu）Tuyama species.     

Dynamics of nitrogen translocation from mature leaves to new shoots and related gene expression during spring shoots development in tea plants (Camellia sinensis L.)

The contribution of N remobilization is crucial for new shoots growth and quality formation during spring tea shoots development. However, the translocation mechanism of N from source leaves to sink young shoots is not well understood. In the present study, ¹⁵N urea was applied to mature tea leaves one week before bud break to track N remobilization in a field experiment. The dynamic changes in plant ¹⁵N abundance, contents of amino acids, and the expression levels of genes related to N metabolism and translocation were followed during the 18‐d development of new spring shoots until three expanding young leaves. The results showed that during the growth of new shoots the amount of ¹⁵N in the shoots increased, whereas the N_dff (N derived from ¹⁵N‐urea) in mature leaves decreased, showing that the foliar‐applied N in mature leaves was readily exported to new shoots. This process was found to be accompanied by decline of chlorophylls. In the mature leaves, expression CsATG18a and CsSAG12 involved in autophagy was dramatically induced (> 4‐fold) at approximately nine days after the bud breaking. The genes involved in the transformation of amino acids, including primarily CsGDH2, CsGDH4, CsGLT3, CsGS1;3, and CsASN2 were upregulated by > 3‐fold after bud breaking. The expression levels of CsATG8A, CsATG9, CsSAG12, CsGS1;1, CsGDH1, and CsAAP6 correlated negatively with the N_dff in mature leaves, but positively with ¹⁵N amount and total N amount in new shoots, suggesting these genes played important roles in N export from mature leaves. In the new shoots, the expression of most genes showed two defined peaks, one on six days and one on 12 days after bud breaking. The expression of CsGS2, CsASN3, CsGLT1, and CsAAP4 positively correlated with the ¹⁵N amount and total N amount in new shoots. These genes might be involved in the transport and re‐assimilation of N from mature leaves. The overall results demonstrated that the translocation of ¹⁵N from mature leaves to new spring shoots was regulated by the genes involved in autophagy, protein degradation, amino acid transformation and transport.     

金花茶对低温胁迫的生理响应及耐寒性分析

为探究金花茶幼苗对低温胁迫的生理响应及其耐寒性,本研究以2 a生金花茶幼苗为材料,进行6~-9℃低温胁迫处理,测定了细胞伤害率(CIR)、丙二醛(MDA)、过氧化物酶(POD)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、束缚水(BW)/自由水(FW)、脯氨酸(Pro)、可溶性糖(SS)等指标,并进行了低温半致死温度(LT₅₀)和抗寒生理指标相关性分析。结果表明,3~12 h的低温LT₅₀为-6.62~-3.94℃,且随着时间的延长而升高。随着温度的降低, CIR、SS含量及POD、CAT活性总体呈上升趋势, BW/FW、MDA、Pro含量呈先上升后下降趋势, SOD活性总体呈下降趋势;随着胁迫时间的延长,CIR含量呈上升趋势,3~-9℃的SOD活性、0~-9℃的POD活性、-6~-9℃的BW/FW比值呈下降趋势,6~-6℃的SS含量变化较小,-9℃的SS含量呈下降趋势。相关性分析表明,CIR可作为耐寒性鉴定的主要指标,BW、SS、SOD、POD、CAT可作为辅助指标。本研究结果为金花茶引种区域和耐寒性鉴定指标的确定提供了理论依据。     

茶树凋落叶浸提液对菘蓝生理生化的化感效应

为研究茶树凋落叶浸提液对菘蓝生长与生理生化的化感效应,以模拟自然条件下雨雾淋溶方式,采用不同浓度的茶树凋落叶浸提液(CK:0 mg·mL^-1、T1:6.25 mg·mL^-1、T2:12.5 mg·mL^-1、T3:25 mg·mL^-1 和T4:50 mg·mL^-1)处理菘蓝,测定其生长、抗氧化酶活性及其基因表达量、细胞膜损伤率以及丙二醛(MDA)、过氧化氢(H₂O₂)、渗透调节物质和次生代谢物含量的变化。结果表明,茶树凋落叶浸提液对菘蓝生长表现出“低促高抑”的浓度效应,与CK相比,T1对菘蓝生长具有一定的促进作用,而浸提液浓度超过菘蓝的耐受阈值时,会对其生长产生不利的影响。随着浸提液浓度的升高,可溶性糖和可溶性蛋白含量呈先上升后下降的趋势,而脯氨酸含量则持续增加。与CK相比,T1的MDA含量、细胞膜损伤率和H₂O含量差异不显著,而T3、T4则显著升高。茶树凋落叶浸提液对抗氧化酶活性及其基因表达有不同的影响,T1的过氧化物酶(POD)与抗坏血酸氧化物酶(APX)活性最高,T2的过氧化氢酶(CAT)活性最高,而T3、T4的4种抗氧化酶活性均显著低于CK。T1的Pod、Cat、Apx基因表达量最高,而T4则抑制了抗氧化酶基因的表达。此外,POD活性与其基因表达量呈显著正相关,而超氧化物歧化酶(SOD)、CAT和APX活性与其基因表达量的相关性不显著。不同浓度的茶树凋落叶浸提液对于菘蓝次生代谢物质积累的影响存在显著差异,低浓度茶树凋落叶浸提液对菘蓝生长、靛蓝和靛玉红含量积累有促进作用,而高浓度茶树凋落叶浸提液对总黄酮含量积累有一定的促进作用。本研究结果可为幼龄茶园中茶树-菘蓝复合种植提供理论参考。     

茶树CsSNAT基因的克隆与表达分析

为明确茶树SNAT基因的序列特征和表达特点,在茶树转录组测序的基础上以茶树(Camellia sinensis)品种舒茶早为试验材料,通过SMART^TM RACE技术克隆茶树褪黑素合成途径中关键限速酶5-羟色胺-N-乙酰转移酶CsSNAT基因的cDNA全长序列,并分析其基因结构和表达模式。结果表明,CsSNAT基因序列全长1 014 bp,其中包含742 bp的完整开放阅读框(ORF),编码247个氨基酸,预测等电点7.64,蛋白分子量27.36 kDa。氨基酸序列比对显示,CsSNAT蛋白与其他高等植物的SNAT蛋白具有较高同源性,与葡萄 VvSNAT(CBI31163)同源性最高,为66.19%。诱导蛋白最佳条件为温度28℃,异丙基-β-D-硫代半乳糖苷(IPTG)浓度0.5 mg·L^-1,诱导时间6 h,在上清液中可获得大量分子量为66 kDa的可溶性融合蛋白。实时定量 PCR 分析表明,CsSNAT在褪黑素处理6 h后表达量最高,为对照的3倍;茶尺蠖取食6 h后,CsSNAT表达显著上调。不同激素处理结果显示,CsSNAT受脱落酸(ABA)、茉莉酸甲酯(MeJA)和水杨酸(SA)诱导表达。本研究结果为5-羟色胺-N-乙酰转移酶功能研究奠定了一定的基础。