基于叶绿体基因组数据的芸香科属间系统发育初步分析（专题约稿）

该研究在人工控制水分条件下,设置3个干旱胁迫处理,选用3个主栽油菜品种‘陇油10号’、‘陇油2号’、‘青杂5号’幼苗进行盆栽试验,测定干旱胁迫条件下叶片相对含水量、叶绿素含量、光合气体交换参数及叶绿素荧光参数等指标,考察各指标在干旱胁迫过程中的变化特征,并通过主成分分析(PCA)和隶属函数法评价品种的抗旱性及其主要响应因子,以揭示西北地区油菜幼苗响应干旱胁迫的光合调控机制。结果表明：(1)各品种油菜幼苗的叶片相对含水量(RWC)均随干旱胁迫程度的递增而逐渐降低,最大水分亏缺(WSD)却逐渐上升。(2)各品种油菜幼苗叶片的叶绿素a含量、叶绿素总含量随着干旱胁迫程度的递增而先增加后递减,且同一种幼苗在不同处理间差异显著。(3)各品种油菜幼苗叶片的净光合速率(P_n)、水分利用效率(WUE)、单株生物量、气孔导度(G_s)、胞间CO₂浓度(C_i)均在受到干旱胁迫时迅速降低,且同一品种幼苗在不同处理间差异显著,而其叶片蒸腾速率(T_r)在干旱胁迫下无显著变化。(4)各品种油菜幼苗叶片光化学猝灭系数(qP)和非光化学猝灭系数(NPQ)随着干旱胁迫程度的递增先增加后递减,最大光化学效率(F_v/F_m)和电子传递速率(ETR)在受到干旱胁迫时迅速降低,且同一品种幼苗在不同处理间差异显著。(5)主成分分析结果表明,在油菜幼苗受到干旱胁迫时RWC、C_i、G_s、P_n、WUE、叶绿素总含量、叶绿素a含量和NPQ起主要调控作用;隶属函数法综合评价表明,3个品种油菜幼苗耐旱能力由高到低依次为‘陇油10号’＞‘陇油2号’＞‘青杂5号’。     

干旱胁迫对燕麦生长及叶片光系统Ⅱ活性的影响

以‘燕科2号’燕麦品种为试验材料,采用盆栽控水的方式分别设置正常供水(75%田间持水量)、中度干旱胁迫(60%田间持水量)、重度干旱胁迫(45%田间持水量)3个水分处理,利用叶绿素荧光技术研究了不同水分梯度下燕麦生长和叶片光反应系统Ⅱ(PSⅡ)功能的变化,探讨干旱胁迫对燕麦叶片光合性能的影响。结果表明：(1)干旱胁迫导致燕麦株高变矮,叶片数、主茎数、穗数减少,叶片失绿发黄及籽粒产量显著下降。(2)与正常供水相比,重度干旱胁迫下燕麦叶片最大光化学效率(F_v/F_m)和光合性能指数(PI_ABS)显著降低。(3)重度干旱胁迫导致燕麦叶片单位反应中心吸收的光能(ABS/RC)和单位反应中心耗散掉的能量(DI₀/RC)明显下降,单位反应中心用于电子传递的能量(ET₀/RC)和单位反应中心捕获的光能(TR₀/RC)明显升高;有活性反应中心的开放程度(Ψ₀)和电子传递链的量子产额(φ_E0)明显下降、非光化学淬灭最大量子产额(φ_D0)明显升高,V_J、V_K、V_L 3个位点的相对荧光强度明显升高,OJIP曲线初始斜率M_o明显升高。研究发现,燕麦叶片PSⅡ对中度干旱胁迫具有较强的适应能力,而重度干旱胁迫严重伤害其叶片PSⅡ反应中心,导致其反应中心能流分配失衡,电子传递受阻和PSⅡ稳固性减弱,进而影响燕麦光合作用,最终导致燕麦生长受到抑制。     

3种荒漠植物光合及叶绿素荧光对干旱胁迫的响应及抗旱性评价

利用盆栽试验结合人工浇水后自然耗水的方法测定干旱胁迫对梭梭、白刺、沙蒿3种荒漠植物叶片水分、光合及叶绿素荧光参数的影响,探讨各指标在干旱胁迫过程中的变化特征、响应机制及其与土壤水分的定量关系,并用隶属函数法对其进行抗旱性排序。结果表明：(1)3种植物叶片相对含水量(RWC)随干旱胁迫天数增加持续降低,最大水分亏缺(RWD)呈波动式上升趋势。(2)3种植物总叶绿素含量(Chl)和叶绿素a(Chla)、叶绿素b(Chlb)含量,以及梭梭、白刺类胡萝卜素含量均随胁迫天数增加而降低;沙蒿类胡萝卜素随土壤含水率降低逐渐升高。(3)梭梭、白刺、沙蒿叶片净光合速率(P_n)、蒸腾速率(T_r)、水分利用效率(WUE)等主要光合气体交换参数对土壤水分表现出明显的阈值响应,适宜的土壤含水率分别为8.04%～19.33%、4.17%～19.10%、6.48%～17.51%。(4)3种植物 PSⅡ最大光化学效率(Fv/F_m)、实际光化学效率(F_v′/F_m′)及光化学淬灭系数(qP)均随干旱胁迫天数增加和光照强度增大而降低,非光化学淬灭系数(NPQ)则呈逐渐上升趋势;干旱胁迫中后期,梭梭、沙蒿的F_v/F_m及F_v′/F_m′均下降,光合机构光合活性遭到破坏,电子传递受阻,PSⅡ反应中心受损,表现出光抑制,而白刺调节自身PSⅡ反应中心免受伤害的能力较强。(5)隶属函数法综合分析表明,3种植物耐旱能力大小依次为白刺>梭梭>沙蒿。研究发现,3种荒漠植物均可通过调节 PSⅡ反应中心开放程度与活性,对干旱胁迫表现出较强的耐性,胁迫后期植物PSⅡ反应中心关闭或不可逆失活,表现出光抑制。     

秸秆覆盖与施磷对西南冬小麦叶肉导度和CO2同化效率的影响

为探究西南麦区冬小麦旗叶叶肉导度(g_m)与CO₂同化对土壤速效磷缺乏的响应。试验于2020-2022年在四川仁寿试验站进行秸秆覆盖和磷素水平的二因素裂区试验,以秸秆覆盖(SM)和不覆盖(NSM)为主区;三个磷水平0(P0)kg/hm²、75(P75)kg/hm²和120(P120)kg/hm²为裂区,分析小麦旗叶光响应曲线、叶肉导度和CO₂同化对旗叶磷素水平的响应。结果表明:与NSM相比,SM下旗叶比叶重(LMA)、单位面积磷含量(PA)、单位质量磷含量(PM)和净光合速率(P_n)分别提高4.1%、16.9%、12.2%和6.9%,且随着施磷量的增加,旗叶的LMA、PA、PM和P_n呈增加趋势。秸秆覆盖与施磷显著提高旗叶最大净光合速率(P_nmax)和表观量子效率(AQY),增加旗叶的光合潜能。施磷显著提高旗叶光系统II实际光化学效率(ΦPSII),最大羧化效率(V_cmax)、核酮糖-1,5-二磷酸羧化酶(Rubisco)活力、胞间CO₂浓度(C_c)、叶绿体CO₂浓度(C_c)、气孔导度(g_s)和g_m,P75和P120较P0分别提高16.8%-23.8%、27.9%-35.3%、30.9%-61.7%、1.4%-3.6%、4.8%-13.1%、9.0%-10.2%和16.0%-16.9%,P75和P120无显著差异。秸秆覆盖与施磷降低旗叶的气孔限制(L_s)和叶肉限制(L_m),生化限制(L_b)是光合速率的主要限制因子。综上所述,秸秆覆盖配施75kg/hm²磷肥可提高西南冬小麦旗叶磷素含量、光系统II实际光化学效率、叶肉导度和CO₂同化效率,降低气孔限制和叶肉限制,从而提高旗叶净光合速率。     

黄土丘陵区退耕草地群落优势种叶片光合生理对氮磷添加的响应

以黄土丘陵区退耕草地群落典型优势种白羊草、长芒草和达乌里胡枝子为研究对象,测定不同氮磷（主区N：0,50,100 kg N hm^-2 a^-1;副区P：0,40,80 kg P₂O₅ hm^-2 a^-1）添加处理下叶片光合气体交换参数、叶绿素荧光参数、叶片氮磷含量、光合氮利用效率（PNUE）和光合磷利用效率（PPUE）,探究不同优势种光合生理特征对外源氮磷添加的响应特征与物种差异。结果表明：单独氮添加下,3个优势种的净光合速率（P_n）、蒸腾速率、水分利用效率（WUE_i）、气孔限制值（Ls）和光系统Ⅱ（PSⅡ）活性高于或显著高于未施肥处理,白羊草和达乌里胡枝子的PNUE和PPUE以及长芒草的PPUE显著增加。单独磷添加下,仅达乌里胡枝子的P_n、WUE_i、Ls和PNUE相比未施肥处理显著增加。氮磷共同添加下,50 kg N hm^-2 a^-1处理下,施磷后达乌里胡枝子的P_n以及三个优势种的PNUE显著增加,白羊草的PPUE显著降低;100 kg N hm^-2 a^-1处理下,施磷后达乌里胡枝子的P_n和PNUE均显著增加,白羊草PPUE和长芒草的PNUE的仅在40 kg P₂O₅ hm^-2 a^-1处理下显著增加。3个优势种的P_n均与PSⅡ最大光化学效率和叶片氮含量呈显著正相关关系,长芒草和达乌里胡枝子的P_n与PSⅡ潜在活性和叶片磷含量呈显著正相关关系。总体表明,氮磷对黄土丘陵区退耕草地优势种光合生理具有一定的交互作用,物种属性和施肥水平影响其光合生理特征响应程度。     

干旱条件下外源蔗糖对高表达玉米C4型pepc水稻种子萌发的影响

为揭示外源蔗糖参与干旱胁迫下高表达转玉米C₄ 型磷酸烯醇式丙酮酸羧化酶(phosphoenolpyruvate carboxylase, PEPC)基因(C₄ pepc)水稻(简称：PC)种子萌发的生理机制,该研究以 PC及其未转基因野生型受体‘Kitaake’(简称：WT)的种子为材料,研究外施不同浓度蔗糖联合模拟干旱(10% PEG 6000)处理下,其种子发芽参数、总可溶性糖及可溶性蛋白含量、蔗糖非发酵1 (sucrose nonfermenting 1, SNF1)相关蛋白激酶(SNF1 related protein kinase 1s, SnRK1s)基因以及PEPC基因表达等参数的变化。结果表明：(1)PEG 6000模拟干旱处理均显著抑制两材料发芽,但明显促进胚根的生长;外施蔗糖则呈现浓度效应,高浓度蔗糖(>150 mmol·L^-1)进一步加剧了干旱对发芽的抑制效应,而低浓度(<30 mmol·L^-1)则可缓解干旱的抑制,但与WT(<30 mmol·L^-1)相比,促进PC水稻萌发的外施蔗糖浓度(<6 mmol·L^-1)更低,且各处理的发芽表现与其α 淀粉酶活性的动态表现一致。(2)与WT相比,外施3 mmol·L^-1蔗糖联合干旱处理下,显著提高了PC种子的发芽率,且伴随PC内源蔗糖含量、总可溶糖和可溶性蛋白含量显著增加;且外施3 mmol·L^-1蔗糖使PC中内源C₃ pepc基因表达下调,而外源导入C₄ pepc基因表达显著增加。(3)与WT相比,干旱处理下外施3 mmol·L^-1蔗糖,PC的糖信号相关基因SnRKs亚家族基因(包括SnRK1s：OsK1a OsK24 OsK35和SnRK2s:SAPK6)的表达也显著增加。研究发现,外施低浓度蔗糖通过上调PC水稻种子中可溶性糖和可溶性蛋白含量,增强SnRK1s亚家族基因和外源C₄ pepc基因的表达,提高了α 淀粉酶活性,从而缓解了干旱胁迫对PC种子萌发的抑制。     

不同苹果砧穗组合的生长及光合特性

以‘垂丝海棠’（Malus halliana）和‘平邑甜茶’（Malus hupehensis）为基砧,分别嫁接品种‘烟富6号’和‘长富2号’接穗,测定4种砧穗组合的嫁接亲和性、接穗生长量、光合与荧光参数及叶绿素含量（SPAD）,并用主成分分析法综合评价砧穗组合的优劣,探讨不同苹果砧穗组合嫁接苗的生长及光合特性,为西北盐碱地选择适宜的苹果砧木提供理论依据。结果表明：（1）4种砧穗组合中‘垂丝海棠/烟富6号’的上下口粗度比最接近1,嫁接亲和性最好。（2）整个生长期内,以‘垂丝海棠’为基砧的2个组合嫁接苗的生长量、净光合速率（P_n）、最大荧光（F_m）、PSⅡ最大光能转化率（F_v/F_m）均显著大于‘平邑甜茶’为基砧的组合,但其胞间CO₂浓度（C_i）及初始荧光（F₀）显著低于‘平邑甜茶’为基砧的组合;光化学猝灭系数（qP）在4种砧穗组合中无显著差异。（3）在8月份光照强度较高时,‘垂丝海棠/烟富6号’ 嫁接苗的气孔导度（G_s）高于其他砧穗组合;以‘垂丝海棠’为基砧的2个组合嫁接苗叶片的蒸腾速率（T_r）和相对叶绿素含量（SPAD）显著高于‘平邑甜茶’ 基砧组合。（4）根据主成分分析对各项指标进行综合评价,按照4个砧穗组合的综合得分由高到低依次为：‘垂丝海棠/烟富6号’、‘垂丝海棠/长富2号’、‘平邑甜茶/长富2号’、‘平邑甜茶/烟富6号’。研究发现,基砧‘垂丝海棠’的适应性优于‘平邑甜茶’,且‘垂丝海棠/烟富6号’砧穗组合的嫁接亲和性高,长势强,光合能力优,为甘肃中部地区适宜的砧穗组合。     

信号分子水杨酸减缓干旱胁迫对紫御谷光合和膜脂过氧化的副效应

为研究信号分子水杨酸(SA)对干旱胁迫下紫御谷光合和膜脂过氧化的影响,为SA应用于紫御谷抗旱育苗提供理论依据,测定分析了SA处理对干旱胁迫下紫御谷幼苗叶片光合和膜脂过氧化相关指标的变化。结果表明:(1)干旱胁迫破坏了紫御谷叶绿体的膜结构,使基粒数量明显减少,垛叠不明显,排列比较松散,而SA处理能在一定程度上保护叶绿体的膜结构。(2)干旱胁迫降低了紫御谷幼苗叶片的叶绿素b和总叶绿素含量,而SA处理能提高干旱胁迫下紫御谷幼苗叶片的叶绿素a、叶绿素b、总叶绿素和胡萝卜素含量。(3)干旱胁迫降低了叶片的净光合速率、气孔导度、蒸腾速率、光饱和点和暗呼吸速率,增加了叶片的光补偿点、CO₂饱和点、CO₂补偿点和光呼吸速率,而SA处理则增加了紫御谷幼苗叶片的净光合速率、气孔导度、光饱和点和暗呼吸速率,降低了紫御谷幼苗叶片的光补偿点、CO₂饱和点、CO₂补偿点和光呼吸速率。(4)干旱胁迫降低了紫御谷幼苗叶片的F_v/F_m和Φ_PSⅡ,显著增加了叶片的相对电导率和丙二醛含量,而SA处理则增加了幼苗叶片的F_v/F_m和Φ_PSⅡ,降低了叶片的相对电导率和丙二醛含量。表明:信号分子水杨酸能够有效减缓干旱胁迫对紫御谷光合和膜脂过氧化的影响。     

干旱胁迫对玉米苗期叶片光合作用和保护酶的影响

以玉米品种郑单958(抗旱性强)和陕单902(抗旱性弱)为材料,采用盆栽控水试验,设置3个干旱处理(轻度干旱,中度干旱,重度干旱)和正常灌水,研究了干旱胁迫对玉米苗期叶片光合速率、叶绿素荧光以及相关生理指标的影响。结果表明:(1)干旱胁迫下2个品种叶片净光合速率(P_n)和气孔导度(G_s)显著下降,胞间CO₂浓度(C_i)出现了先下降后上升,而气孔限制值(L_s)上升后下降,说明中度干旱胁迫下叶片P_n下降是气孔因素引起的,重度干旱胁迫下P_n降低主要由非气孔因素引起的。(2)随着干旱胁迫的加剧,2个品种叶片光系统Ⅱ(PSⅡ)的实际量子产量(φPSⅡ)、电子传递速率(ETR)和光化学猝灭(qP)一直下降,而非光化学猝灭(qN)上升后下降,说明中度干旱下热耗散仍是植株重要光保护机制,重度干旱时叶片光合电子传递受阻,PSⅡ受到损伤。(3)干旱胁迫下2个品种叶片的超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性先升高后降低,而丙二醛(MDA)含量一直升高,说明干旱胁迫初期对保护系统酶活性升高有诱导作用,重度胁迫下活性氧清除酶的活性下降,导致细胞膜伤害。这些结果暗示,轻度和中度干旱胁迫下2个玉米品种通过减少光捕获、热耗散和酶活性调节协同作用稳定了光合机构功能,是P_n下降的气孔限制因素;而重度干旱胁迫下光系统Ⅱ和抗氧化酶系统损伤,是P_n下降的非气孔限制因素;郑单958的各生理参数比陕单902受旱影响小,干旱胁迫下仍具有较高的光合效率和较强的保护酶活性是郑单958抗旱的主要生理原因。     

外源硅对自毒作用下黄瓜幼苗生长及光合特性的影响

以‘绿博6号’黄瓜幼苗为试材,采用营养液培法研究不同浓度外源硅(0、0.5、1.0、1.5和2.0 mmol/L)对肉桂酸(cinnamic acid,CA)模拟自毒胁迫(3.0 mmol/L CA)下黄瓜幼苗生长、光合参数和叶绿素荧光参数的影响。结果表明：(1)自毒胁迫显著抑制了黄瓜幼苗的生长、根系形态建成和生物量的积累,显著降低了净光合速率(P_n)、蒸腾速率(T_r)、气孔导度(G_s)和叶绿素(Chl a、Chl b和Chl t)含量,并显著降低了叶片中PSⅡ的电子传递速率(ETR)、PSⅡ实际光化学效率［Y_(Ⅱ)］和光化学淬灭系数(qP)。(2)添加适宜浓度外源硅可有效缓解自毒胁迫对黄瓜幼苗生长的影响,并提高其P_n、G_s、T_r和叶绿素含量,在一定程度上维持叶片光合系统的稳定。(3)添加适宜浓度外源硅能使自毒胁迫下黄瓜叶片的F_v/F_m、ETR、Y_(Ⅱ)和qP显著升高,而非光化学淬灭系数(NPQ)则显著下降。研究发现,添加适宜浓度外源硅能提高自毒胁迫下黄瓜幼苗的叶绿素含量、F_v/F_m、ETR、Y_(Ⅱ)和qP,使光合机构趋于稳定,抑制P_n的下降,缓解自毒胁迫对光合系统的损伤,从而增强黄瓜幼苗对自毒胁迫的抗性,并以1.0 mmol/L外源硅处理的效果最佳。     

Spectrofluorimetric method for the determination of large chlorophyll a/b ratios

A practical spectrofluorimetric calibration method at room temperature is described for determining large chlorophyll a/b ratios on direct extracts from plant material of pigments in 80% aqueous acetone, dimethyl sulfoxide, and N,N-dimethylformamide. The method is based on the work of Boardman and Thorne [Boardman NK and Thorne SW (1971) Biochim Biophys Acta 253: 222–231] who used diethyl ether as solvent. We repeated the calibration in diethyl ether and find significantly different parameters for the calibration curve. The range of standards in this work included solutions with chlorophyll a/b ratios of 10–125 in dimethyl sulfoxide, and of 10–220 in the other solvents. Fluorescence emission spectra were found to be a highly sensitive method for assessing chlorophyll purity. We determined the limits of sensitivity for each solvent from the calibration data. The empirically determined slope of the calibration curve was shown to be related to intrinsic properties of the chlorophylls in solution; this allows predictions of the performance of the method in other solvents.     

两种生境条件下6种牧草叶绿素含量及荧光参数的比较

昆仑山前山牧场海拔较高, 策勒绿洲海拔相对较低, 两者生境差异较大。以昆仑山前山牧场和策勒绿洲边缘两种不同生境条件下生长的6种牧草: 冰草(Agropyron cristatum)、无芒雀麦(Bromus inermis)、矮生高羊茅(Festuca elata)、披碱草(Elymus dahuricus )、红豆草(Onobrychis pulchella)及和田大叶(Medicago sativa var. luxurians)为试验材料, 研究了不同生境条件下牧草叶片叶绿素含量及叶绿素荧光动力学参数的变化情况。结果显示: (1)在两种生境条件下, 昆仑山前山牧场生境生长的牧草叶绿素a、叶绿素b、总叶绿素的含量明显较高, 生长在策勒绿洲生境的牧草品种叶绿素a/b值较高; (2)昆仑山前山牧场生境牧草最大荧光、光系统II (PSII)最大光化学效率、PSII潜在活性和单位面积反应中心的数量的值明显高于策勒绿洲生境品种, 而初始荧光、单位反应中心吸收的光能、单位反应中心捕获的能量、单位反应中心耗散的能量、荧光诱导曲线初始斜率值则低于策勒绿洲生境品种。因此, 两种生境下环境因子发生了改变, 对牧草产生综合的胁迫作用; 策勒绿洲生境明显对牧草生长产生了抑制, 策勒绿洲生境牧草的色素含量降低以及PSII的机构遭到损坏, 导致反应中心一部分失活或裂解, 剩余有活性的反应中心的效率增加, 昆仑山生境则相对比较适宜牧草生长; 两种生境不同牧草叶绿素含量和叶绿素荧光参数的变化幅度不同。     

Conversion of chlorophyll b to chlorophyll a precedes magnesium dechelation for protection against necrosis in Arabidopsis

Chlorophyll is a deleterious molecule that generates reactive oxygen species and must be converted to non‐toxic molecules during plant senescence. The degradation pathway of chlorophyll a has been determined; however, that of chlorophyll b is poorly understood, and multiple pathways of chlorophyll b degradation have been proposed. In this study, we found that chlorophyll b is degraded by a single pathway, and elucidated the importance of this pathway in avoiding cell death. In order to determine the chlorophyll degradation pathway, we first examined the substrate specificity of 7‐hydroxymethyl chlorophyll a reductase. 7‐hydroxymethyl chlorophyll a reductase reduces 7‐hydroxymethyl chlorophyll a but not 7‐hydroxymethyl pheophytin a or 7‐hydroxymethyl pheophorbide a. These results indicate that the first step of chlorophyll b degradation is its conversion to 7‐hydroxymethyl chlorophyll a by chlorophyll b reductase, although chlorophyll b reductase has broad substrate specificity. In vitro experiments showed that chlorophyll b reductase converted all of the chlorophyll b in the light‐harvesting chlorophyll a/b protein complex to 7‐hydroxymethyl chlorophyll a, but did not completely convert chlorophyll b in the core antenna complexes. When plants whose core antennae contained chlorophyll b were incubated in the dark, chlorophyll b was not properly degraded, and the accumulation of 7‐hydroxymethyl pheophorbide a and pheophorbide b resulted in cell death. This result indicates that chlorophyll b is not properly degraded when it exists in core antenna complexes. Based on these results, we discuss the importance of the proper degradation of chlorophyll b.     

Accumulation of the NON‐YELLOW COLORING 1 protein of the chlorophyll cycle requires chlorophyll b in Arabidopsis thaliana

Chlorophyll a and chlorophyll b are interconverted in the chlorophyll cycle. The initial step in the conversion of chlorophyll b to chlorophyll a is catalyzed by the chlorophyll b reductases NON‐YELLOW COLORING 1 (NYC1) and NYC1‐like (NOL), which convert chlorophyll b to 7‐hydroxymethyl chlorophyll a. This step is also the first stage in the degradation of the light‐harvesting chlorophyll a/b protein complex (LHC). In this study, we examined the effect of chlorophyll b on the level of NYC1. NYC1 mRNA and NYC1 protein were in low abundance in green leaves, but their levels increased in response to dark‐induced senescence. When the level of chlorophyll b was enhanced by the introduction of a truncated chlorophyllide a oxygenase gene and the leaves were incubated in the dark, the amount of NYC1 was greatly increased compared with that of the wild type; however, the amount of NYC1 mRNA was the same as in the wild type. In contrast, NYC1 did not accumulate in the mutant without chlorophyll b, even though the NYC1 mRNA level was high after incubation in the dark. Quantification of the LHC protein showed no strong correlation between the levels of NYC1 and LHC proteins. However, the level of chlorophyll fluorescence of the dark adapted plant (F_o) was closely related to the accumulation of NYC1, suggesting that the NYC1 level is related to the energetically uncoupled LHC. These results and previous reports on the degradation of chlorophyllide a oxygenase suggest that the a feedforward and feedback network is included in chlorophyll cycle.     

硫对成熟期烤烟叶绿素荧光参数的影响

通通过液培试验,研究了硫浓度(0.01-32 mmol/L)对成熟期烤烟叶片叶绿素含量和叶绿素荧光参数的影响。结果表明,成熟期烤烟叶绿素a和叶绿素b含量随硫浓度的升高而逐渐增加,但各处理差异未达到显著水平。在2-32 mmol/L处理之间,烤烟叶片的有效量子产量（EQY）、最大量子产量（Fv/Fm）、光合电子传递速率（ETR）随硫浓度增加而降低,非光化学猝灭（NPQ）、非光化学过程中的基本量子产量（Fo/Fm）、PSⅡ水裂解端失活程度（Fo/Fv）和PSⅡ反应中心关闭程度（1-qP）随硫浓度增加而升高,2 mmol/L处理的质体醌库（Fv/2）低于4 mmol/L处理外,但其它处理的均随硫浓度升高而降低。0.01 mmol/L处理烤烟叶片的EQY、Fv/Fm和ETR低于2-8 mmol/L处理,但高于16 mmol/L和32 mmol/L处理,其NPQ、Fo/Fm、Fo/Fv和1-qP变化趋势则与之相反;0.01 mmol/L处理的Fv/2低于4 mmol/L处理的,但高于2 mmol/L及8-32 mmol/L处理;低硫处理烤烟EQY、Fv/Fm和ETR的降低可能不是由Fv/2引起的,而是由于1-qP升高引起的。但16 mmol/L和32 mmol/L处理Fv/Fm 、ETR、EQY降低可能是1-qP与 Fv/2共同作用的结果。     

Effects of nickel hyperaccumulation on physiological characteristics of Alyssum murale grown on metal contaminated waste amended soil

A pot experiment was conducted to investigate the effect of nickel concentration on physiological characteristics of Alyssum murale when grown in a soil mixed with sewage sludge (at the rate of 2.8%). Two types of sludge were used: agricultural sewage sludge (S1) and industrial sewage sludge with an increasing nickel concentration (S2, S3, and S4). Results showed that Ni in shoots was higher than Ni in roots. A. murale is able to concentrate up to 12730 mg/kg Ni in leaves. The highest dry matter yield was observed with plants grown with agricultural sewage sludge. An addition of S2 and S3 increased shoot biomass. However, application of S4 reduced 40% shoot dry weight as compared to the control Ni treatment did not affect all chlorophyll fluorescence parameters. The F(v)/F(m) ratio was stable between Ni treatments. Photosynthesis rate (A) increased with agricultural sewage sludge, but remained stable with variable Ni rates from the industrial sludge. The chlorophyll content increased with S1, S2 and S3 but it remains constant with S4 when compared to the control Therefore, high nickel concentration did not affect the function of the photosynthetic machine of A. murale.     

Recent advances in chlorophyll biosynthesis and breakdown in higher plants

Chlorophyll (Chl) has unique and essential roles in photosynthetic light-harvesting and energy transduction, but its biosynthesis, accumulation and degradation is also associated with chloroplast development, photomorphogenesis and chloroplast-nuclear signaling. Biochemical analyses of the enzymatic steps paved the way to the identification of their encoding genes. Thus, important progress has been made in the recent elucidation of almost all genes involved in Chl biosynthesis and breakdown. In addition, analysis of mutants mainly in Arabidopsis, genetically engineered plants and the application of photo-reactive herbicides contributed to the genetic and regulatory characterization of the formation and breakdown of Chl. This review highlights recent progress in Chl metabolism indicating highly regulated pathways from the synthesis of precursors to Chl and its degradation to intermediates, which are not longer photochemically active.     

Green thoughts in a green shade

The author gives an autobiographical sketch of his path to chlorophyll research, and describes some results. The discussion is largely focused on long wavelength forms of chlorophyll and how they might be generated by self-assembly. Dimers or oligomers, (Chl)_n, result from coordination interactions between the central magnesium atom of one macrocycle and nucleophilic side chains of another i.e., keto C=OMg in the case of Chl a. Coordination interactions mediated by a water molecule coordinated to Mg in one macrocycle and to a nucleophilic group in another e.g., MgO(H)HO=C keto, form aggregates with very different structures and properties; where more than one strong nucleophile or hydrogen bonding group is present in the chlorophyll, e.g., the formyl group in Chl b, the acetyl group of Bchl a, or the hydroxyethyl group of Bchl c, they may also participate in direct coordination interactions with Mg as well as hydrogen bonding to water coordinated to Mg. The magnetic resonance properties of Chl a/water aggregates have provided the basis for the special pair concept for the primary electron donor in photosynthesis. Structural information derived from small angle neutron scattering studies on chlorophyll aggregates is now providing an experimental basis for comprehensive models that integrate antenna and photoreaction center chlorophyll functions.This article was written at the invitation of Govindjee. It has been authored by a contractor of the U.S. Government under contract No. W-31-109-ENG-38. Accordingly, the U.S. Government retains a non-exclusive, royalty-free license to publish or reproduce the published form of this contribution, or allow others to do so, for U.S. Government purposes.     

Phosphorescence of protochlorophyll(ide) and chlorophyll(ide) in etiolated and greening bean leaves

The assignment is presented for the principal phosphorescence bands of protochlorophyll(ide), chlorophyllide and chlorophyll in etiolated and greening bean leaves measured at -196°C using a mechanical phosphoroscope. Protochlorophyll(ide) phosophorescence spectra in etiolated leaves consist of three bands with maxima at 870, 920 and 970 nm. Excitation spectra show that the 870 nm band belongs to the short wavelength protochlorophyll(ide), P627. The latter two bands correspond to the protochlorophyll(ide) forms, P637 and P650. The overall quantum yield for P650 phosphorescence in etiolated leaves is near to that in solutions of monomeric protochlorophyll, indicating a rather high efficiency of the protochlorophyll(ide) triplet state formation in frozen plant material. Short-term (2–20 min) illumination of etiolated leaves at the temperature range from -30 to 20°C leads to the appearance of new phosphorescence bands at about 990–1000 and 940 nm. Judging from excitation and emission spectra, the former band belongs to aggregated chlorophyllide, the latter one, to monomeric chlorophyll or chlorophyllide. This indicates that both monomeric and aggregated pigments are formed at this stage of leaf greening. After preillumination for 1 h at room temperature, chlorophyll phosphorescence predominates. The spectral maximum of this phosphorescence is at 955–960 nm, the lifetime is about 2 ms, and the maximum of the excitation spectrum lies at 668 nm. Further greening leads to a sharp drop of the chlorophyll phosphorescence intensity and to a shift of the phosphorescence maximum to 980 nm, while the phosphorescence lifetime and a maximum of the phosphorescence excitation spectrum remains unaltered. The data suggest that chlorophyll phosphorescence belongs to the short wavelength, newly synthesized chlorophyll, not bound to chloroplast carotenoids. Thus, the phosphorescence measurement can be efficiently used to study newly formed chlorophyll and its precursors in etiolated and greening leaves and to address various problems arising in the analysis of chlorophyll biosynthesis.Abbreviations Pchl protochlorophyll and protochlorophyllide - Chld chlorophyllide - Chl chlorophyll     

植物叶绿素合成、分解代谢及信号调控

叶绿素(Chlorophyll, Chl)合成是决定植物光合效率的重要性状, 是决定作物产量的重要因素。参与植物Chl合成、分解代谢及信号调控的基因数目众多, 其中任何一个基因发生突变都有可能引起Chl含量的变化, 从而表现为各种叶色异常甚至导致植株死亡。自然或人工创造突变体, 对于Chl相关基因的功能分析非常必要。目前, Chl突变体己广泛应用于基础研究和生产实践。文章就该研究领域内的最新研究进展进行了概述。