C3与C4植物的环境调控

环境条件决定着不同光合类型植物的地理分布范围和区域 ,一般来说 ,C4 植物分布于高温、强光的环境而 C3植物分布于阴凉、湿润的环境 ,且 C4 比 C3植物光合速率高。但环境条件影响着不同光合类型植物的光合潜能的发挥 ,C4 植物在高温、强光、干旱条件下所表现出来的优势在其它环境条件下未必就显现出来。环境条件甚至可以引起 C3、C4 光合途径间的相互转化 ,这使得目前几种鉴别植物光合类型的方法出现不一致的结果。因此 ,在判断植物的光合类型时 ,要注意多种手段的综合利用 ,同时注意植物所处环境条件的影响。     

Pyrones from the bark of Garcinia conrauana: Conrauanalactone,a novel C20 derived α-pyrone

Conrauanalactone has been isolated from the bark of Garcinia conrauana Engl. (Guttiferae) and identified, on the basis of spectral and chemical evidence, as 4-hydroxy-6-pentadecyl- 2-pyrone. Minor constituents of the bark have been identified as 5,7-dihydroxychromone and eriodictyol.     

C3、C4和CAM途径的生态学意义

本文通过C_3,C_4和CAM植物在不同环境中的分布,从3个方面阐述了这3种碳同化途径在利用环境资源时的生态学意义——资源分隔: 1.光合途径的空间分异:(1)不同光合类型植物的气候带(水平和垂直带)和地理区域分布;(2)不同光合类型植物在微环境中的分布。 2.光合途径的时间分异。 3.光合途径在资源分隔中的重叠。     

中国东北草原植物中的C3和C4光合作用途径

以光合作用关键羧化酶ＰＥＰＣ和ＲｕＢＰＣ活性化,并且参照叶片ＣＯ补偿浓度,δ＾１３Ｃ值和叶片解剖结构特点来鉴定东北草原区２３３种植物的Ｃ３,或Ｃ４光全作用途径,这些植物隶属于１４４属７３科,其中１３７种为首次鉴定。８９种具有Ｃ４光合作用途径,隶属于５５属１７科;１４４种人有Ｃ３光俣作用途径;隶属于９４属２８在多数Ｃ４种分布在禾本科、莎草科、苋科和藜科。苋属、地肤属、狗昌属和虎尾草属中的均为Ｃ４植物     

C3和C4植物叶片对光氧化响应的日变化

田间生长的C3植物花生和C4植物玉米分别于晴天上午9：00、中午12：00、下午15：00取样。中午12：00花生叶片的Fv／Fm较早上9：见下降16％,出现了光抑制现象,玉米叶片的Fv／Fm则未下降。不同时间取样的花生和玉米叶片经甲基紫精（MV） 强光的人为光氧化处理,叶绿素和类胡萝卜素出现不同程度的氧化降解,中午12：00降解幅度最大,15时降幅最小。植物叶片的抗氧化能力与其SOD活性相关,而与PEPCase的活性没有明显的相关性。光氧化处理后,花生和玉米的叶绿素荧光参数FV／Fm、qp、pSII都下降,花生在12：00的降幅最小,玉米的降幅最大。光氧化引起花生的qN和热耗散系数（KD）上升,玉米则都下降．结果显示C3植物花生和C4植物玉米对光氧化的响应可能存在不同的机制。     

The reaction of [η:C5H4-(CH2)n-C6H5]2MCl2 complexes (n=1-5; M=Zr, Hf) with EtLi

The reaction of metallocene complexes of the type [η⁵:C₅H₄-(CH₂)_n-C₆H₅]₂MCl₂ (n=1-5; M=Zr, Hf) with EtLi gives the mono nuclear ethyl derivatives [η⁵:C₅H₄-(CH₂)_n-C₆H₅]₂M(Et)Cl and the metallacycles [η⁵:C₅H₄-(CH₂)_n-C₆H₅][η⁵:C₅H₄-(CH₂)_n-η¹:C₆H₄]MEt. A large excess of EtLi affords the dinuclear species [η⁵:C₅H₄-(CH₂)_n-η⁶:C₆H₅]₂M₂Cl₂ (n=2-5). All types of complexes can be activated with methylalumoxane (MAO) and then be used for catalytic polymerization of ethylene.     

1,3-Bis(α-aminoisopropyl)benzene, meta-C6H4(CMe2NH2)2: An N,N-bridging and N,C,N-cyclometalating ligand

Saponification of the bis(carbamic acid ester) 1,3-C₆H₄(CMe₂NHCO₂Me)₂ (1), made by the addition of methanol to commercial 1,3-C₆H₄(CMe₂NCO)₂, yielded the meta-phenylene-based bis(tertiary carbinamine) 1,3-C₆H₄(CMe₂NH₂)₂ (2). Dinuclear [{(η⁴-1,5-C₈H₁₂)RhCl}₂{μ-1,3-C₆H₄(CMe₂NH₂)₂}] (3) resulted from the action of 2 on [{(η⁴-1,5-C₈H₁₂)Rh(μ-Cl)}₂] in toluene. Combination of 2 with PdCl₂ or K₂[PdCl₄] gave the dipalladium macrocycle trans,trans-[{μ-1,3-C₆H₄(CMe₂NH₂)₂}₂(PdCl₂)₂] (4) along with cyclometalated [{2,6-C₆H₃(CMe₂NH₂)₂-κN,κC¹,κN′}PdCl] (5). Substitution of PEt₃ for the labile chlorido ligand of 5 afforded [{2,6-C₆H₃(CMe₂NH₂)₂-κN,κC¹, κN′}Pd(PEt₃)]Cl (6). The crystal structures of the following compounds were determined: bis(carbamic acid ester) 1, ligand 2 as its bis(trifluoroacetate) salt [1,3-C₆H₄(CMe₂NH₃)₂](O₂CCF₃)₂, 2 · (HAc_f)₂, complexes 3 and 6, as well as 1,3-C₆H₄(CMe₂OH)₂ (the diol analogue of 2).     

The molecular structure of (20R)-20-phenyl-5-pregnene-3β,20-diol,an inhibitor of cholesterol conversion to pregnenolone

The crystal and molecular structure of (20R)-20-phenyl-5-pregnene-3β, 20-diol hemihydrate has been determined by X-ray analysis in order to establish the configuration and conformation at C(20). Interest in this compound was stimulated by its high affinity inhibitory binding to cytochrome P-450_SCC, the enzyme which catalyzes the biosynthesis of pregnenolone(3β-hydroxy-5-pregnen-20-one) from cholesterol. The results of the analysis suggest a possible conformation for the cholesterol side chain in the enzyme complex.     

开放式空气CO2浓度增高条件下C3作物(水稻)与C4杂草(稗草)的竞争关系

通过田间试验,研究了FACE(开放式空气CO₂浓度升高)条件下C₃作物水稻(Oryza sativa)和C₄杂草稗草(Echinochloa crusgalli)的生长和竞争关系.结果表明,FACE条件下C₃植物水稻生物量和产量增加,叶片数增加,分蘖数增加,叶面积系数(LAI)增大;而C₄植物稗草相反.FACE条件下水稻和稗草叶面积均减少,而净同化率(NAR)均增加.FACE条件下水稻稗草比例为1:1时,水稻与稗草的生物量比率、产量比率、LAI比率、茎蘖比率和NAR比率均增加,水稻稗草的竞争关系发生变化,水稻(C₃植物)竞争能力增加,稗草(C₄植物)竞争能力下降.     

Chalcogenide-capped triruthenium clusters: X-ray structures of [Ru3(CO)6(μ3-CO){P(C4H3S)3}(μ-dppm)(μ3-O)] and [(μ-H)2Ru3(CO)6{P(C4H3S)3}(μ-dppm)(μ3-S)]

Treatment of [Ru₃(CO)₉{P(C₄H₃S)₃}(μ-dppm)] (1) [dppm = bis(diphenylphosphino)methane] with molecular oxygen in benzene at 60 °C affords oxo-capped [Ru₃(CO)₆(μ₃-CO){P(C₄H₃S)₃}(μ-dppm)(μ₃-O)] (2), while with elemental sulfur and selenium related chalcogenide-capped clusters [Ru₃(CO)₆(μ₃-CO){P(C₄H₃S)₃}(μ-dppm)(μ₃-E)] (3, E = S; 5, E = Se) and bis(chalcogenide) clusters [Ru₃(CO)₆{P(C₄H₃S)₃}(μ-dppm)(μ₃-E)₂] (4, E = S; 6, E = Se) result. Reaction of 1 with H₂S in refluxing THF affords the previously reported [(μ-H)₂Ru₃(CO)₇(μ-dppm)(μ₃-S)] (7) together with the new sulfido-capped dihydride [(μ-H)₂Ru₃(CO)₆{P(C₄H₃S)₃}(μ-dppm)(μ₃-S)] (8). All new compounds have been characterized by spectroscopic data, and 2 and 8 by single-crystal X-ray diffraction analyses. Oxo-capped 2 consists of a triangular ruthenium framework capped on opposite sides by oxo and carbonyl groups, while 8 consists of a ruthenium triangle by a capping sulfido ligand and two inequivalent bridging hydride ligands.     

Biosynthesis of α-spinasterol from (2- 14C (4R)-4-3H1) mevalonic acid by Spinacea oleracea and Medicago sativa

Leaves of Spinacea oleracea and Medicago sativa were incubated with (2-¹⁴C, (4R)-4³H₁ mevalonic acid and the sterols isolated. Cycloartenol had a ³H: ¹⁴C atomic ratio of 6:6 whilst oxidation to cycloartenone resulted in a ratio of 5:6 showing that tritium was present in the 3α-position and that the cycloartenol was symmetrically labelled. Separation of the 4-demethyl sterols gave α-spinasterol and a mixture of stigmast-7-enol and 24-methylcholest-7-enol, which had ³H: ¹⁴C atomic ratios of 3:5. Ozonolysis of α-spinastery] acetate gave the terminal side chain fragment as 2-ethyl-3-methyl butanoic acid. The acid contained ¹⁴C but no tritium thus showing that the C-24 hydrogen of cycloartenol is lost during the alkylation reactions leading to the C-24 ethyl group of α-spinasterol.     

Maintenance of lower proportions of (n − 6) eicosanoid precursors in phospholipids of human plasma in response to added dietary (n − 3) fatty acids

Competition between the (n ? 3) and (n ? 6) types of highly unsaturated fatty acids can diminish the abundance of (n ? 6) eicosanoid precursors in a tissue, which in turn can diminish the intensity of tissue responses that are mediated by (n ? 6) eicosanoids. The mixture of 20- and 22-carbon highly unsaturated fatty acids maintained in the phospholipids of human plasma is related to the dietary intake of 18:2 (n ? 6) and 18:3 (n ?3) by empirical hyperbolic equations in a manner very similar to the relationship reported for laboratory rats (Lands, W.E.M., Morris, A. and Libelt, B. (1990) Lipids 25, 505–516). Analytical results from volunteers ingesting self-selected diets showed an inter-individual variance for the proportion of (n ? 6) eicosanoid precursors in the fatty acids of plasma phospholipids of about 5%, but the variance among multiple samples taken from the same individual throughout the day was less (about 3%), closer to the experimental variance of the analytical procedure (about 1%). The reproducibility of the results makes it likely that analysis of fatty-acid composition of plasma lipids from individuals will prove useful in estimating the diet-related tendency for severe thrombotic, arthritic of other disorders that are mediated by (n ? 6) eicosanoids. Additional constants and terms were included in the equations to account for the effects of 20- and 22-carbon highly unsaturated (n ? 3) fatty acids in the diet. A lower constant for the 20- and 22-carbon (n ? 3) fatty acids compared to that for the 18-carbon (n ? 3) fatty acid in decreasing the ability of dietary 18:2 (n ? 6) to maintain 20:4 (n ? 6) in tissue lipids confirmed the greater competitive effectiveness of the more highly unsaturated n ? 3 fatty acids in the elongation/ desaturation process. Also, a lower constant for direct incorporation of 20-carbon fatty acids of the n ? 6 vs. the n ? 3 type indicated a greater competitive effectiveness of 20:4 (n ? 6) relative to 20:5 (n ? 3) in reesterification after release from tissue lipids. The equations may be used in reverse to estimate the dietary intakes of the (n ? 3) and (n ? 6) fatty acids by using the composition of the fatty acids that had been maintained in plasma lipids.     

N-acetylglucosamine kinase, HXK1 contributes to white–opaque morphological transition in Candida albicans

Morphological transition (yeast-hyphal and white–opaque) is an important biological process in the life cycle of pathogenic yeast, Candida albicans and is a major determinant of virulence. Earlier reports show that the amino sugar, N-acetylglucosamine (GlcNAc) induces white to opaque switching in this pathogen. We report here a new contributor to this switching phenomenon, namely N-acetylglucosamine kinase or HXK1, the first enzyme of the GlcNAc catabolic cascade. Microarray profile analysis of wild type vs. hxk1 mutant cells grown under switching inducing condition showed upregulation of opaque specific and cell wall specific genes along genes involved in the oxidative metabolism. Further, our qRT-PCR and immunoblot analysis revealed that the expression levels of Wor1, a master regulator of the white–opaque switching phenomenon remained unaltered during this HXK1 mediated transition. Thus the derepression of opaque specific gene expression observed in hxk1 mutant could be uncoupled to the expression of WOR1. Moreover, this regulation via HXK1 is independent of Ras1, a major regulator of morphogenetic transition and probably independent of MTL locus too. These results extend our understanding of multifarious roles of metabolic enzymes like Hxk1 and suggest an adaptive mechanism during host–pathogen interactions.     

中国南亚热带和北温带地区禾本科C3与C4草本植物花果期差异研究

为揭示不同地区禾本科C₃与C₄植物花果期受气候因子的影响,以广东省和内蒙古自治区分别代表南亚热带和北温带地区,从植物志中分别获得两地395和265种禾本科草本植物的3个花果期特征(始花期、末花果期和生殖期长),比较开花物候的差异,并通过一般线性模型探究其与气候因子(年均温与年均降水量)的相关性。结果表明,南亚热带与北温带地区C₃植物的始花期均比C₄植物早。两地C₄共有种在南亚热带地区具有更早的始花期、更晚的末花果期和更长的生殖期,而C₃共有种的末花果期在两地无显著差异,但在南亚热带地区始花期更早,生殖期更长。随年均温升高,北温带地区禾本科植物的始花期提前,而南亚热带地区则延后;随年均降水量升高,两地禾本科植物始花期与末花果期均延迟;禾本科植物生殖期长与年均温和年均降水量均不存在相关性。跨地区分析表明,末花果期、生殖期长与年均温和年均降水量均正相关,而与始花期不相关。禾本科C₃植物比C₄植物对地区间气候差异响应更敏...     

C3和C4植物寄主对华北地区棉铃虫越冬代和第一代的影响

确定华北越冬代棉铃虫虫源及其对第一代棉铃虫种群的影响是制定棉铃虫防治策略的基础。以越冬代棉铃虫蛾翅的稳定同位素δ¹³C为天然标记直接判定这些成虫的幼虫期寄主类型,并将雌虫接到春小麦植株上,调查其产卵、孵化、幼虫发育至化蛹、羽化等特征。结果表明,越冬代来自C₃植物(主要为棉花)的成虫个体数量占全部越冬羽化种群的53.1%,所产生的下一代老熟幼虫也较C₄来源的多(55.1%);雌蛾受精率都比较高;卵孵化率较高(52.9%>41.6%);幼虫发育在低龄阶段较比后者快,存活率低,但在高龄幼虫阶段相对后者慢,存活率高;与C₄植物(主要玉米)的来源个体后代的幼虫发育总历期接近,总存活率也相近。显示寄主植物小麦提供的营养条件在第一代棉铃虫的幼虫发育中具有决定性意义,即小麦只在特定阶段才适合幼虫的发育;而且不论是C₃还是C₄寄主来源的越冬代棉铃虫已经适应了这一限制。有效地评价了玉米和棉花等寄主植物对华北地区越冬代和次年第一代棉铃虫的影响,对于分析越冬代棉铃虫的虫源性质和第一代棉铃虫的防治及Bt抗性的治理有重要参考价值。     

Oxidation of [Ir(η-C5Me5)(C8H4S8)] and crystal structures of [IrI(η-C5Me5)(C8H4S8)](I3) and [IrI(η-C5Me5)(C8H4S8)](I3)1/2(I7)1/2

[Ir(η⁵-C₅Me₅)(C₈H₄S₈)] (1) [ = 2-{(4,5-ethylenedithio)-1,3-dithiole-2-ylidene}-1,3-dithiole-4,5-dithionate(2−)] was reacted with iodine in dichloromethane to afford one-electron- and two-electron-oxidized species [IrI(η⁵-C₅Me₅)(C₈H₄S₈)] (2), [IrI(η⁵-C₅Me₅)(C₈H₄S₈)](I₃) (3) and [IrI(η⁵-C₅Me₅)(C₈H₄S₈)](I₅) (4). The oxidized species exhibit electrical conductivities of (1.1-5.0) × 10⁻⁶ S cm⁻¹ measured for compacted pellets at room temperature. The X-ray crystal structures of the two-electron-oxidized complexes 3 and 4 revealed the Ir-I bonds for both of them and the presence of for 3 and ions for 4 as the counter anions. They have many S-S and S-I non-bonding contacts to form two-dimensional molecular interaction sheets in the solid state.     

A cyclic osmastannyl complex, Os(κ(Sn,P)-SnMe2C6H4PPh2)(κ-S2CNMe2)(CO)(PPh3) derived from the osmastannol complex, Os(SnMe2OH)(κ-S2CNMe2)(CO)(PPh3)2

Treatment of the six-coordinate trimethylstannyl complex, Os(SnMe₃)(κ²-S₂CNMe₂)(CO)(PPh₃)₂ (1) with SnMe₂Cl₂ produces Os(SnMe₂Cl)(κ²-S₂CNMe₂)(CO)(PPh₃)₂ (2), which in turn reacts readily with hydroxide ion to give, Os(SnMe₂OH)(κ²-S₂CNMe₂)(CO)(PPh₃)₂ (3). The osmastannol complex 3 undergoes a reaction with 2 equivalents of ^tBuLi, in which one of the phenyl rings of a triphenylphosphine ligand is “ortho-stannylated”, without cleavage of the Os-Sn bond, to give the cyclic complex, Os(κ²(Sn,P)-SnMe₂C₆H₄PPh₂)(κ²-S₂CNMe₂)(CO)(PPh₃) (4). This novel cyclic complex is selectively functionalised at the tin atom by reaction with SnMe₂Cl₂ which exchanges one methyl group for chloride giving the diastereomeric mixture, Os(κ²(Sn,P)-SnMeClC₆H₄PPh₂)(κ²-S₂CNMe₂)(CO)(PPh₃) (5a/5b). Crystal structure determination reveals that both diastereomers occur in the unit cell. The mixture, 5a/5b, undergoes reaction with hydroxide ion to give the diastereomeric osmastannol complexes, Os(κ²(Sn,P)-SnMeOHC₆H₄PPh₂)(κ²-S₂CNMe₂)(CO)(PPh₃) (6a/6b) and with sodium borohydride to give the corresponding tin-hydride mixture, Os(κ²(Sn,P)-SnMeHC₆H₄PPh₂)(κ²-S₂CNMe₂)(CO)(PPh₃) (7a/7b). Crystal structure determinations for 2, 4, and 5a/5b have been obtained.     

D and D Nuclear magnetic resonance of new silver(I) complexes with achiral and chiral bases as ligands: Crystal structure of [Ag{(S)-(6-CH3)C5H3N-CHN-C*H(α-CH3)C6H5}(PPh3)2](O3SCF3)

Treatment of equimolar amounts of substituted aniline or amine with substituted benzaldehyde leads to the corresponding achiral or chiral Schiff bases (L). The reaction of the bases with [Ag(O₃SCF₃)(PPh₃)] leads to the preparation of three or four coordinated cationic complexes, [Ag(k¹-L)(PPh₃)_n]⁺ (n = 1 or 2) which have been characterized by IR, ¹D and ²D NMR spectroscopy. The crystal structure of [Ag{(S)-(6-CH₃)C₅H₃N-CHN-C*H(α-CH₃)C₆H₅}(PPh₃)₂](O₃SCF₃) is reported.     

Hydrido-derivatives of [Ir4(CO)10(diphosphine)]: X-ray analyses of [Ir4H(CO)9(μ-Ph2PH(CH3)PPh2)] and [Ir4 H(CO)9(μ-Ph2P(CH2)nPPh2)] (n = 2, 3)

Some novel hydrido-anions of general formula [Ir₄H(CO)₉(μ-L-L)]⁻ (L-L = Ph₂PCH(CH₃)PPh₂, Ph₂P(CH₂)₂PPh₂, Ph₂P(CH₂)₃PPh₂ and Ph₂AsCH₂AsPh₂) have been obtained by the reaction of [Ir₄(CO)₁₀(μ-L-L)] with the base 1,8-diazabicyclo[5.4.0]undec-7-ene in wet dichloromethane. According to IR and ¹H, ³¹P and ¹³C NMR data at low temperature, these anionic derivatives display a single conformation in solution: three edge-bridging COs around the triangular basal face and both the hydride and the bidentate ligands located in axial positions relative to this face. The structures of four compounds were established by X-ray diffraction studies, which confirmed the configuration proposed on the basis of spectroscopic data.