Ultrastructure of lycopene containing chromoplasts in fruits ofAglaonema commutatum schott (Araceae)

Summary The ripening process in fruits ofA. commutatum is characterized by clearly distinguishable developmental stages of their pericarp plastids. With respect to predominant pigments and ultrastructural features the following scheme is proposed: 1. The green stage with a tendency to thylakoid degeneration and plastoglobule formation leads to 2. the yellow stage. An increasing number of globules, mostly being membrane associated, are converted to tubules. In this stage, the main pigments are -carotene and cryptoxanthine. The development of membraneous invaginations from the inner plastid envelope leads to 3. the red stage. Concomitantly with lycopene synthesis and incorporation, these envelope-derived membranes expand and become electron dense (after KMnO₄ treatment), but maintain their triple-layered structure. Chromoplasts of deep red coloured fruits (1,400 g lycopene g^–1 dry wt) contain lycopene crystals within the lumina of membraneous sacs which are also derived from the inner envelope membrane. The molar ratio between the three main pigments -carotene, cryptoxanthine, and lycopene is about 1110 in this final state. GA/OsO₄ fixation is unable to stabilize the lycopenic structures (membranes as well as crystals).     

Genetic relationships of Aglaonema species and cultivars inferred from AFLP markers

BACKGROUND AND AIMS: Aglaonema is an important ornamental foliage plant genus, but genetic relationships among its species and cultivars have not been reported. This study analysed genetic relatedness of 54 cultivars derived from nine species using amplified fragment length polymorphism (AFLP) markers. METHODS: Initially, 48 EcoRI + 2/MseI + 3 primer set combinations were screened, from which six primer sets that showed clear scoreable and highly polymorphic fragments were selected and used for AFLP reactions. AFLP fragments were scored and entered into a binary data matrix as discrete variables. Jaccard's coefficient of similarity was calculated for all pair-wise comparisons among the 54 cultivars, and a dendrogram was constructed by the unweighted pair-group method using the arithmetic average (UPGMA). KEY RESULTS: The number of AFLP fragments generated per primer set ranged from 59 to 112 with fragment sizes varying from 50 to 565 bp. A total of 449 AFLP fragments was detected, of which 314 were polymorphic (70 %). All cultivars were clearly differentiated by their AFLP fingerprints. The 54 cultivars were divided into seven clusters; cultivars within each cluster generally share similar morphological characteristics. Cluster I contains 35 cultivars, most of them are interspecific hybrids developed mainly from A. commutatum, A. crispum or A. nitidum. However, Jaccard's similarity coefficients among these hybrids are 0.84 or higher, suggesting that these popular hybrid cultivars are genetically much closer than previously thought. This genetic similarity may imply that A. nitidum and A. crispum are likely progenitors of A. commutatum. CONCLUSIONS: Results of this study demonstrate the efficiency and ease of using AFLP markers for investigating genetic relationships of ornamental foliage plants, a group usually propagated vegetatively. The AFLP markers developed will help future Aglaonema cultivar identification, germplasm conservation and new cultivar development.     

Anodic asymmetry of leaves and flowers and its relationship to phyllotaxis

BACKGROUND AND AIMS: New approaches are needed to evaluate the various hypotheses of phyllotaxis, and an examination of anodic leaf asymmetry may be one such approach. METHODS: Data were collected on the direction of midrib curvature and leaf coil in Syngonium podophyllum, the location of floral buds in Acalypha virginica, the position of secondary leaves of Croton variegatus 'Banana' and the relative size of half-lamina in Aglaonema crispum and Calathea ornata. KEY RESULTS: All five features were exclusively anodic with respect to the direction of the genetic spiral regardless of whether the spiral was clockwise or counterclockwise. CONCLUSIONS: Any phyllotactic mechanism must include some asymmetric component which cannot be explained by the prevalent hypotheses of contact parastichies, inhibitory fields, available space, pressure waves and auxin transport. The most favourable hypothesis is the primary vasculature explanation as it includes an asymmetric feature.     

广东万年青的细胞遗传学研究

采用常规压片法和去壁低渗法,以生长于广西凭祥和广东深圳的广东万年青（Aglaonema modestumSchott ex Engl.）为材料,对二者的体细胞染色体、花粉母细胞减数分裂染色体配对行为和花粉发育过程进行了观察。结果表明：（1）野生植株为二倍体2n=40,栽培植株为三倍体2n=60;（2）野生种的小孢子母细胞减数分裂前期I终变期均为二价联会,栽培种偶见三价联会;（3）中期I,野生种为20个二价体排列在赤道板上,未见单价体,栽培种的20个二价体排列于赤道板上,20个单价体随机分布于两极,证实其为三倍体;（4）后期I,野生种二价体分离,出现单染色单体桥和断片,几率为10%,栽培种几率为3%,还存在落后染色体,部分不能进入两极的落后染色体和染色体断片在末期I形成微核;（5）四分体时期,野生种未观察到异常孢子,栽培种出现大量败育的四分体或多分体;（6）小孢子进入正常的发育分化,通过两次有丝分裂形成三细胞型花粉。野生种成熟花粉败育率为2.18%,栽培种为88.29%;（7）野生种正常结实,栽培种果实中未发现种子,为高度不育。     

不同光质与光周期对粗肋草生长、叶片色素和颜色的影响

为改良粗肋草叶色和优化粗肋草设施栽培体系,该研究以粗肋草品种‘吉利红''的水培苗为材料,设置6种光质(白光、R:B=1:1、R:B=1:2、R:B=2:1、R:B=1:3、R:B=3:1,其中R、B分别代表红光、蓝光)和2种光周期(8、12 h·d^-1)交叉培养,测定粗肋草的生长量、生物量、土壤和作物分析仪器开发(SPAD)值、花色素苷含量和叶片颜色参数(色相值a^*、色相值b^*、明度值L^*、色调角h^*),研究粗肋草对红蓝光质和光周期互作的响应。结果表明:(1)12 h·d^-1光周期更有利于粗肋草生物量的积累,其中LP11(R:B=1:3×12 h·d^-1)处理的粗肋草苗木干重、鲜重均为最高,最有利于植物生长及生物量积累; 其次是LP5(R:B=1:3×8 h·d^-1)处理。(2)相同光质条件下,8 h·d^-1光周期处理的粗肋草叶片SPAD值比12 h·d^-1光周期处理高,12 h·d^-1光周期处理的粗肋草叶片花色素苷含量高于8 h·d^-1光周期的处理,LP11处理叶片SPAD值最低,花色素苷含量最高。12 h·d^-1光周期培养的粗肋草叶片颜色参数a^*、b^*值比8 h·d^-1光周期高,h^*值比8 h·d^-1光周期低。(3)主成分分析结果表明,LP11处理在促进粗肋草生长及叶色改良方面效果最好。综上认为,12 h·d^-1光周期更有利于粗肋草的生长和叶片颜色变化,其中LP11处理为最佳光质和光周期组合。     

Purification and characterization of a β-galactosidase from Sclerotinia sclerotiorum

The DNA coding for the eight structural genes and uncI of the sodium dependent ATPase of Propionigenium modestum has been cloned and sequenced. Based on sequence homology, the genes were determined to appear in the order uncBEFHAGDC as in several other bacterial species. Minicell experiments revealed that plasmids containing the P. modestum DNA expressed those ATPase polypeptides in Escherichia coli. These were very similar in molecular mass to those obtained from the purified ATPase of P. modestum. No membrane-bound ATPase activity was observed in E. coli unc deletion strains containing the P. modestum ATPase genes. Amino acid alignments which were done with the Fo subunits revealed only a few conservative changes in the highly conserved regions of the polypeptides.