狗枣猕猴桃果实发育的解剖学观察

对狗枣猕猴桃果实发育进行了显微和超微结构观察。其主要过程可分为：1、早期胚胎发育;多心皮合生子房,通常具16个心室,中轴胎座,中轴上着生大量倒生胚珠,单珠被,具珠被绒毡层,胚囊蓼型,授粉后约2-4h花粉萌发,授粉后约120h花粉管到达胚珠,受精后,初生胚乳核分裂先于合子。胚乳发育为细胞型。2、果壁：果壁可分为果皮,果肉和果心三部分,果皮较薄,由2-3层薄壁细胞组成。外表面光滑无毛,但覆有角质层,气孔下陷,分布于其中,果肉的大部分由薄壁细胞组成,分大,小两种细胞,小细胞含较多淀粉粒,淀粉粒的水解是果实软化的原因之一。果肉薄壁组织细胞还含有叶绿体及两种异细胞,一种异细胞内含物为结晶,普遍存在;另一种含被番红染成红色的絮团状物。果心由维管束和薄壁细胞组成,维管束不发达,3、种子：种皮外表面呈蜂窝状,种皮较硬,由两层细胞构成。线性直立胚,胚乳发达,主要贮藏物是蛋白质。     

狗枣猕猴桃的开发与综合利用

狗枣猕猴桃具有药用、观赏、食用等多方面的用途。分布面广、耐寒性强、易繁多益、值得开发利用。     

绞股蓝果实的发育解剖学研究

应用石蜡切片和扫描电镜的方法,观察了绞股蓝果实与种子的发育过程,结果表明:花后12 d左右,绞股蓝合子开始进行第一次分裂,极核分裂在花后6～7 d,核型胚乳在胚的发育中被吸收,胚的发育为茄型,外珠被呈网格状花纹。假果,表面有蜡质,果壁可明显分为3层,内侧细胞后期解体,种子倒三角形,表面瘤状突起。脱落花果的结构表现为珠被萎缩和胚发育受阻。     

火棘属果实发育解剖学研究

火棘属植物的托附杯呈深杯状,具有５个分离心皮,子房半不位。托附杯发育成肉质果壁,主要藉细胞体积增大,子房壁全部石细胞化,发育成骨质瘦果状小果的果皮。火棘属的果实不是典型和梨果,是蔷薇科果实在演化过程中的一个过渡类型。火棘属肉质果壁的厚角组织经过角隅减薄后再转变成厚壁组织。     

灵武长枣果实发育结构特征研究

采用石蜡切片法,研究不同发育时期灵武长枣果实的结构特征。结果表明:(1)缓慢生长期细胞增长缓慢,外果皮细胞5~6层,表皮细胞由1层薄壁细胞构成,呈长矩形或长椭圆形,表皮细胞以内的薄壁细胞不断增生,形成内表皮细胞。果实体积增大伴随着空腔的出现,中果皮维管束数量多;(2)第一次快速生长期细胞增长迅速,表皮细胞排列疏松,中果皮中的空腔增大速度最快,维管束主要分布在靠近外果皮和内果皮的中果皮部位;(3)减缓生长期表皮细胞变成圆形或椭圆形等不规则形状,细胞排列松散,内表皮细胞形状、大小不一,细胞排列疏松。中果皮中的空腔继续增大,维管束数目逐渐减少,但变化幅度较小;(4)第二次快速生长期外果皮细胞层数减少到3~4层,表皮细胞和内表皮细胞难以区分,空腔随着果实体积的增大达到最大,许多细胞单列排成网状结构,形成更大的腔,果皮中的维管束分布最少。在灵武长枣果实发育过程中,不同发育时期的不同部位其果实的形态解剖特征不同。     

福尔美对猕猴桃果实发育的影响

应用生长调节剂促进植物生长发育的报道已经很多,但是用于促进果实肥大效果显著的药剂还不多。福尔美(Fulmet)是继赤霉素之后,新开发的植物生长调节剂,是一种能够促进细胞分裂,增加细胞数的人工合成的细胞分裂素,分子式为C_(12)H_(10)。CINO_4O,分子量为247.68,该药剂日本已有市售,它能有效地促进猕猴桃、梨、葡萄等果实增大。近年,大量试验表明,福     

CPPU对猕猴桃果实组织发育及内源细胞分裂素含量的影响

对经生长调节剂ＣＰＰＵ处理的猕猴桃果帝进行了组织学及内源细胞分裂素含量变化的研究。结果表明：处理后的果帝细胞分裂时期延长,细胞的数目增多,体积增大;处理果实中,内源细胞分裂素的含量在果肉细胞分裂盛期及其之后都有所增高。     

中华猕猴桃品种'Hort16A'的果实发育特征

To explore the fruit development characteristics of Actinidia chinensis'Hort16A' , fruit shape indexes during 2-154 d after anthesis, contents of soluble sugar and titratable acid in fruit during 30-154 d after anthesis, and contents of organic acid components in fruit during 44-147 d after anthesis were analyzed. The results show that fruit of 'Hort16A' grows rapidly during 30-44 and 58-72 d after anthesis. Content of soluble solid in fruit during 100-140 d after anthesis is slightly higher than that during 2-93 d after anthesis, and increases rapidly during 147-154 d after anthesis. Fruit firmness decreases rapidly during 147-154 d after anthesis. In general, during 30-154 d after anthesis, content of soluble sugar in fruit increases gradually, while content of titratable acid decreases firstly, then increases, and decreases again. In the fruit, tartaric acid is not detected, content of quininic acid is the highest, contents of malic acid and citric acid are higher, and contents of succinic acid and fumaric acid are very low. Total content of organic acids increases firstly and then decreases, and reaches the highest value at 140 d after anthesis. It is suggested that in order to improve fruit quality of'Hort16A' , its cultivation and management plans will be set up based on fruit development characteristics.     

中国李果实发育的解剖学观察（简报）

中国李(Prunus salicina)原产于我国长江流域,是我国栽培李的基本种。国外对李果实发育研究较多,但多限于欧洲李(P.domestica)。近年来有人研究了“中国李”果实的生长动态,但缺乏进一步的研究。     

狗牙根花序发育过程的形态学观察

对狗牙根(Cynodon dactylon‘C299’)花序发育过程中的形态学变化进行了观察。结果表明,‘C299’花序的整个发育过程可分为8个阶段,即营养生长期、穗轴发生期、苞叶原基分化期、小穗原基分化期、小穗分化期、小花分化期、颖片和内外稃发育期及花药和柱头形成期。其中,穗轴发生期(直立茎上有6~9片叶)是抑制花序形成和决定种子产量的关键时期。     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Synthesis and antimicrobial studies of hydrazone derivatives of 4-[3-(2,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid and 4-[3-(3,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid

Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.