高频彩色多普勒超声对乳腺癌腋窝淋巴结性质的鉴别价值

目的:研究高频彩色多普勒超声对乳腺癌腋窝良性淋巴结与腋窝转移性淋巴结的鉴别价值。方法:选择2015年2月~2016年6月在我院进行诊治的乳腺癌患者150例,应用高频二维超声结合彩色多普勒血流显像技术,观察腋窝肿大淋巴结的声像图及血流情况。结果:经二维超声发现,乳腺癌腋窝良性淋巴结的皮质多向心增厚(68.93%)、长短径比L/S多2.0(70.58%)、多不融合(93.14%)、多无钙化斑(97.06%);腋窝转移性淋巴结的皮质多偏心增厚(68.48%)、长短径比L/S多2.0(69.57%)、多融合(68.48%)、多有钙化斑(77.17%);两者相比有明显差异(P0.05);经彩色多普勒血流显像技术发现,乳腺癌腋窝良性淋巴结的血流信号分布多呈门型(63.17%),血流丰富程度多为Ⅱ级(54.35%);腋窝转移性淋巴结的血流信号分布多呈周边型(68.93%),血流丰富程度多为Ⅲ级(72.83%);两者相比有明显差异(P0.05)。结论:乳腺癌腋窝良性淋巴结与腋窝转移性淋巴结在内部回声、形态、血流分布特点等方面有显著的差异,高频彩色多普勒超声对乳腺癌腋窝良性淋巴结与腋窝转移性淋巴结具有较高的鉴别价值。     

栀子带芽茎段愈伤组织诱导分化及丛生芽增殖和生根研究

以栀子带芽茎段为试材,对其愈伤组织诱导分化及丛生芽增殖与生根进行初步研究。结果表明,栀子带芽茎段愈伤组织快速诱导和分化最佳培养基是MS+KT 1 mg/L+NAA 0.05 mg/L;栀子带芽茎段丛生芽增殖和生根最佳培养基是MS+KT 2.0 mg/L+NAA 0.05 mg/L。     

欧美黑杨离体再生途径及影响因子的研究

先期完成了以腋芽发育为再生方式的研究后 [1 ] ,又对不定芽的发育进行了探索 .分别以欧美黑杨特选品系的不同部位外植体进行愈伤组织诱导及植株再生研究 ,易诱导并易分化出新芽的外植体为幼嫩茎段 ;通过不同激素浓度合理配比 ,进行适宜的诱导及分化培养基筛选 ,培养基为 MS+6 - BA 1.2 mg/ L +NAA 0 .5 mg/ l,附加 6g/ L琼脂 ,诱导的愈伤组织分化出密集的再生芽 ;糖分在诱导分化过程中作用突出 ,其合适浓度为 4 0 g/ L ;愈伤组织的形态及培养时间对分化频率影响较大 ,最佳的形态为致密的绿色 ,白色及粉红色的愈伤组织较疏松 ,分化率很低 .不同部位外植体、激素含量、蔗糖浓度、愈伤组织形态及培养时间是明显影响欧美黑杨愈伤组织诱导分化的因子 .     

Isolation and characterization of anthocyanin 5-O-glucosyltransferase from flowers of Dahlia variabilis

In the cyanic flowers ofDahlia variabilis (Asteraceae), an enzyme was demonstrated which catalyzes a glucosyl group transfer from UDP-glucose to the 5 position of anthocyanidin 3-O-glucoside and 3-O-malonylglucoside. The anthocyanin 5-O-glucosyltransferase (5GT) was purified 88-fold at 8 percnt; yield by (NH₄)₂SO₄ precipitation followed by successive chromatography on DEAE-cellulose, Sephacryl S-200 and Mono P. 5GT exhibited a pH optimum at 8.0 and a pI of 4. 2. Its apparent molecular weight calculated from Sephacryl S-200 was 53 kDa. Its activity was stimulated by 2-ME and DTE but strongly inhibited by PCMB and NEM. It was slightly activated by Mg²⁺ and Ca²⁺ but strongly inhibited by Hg²⁺, Zn²⁺, Cu²⁺, Mn²⁺, Fe³⁺ and Al³⁺. No effect of EDTA was observed. The apparent Km values for cyanidin 3-O-glucoside, cyanidin 3-O-(6′′-O-malonyl)glucoside and UDP-glucose were 120 μmol/L, 75 μmol/L and 250 μmol/L, respectively. Pelargonidin 3-O-glucoside and malonylglucoside were also considerable substrates, but low relative activity was observed for delphinidin 3-O-glucoside which has yet not been found inDahlia flowers.Dahlia 5GT showed substrate specificities different from those reported forSilene, Petunia, Matthiola andPerilla. Neither ADP-glucose nor UDP-galactose could serve as glycosyl donor.     

In vitro plant regeneration in Holarrhena antidysenterica wall., through high-frequency axillary shoot prolieferation

Summary An efficient, rapid and large-scale propagation of the woody, aromatic and medicinal shrub, Holarrhena antidysenterica, through in vitro culture of nodal segments with axillary buds, is described. N⁶-benzyladenine used at 15 μM was the most effective in inducing bud break and growth, and also in initiating multiple shoot proliferation at the rate of 43 microshoots per nodal explant with axillary buds, after 30 d of eulture. By repeated subculturing of nodal explants with axillary buds, a high-frequency multiplication rate was established. Efficient rooting was achieved with 35 μM indole-3-butyric acid which was the most effective in inducing roots, as 80% of the microshoots produced roots. Plantlets went through a bardening phase in a controlled plant growth chamber, prior to ex vitro transfer Micropropagated plants established in garden soil were uniform and identical to donor plants with respect to growth characteristics and vegetative morphology.     

A Preliminary Study on Direct Regeneration of Flower Buds from Peduncle Calli in Dracaena fragrans cv. massangeana

Flower buds were directly regenerated from calli in vitro in the woody plant Dracaena fragrans cv. massangeana Hort. On modified MS medium supplemented with 1.0 mg/L 6-BA and 1.0 mg/L IBA, two kinds of calli, A and B, were formed from the peduncle explants cultured for 5 months. Calli A were loose and on their surface there were many irregular granule-like structures (GLC); Calli B were compact and had bigger tumor-like structures (TLC) on their surface. When the GLC and TLC were transferred onto the medium respectively with 0.4 mg/L 6-BA and 1.0 mg/L IBA, flower buds were differentiated directly from the GLC but only vegetative buds and roots were differentiated from the TLC after culturing for 4 weeks. The GLC could be partly transformed into TLC in the continuous passage culture. Assays on hormones revealed that at a fixed IBA concentration of 0.4 mg/L the defferentiation frequency of flower budding was increased as the 6-BA concentration was decreased from 2.0 mg/L to 10 mg/L. Alternatively, at a fixed 6-BA concentration of 2.0 mg/L, the flower budding frequency was increased when the IBA concentration was changed from 0.4 mg/L to 1.0 mg/L. Moreover, the addition of 2.0 mg/L zeatin to the culture medium containing 2.0 mg/L 6-BA and 0.4 mg/L IBA was favorable to the regeneration of the flower buds. Nevertheless supplementing 1.0 mg/L GA3 into the medium on which the calli had differentiated into flower buds, the flower buds would gradually wither after 2 weeks in culture.     

党参的离体培养及植株再生的研究

在附加激素的MS培养基上,培养党参下胚轴和无菌芽切段,诱导产生愈伤组织并且再生植株。经过两年多(15个世代)的继代培养,建立了党参体细胞无性系。实验结果表明:(1)培养基MS 0.4mg/L 2,4-D 0.8mg/L Kt 2.0mg/L IAA对愈伤组织诱导及继代培养,MS 0.2mg/L 6-BA诱导外植体产生丛芽和愈伤组织再分化,MS 0.5mg/L NAA 0.2mg/L 6-BA及MS 0.2mg/L NAA诱导生根效果最好。(2)愈伤组织再分化经过胚状体途径。     

Establishment of Salt Stress Tolerant Rice Plants Through Step Up NaCl Treatment In Vitro

Establishment of salt tolerant rice plants was examined by single step or step up NaCl treatments of shoot bud clumps in vitro, and variation among in vitro salt tolerant plants were examined by rapid amplified polymorphic DNA (RAPD). Shoot bud clumps were necrotic, stubbed or dead when subjected to single step treatment with 1.5 or 2.0 % NaCl. Conversely all the clumps could grow vigorously when subjected to step up salt treatment with 0.5, 1.0, 1.5 and 2.0 % NaCl at 3 week intervals and 2 % NaCl tolerant plants were established. RAPD revealed shoot bud clumps with and without different NaCl treatments, seedlings from field and grown in vitro, and regenerants from callus were genetically close to one another. Conversely, callus cultures were genetically isolated. Growth under different salt stress conditions was not correlated with the genetic variation, suggesting that 2.0 % NaCl tolerant plants might not result from genetic mutation but were due to adaptation of plants by step up NaCl treatment in vitro.     

铁炮百合组培中不定芽形成的细胞学观察

以铁炮百合鳞片诱导的无菌苗叶段作外植体,在MS+6-BA2.0mg/L+NAA0.2mg/L培养基上诱导不定芽,效果较好。诱导过程中定期取样进行石蜡制片,观察不定芽分化过程中的细胞组织学变化。结果表明,脱分化始于切口周围的细胞;形态发生的主要方式是由愈伤组织分化出不定芽,不定芽通常起源于愈伤组织团从外到内第2~7层细胞的分生细胞团。     

舞钢玉兰芽种类与成枝成花规律的研究

报道了舞钢玉兰芽的种类、分枝习性与成枝生长规律,拟花蕾、着生位置、解剖结构及其分化发育成花规律。从中发现：（1）当年生枝上有休眠芽、叶芽（侧叶芽和顶叶芽）、拟花蕾3种;（2）拟花蕾有缩台枝、芽鳞状托叶、雏枝、雏芽及雏蕾组成,因其外形似“花蕾“,称为“拟花蕾“;（3）缩台枝是枝与花着生的中间过滤枝变阶段,是由母枝顶端节间缩短、增粗的枝段和当年由雏枝生长的1次极短新枝所组成;（4）4-5月及7-8月前后两批形成的拟花蕾,均经过未分化发育期、花被分化发育期、雄蕊群分化发育期及离心皮雌蕊群分化发育期,各期均依次递后交错进行,但不逆转,也不能截然分开,直到翌春花分化发育全部结束,开花后才能结实;（5）芽鳞状托叶是托叶的变态,最外层薄革质,外面密被短柔毛,始落期6月中下旬,其余纸质--膜质,外面密被或疏被毛柔毛,翌春开花时脱落完毕;（6）雏蕾有雏梗、雏花及包被雏花的佛焰苞状托叶组成;（7）分枝习性与成枝生长规律与预生分枝及预生一同生分枝呈单阶无歧、单阶1歧生长规律,稀有单阶2歧生长规律。