大萼香茶菜丁素的化学结构

从大萼香茶菜叶中又分得一个具有细胞毒活性的新的二萜类化合物,命名为大萼香茶菜丁素(macrocalyxin D)。根据光谱和化学数据鉴定其化学结构为[3]。     

大萼香茶菜辛素的化学结构

大萼香茶菜（Ｒａｂｄｏｓｉａｍａｃｒｏｃａｌｙｘ（Ｄｕｎｎ）Ｈａｒａ）系唇形科（Ｌａｂｉａｔａｅ）香茶菜属植物,民间用于治疗肿瘤等疾病。我们曾报道了它的具有抗菌和细胞毒活性的７个新二萜成分：大萼香茶菜甲素、乙素、丙素、丁素、戊素、己素和庚素［１—５］。进一步研究又分得３个结晶单体。其中,结晶Ⅰ鉴定为新化合物,命名为大萼香茶菜辛素;结晶Ⅱ和Ⅲ鉴定为已知化合物ｏｒｉｄｏｎｉｎ和ｅｎｍｅｎｏｌ。大萼香茶菜辛素（Ⅰ）　Ｃ２２Ｈ３４Ｏ８,ｍｐ２３０℃,［α］２２Ｄ－４１．８（ｃ０．２２,ＭｅＯＨ）。ＩＲ不…     

花锚属一新变型——玉花卵萼花锚

报道了龙胆科卵萼花锚的一个新变型——玉花卵萼花锚。新变型区别于原变型的唯一特征是其花冠为白色,部分花距为黄色。     

贵州省拟大萼苔属Cephaloziella植物的初步研究

在查阅文献和标本的基础上,对贵州省拟大萼苔属Cephaloziella植物进行了系统的整理和研究,初步理清了该属植物在贵州的分布,确认贵州省拟大萼苔属植物有8种1变种。其中,刺茎拟大萼苔C.spinicaulis为贵州新记录种,并提供了该种的详细形态描述。本研究还编制了贵州省拟大萼苔属植物的分种检索表。     

陕西秦岭拟大萼苔科的2个新记录种

报道陕西秦岭的2个苔类新记录种:红色拟大萼苔[Cephaloziella rubella(Nees) Warnst.]和被刺拟大萼苔(Cephaloziella spinicaulis Douin.)。根据标本对2种植物的形态进行了详细的描述,同时对其地理分布进行了简要说明。     

大萼香茶菜乙素和己素的化学结构

从大萼香茶菜［Ｒａｂｄｏｓｉａ ｍ ａｃｒｏｃａｌｙｘ（Ｄｕｎｎ） Ｈａｒａ］叶的乙醇提取物中又分得两种二萜类成分,经ＩＲ、ＭＳ、１ Ｈ－１Ｈ ＣＯＳＹ、１３Ｃ－１ Ｈ ＣＯＳＹ 和ＮＯＥ等光谱分析及衍生物制备,确证其化学结构为新型二萜,分别命名为大萼香茶菜乙素和己素     

贵州紫云产黄花香茶菜的化学成分研究

采用甲醇回流提取和硅胶柱层析方法,从紫云产黄花香茶菜中分离得到6个化合物,结合1H-NMR、13C-NMR数据及文献资料鉴定为黄花香茶菜乙素(Ⅰ)、黄花香茶菜丁素(Ⅱ)、大萼变型香茶菜甲素(Ⅲ)、3β-Hydroxy-18α,19α-urs-20-en-28-oic acid(Ⅳ)、齐墩果酸(Ⅴ)和熊果酸(Ⅵ)。其中化合物Ⅳ为首次从该属植物中分离得到。     

大萼香茶菜庚素的化学结构

从大萼香茶菜（Ｒａｂｄｏｓｉａ ｍ ａｃｒｏｃａｌｙｘ （Ｄｕｎｎ） Ｈａｒａ）叶的乙醇提取物中又分离到３ 个二萜成分（结晶Ⅰ、Ⅱ、Ⅲ）,通过ＩＲ、ＭＳ、１Ｈ－１Ｈ ＣＯＳＹ、１３Ｃ－１Ｈ ＣＯＳＹ和ＮＯＥ等光谱分析及衍生物的制备,确定结晶Ⅰ的结构为ｅｎｔ－７β－２０－ｅｐｏｘｙ－６α, ７α,１４α,１５α,１６α－ｐｅｎｔａｈｙｄｒｏｋａｕｒａｎｅ－１７－ａｃ－ｅｔａｔｅ,为新的二萜化合物,命名为大萼香茶菜庚素;结晶Ⅱ和Ⅲ为已知化合物ｒａｂｄｏｐｈｙｌｌｉｎ Ｈ和ｐｏｎｉｃｉｄｉｎ。     

有关中国细齿缺萼苔(Gymnomitrion crenulatum)和中华缺萼苔(G. sinense)资料

细齿缺萼苔(G. crenulatum Gott. ex Carr.)的中国记录为错误鉴定,标本实为中华缺萼苔(G. sinense K. Muell.),应被移出中国苔藓植物区系。研究发现了多号西藏产中华缺萼苔标本,将中华缺萼苔其在中国的分布范围从云南的模式产地扩展到了西藏。对中华缺萼苔进行了形态特征描述和分布分析,并提供了特征示意图。     

中国囊萼花属一新记录种——茎花囊萼花

首次报道了囊萼花属(Cyrtandromoea Zoll.)的1个中国新记录种——茎花囊萼花(Cyrtandromoea grandis Ridl.),该种原记载产于泰国、马来半岛和苏门答腊岛,2019年在中国云南省勐海县布朗山地区发现有分布。茎花囊萼花与囊萼花(Cyrtandromoea grandiflora C.B.Clarke)最为相似,但前者聚伞花序生于老茎上,每一花序3～18朵花,二者容易区别。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

The structure, reproduction and taxonomy of Vidalia and Osmundaria (Rhodophyta, Rhodomelaceae)

Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.     

New or rare chromosome counts in Artemisia L. (Asteraceae, Anthemideae) and related genera from Kazakhstan

Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.     

肝癌中HBV和HCV基因和抗原的分布及意义

采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细     

Selection with two alleles and complete dominance

For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.