虫草多型现象的5.8SrDNA和ITS2序列测定研究

新定名的甘肃虫草Cordyceps gansuensi与冬虫夏草Cordyceps sinensi形态相似。 蛹虫草Cordyceps militaris具有拟青霉型（Paecilomyces-type）和轮枝孢型（Verticillium-type）两类无性型。此研究对5.8S rRNA基因 及ITS2间区DNA序列的分析结果表明,甘肃虫草和冬虫夏草的DNA序列相同,属于同一种;蛹虫草的两类无性型具有分子水平上的遗传趋异性。     

虫草多型现象的5.8S rDNA 和ITS2 序列测定研究

新定名的甘肃虫草Cordycepsgansuensi与冬虫夏草Cordycepssinensi形态相似。蛹虫草Cordycepsmilitaris具有拟青霉型（Paecilomyces-type）和轮枝孢型（Verticillium-type）两类无性型。此研究对5.8SrRNA基因及ITS2间区DNA序列的分析结果表明,甘肃虫草和冬虫夏草的DNA序列相同,属于同一种;蛹虫草的两类无性型具有分子水平上的遗传趋异性。     

2株北虫草菌株系统发育及其活性成分含量分析

对收集的2株北虫草菌株进行形态学观察、分子鉴定及子实体中主要活性成分含量分析,为其应用研究提供技术支持。采用平板培养法、玻片培养法及显微观察对2株北虫草菌株进行形态学观察;基于ITS序列分析对2株实验菌株进行分子鉴定;有效成分的测定均采用高效液相色谱法。结果表明,2株北虫草子实体形态及在PDA加富培养基上菌丝长势、菌落形态差异显著,ITS序列分析结果显示,2株北虫草为蛹虫草,属种内差异;二者腺苷成分相近,但尖头北虫草虫草素的含量是大孢子头北虫草的2倍,且同一品种不同栽培方法及同一种源不同栽培地获得的子实体中两种活性成分的含量有所不同,尤其是腺苷的含量差异明显。以北虫草子实体的品相作为品质优劣的评估标准缺乏科学依据,在子实体应用过程中应根据需要科学选择。     

台湾虫草子实体人工培养条件的初步研究

目的研究人工培养条件对台湾虫草子实体形成的影响。方法通过黄山被毛孢的液体摇瓶培养,确定摇瓶种子的最佳培养时间,并研究了在人工诱导下台湾虫草子实体的形成条件,即子实体形成与营养液pH、营养液量、培养温度及光照时间之间的关系。结果黄山被毛孢液体摇瓶最佳培养时间为12 d,人工固体培养子实体所需营养液最佳pH为6.0,营养液量为40 mL,培养温度为25℃,菌丝培养阶段为完全黑暗培养,原基出现后给予光照,可获得较多的子实体。结论人工培养条件对台湾虫草菌丝体生长、原基形成、子实体产量具有显著影响。     

基于5.8S rDNA-ITS序列的我国浙江沿海铜藻群体遗传多样性分析

为了调查我国浙江沿海铜藻(Sargassum horneri)群体遗传多样性,对浙江省南麂岛火焜岙、洞头岛、枸杞岛的野生群体和南麂岛马祖岙养殖群体的铜藻44个样品的5.8S rDNA-ITS序列进行了PCR扩增和序列分析,获得DNA片段长度为1485 bp,包括部分ITS1、完整的5.8S rDNA和部分ITS2序列。序列分析表明仅有1个变异位点,说明群体间没有明显的遗传分化,遗传多样性较低。另外,将包含这一变异位点的基因型与GenBank公共数据库中另外2株铜藻的5.8S rDNA-ITS区序列进行比对,共有31个变异位点,其中插入/缺失位点10个。因此,建议加快人工铜藻场的建设以及野生铜藻场的恢复,保持铜藻场的生态平衡。     

枇杷属内栽培种和部分野生种ITS序列分析

对不同栽培区的25种普通枇杷品种以及7种枇杷属野生种的ITS序列进行扩增并测序,采用邻接法和最大简约法进行系统发育树的构建并对枇杷属内不同种间的遗传关系进行了分析。结果表明:枇杷属植物ITS序列ITS1+5.8S rDNA+ITS2总长度为592 bp或594 bp,长度变化发生在ITS2。所有样本的ITS1和5.8S rDNA长度一样,都是223 bp和168 bp;而ITS2为201 bp或203 bp。5种枇杷属野生种的ITS序列长度为594 bp,包括栎叶枇杷、大渡河枇杷、南亚枇杷、南亚枇杷窄叶变种和大瑶山枇杷;其余2种枇杷属野生种(麻栗坡枇杷、小叶枇杷)和普通枇杷栽培种的ITS序列长度都为592 bp。所有样本ITS序列的GC含量为64.2%~64.5%,其中ITS1为64.1%~65.5%,ITS2为68.1%~72.6%。对所有样本的ITS序列比对产生44个可变位点,其中38个为简约信息位点,其中11个位于ITS1,5个位于5.8S rDNA,22个位于ITS2。最大的种间序列差异为7.7%,最小的种间差异发生在麻栗坡枇杷和小叶枇杷之间,仅为0.2%。普通枇杷种内的ITS序列差异很低,25种普通枇杷栽培种之间的序列差异为0~1.5%。所研究的枇杷属植物可分为3个分支。分支Ⅰ包括所有普通枇杷品种,分支Ⅱ包含5种野生枇杷种,包括栎叶枇杷、大渡河枇杷、南亚枇杷、南亚枇杷窄叶变种和大瑶山枇杷;分支Ⅲ由2个野生枇杷种(麻栗坡枇杷、小叶枇杷)组成。该研究结果表明ITS序列对枇杷种间鉴定和系统发育分析具有一定意义,但对普通枇杷栽培种间的鉴定作用不大。     

下垂虫草的重寄生现象及重寄生菌的鉴定

在安徽省岳西县鹞落坪自然保护区,发现了1种寄生于下垂虫草(Ophiocordyceps nutans)的重寄生菌。通过形态特征观察和ITS序列分子生物学分析,将其鉴定为枝多头霉(Polycephalomyces ramosus)。其孢梗束着生于下垂虫草子实体的可孕部,顶部膨大呈球形。本种具有产生单个卵形的A型分生孢子的顶侧生排列的A型瓶梗和能形成分生孢子链的B型瓶梗,并在培养基上的气生菌丝和孢梗束的柄部都观察到梭形、链生的B型分生孢子。GenBank中相关种的ITS序列与拉丁名可能有误。     

福建橄榄18S-26S rRNA及其ITS片段的克隆与序列分析

利用18S-26S rRNA基因及其ITS片段的PCR扩增、克隆及测序分析,对福建14个橄榄品种进行分子标记及遗传分类。序列分析结果表明:14个品种可分为4个类别,以1号品种为参照,3、4、6、7、8、9、11号品种的ITS1、ITS2和5.8S共634个碱基序列完全一致,与1号仅ITS2上有1个碱基差异,2号和1号品种的ITS1和5.8S序列完全一致,仅ITS2上有2个碱基差异,归为第一类;5号和14号的序列完全一致,与1号在ITS1和ITS2上各有1个碱基差异,归为第二类;10号和12号序列完全一致,与1号在ITS1上有2个碱基差异,归为第三类;13号品种5.8S的序列与1号相同,但在ITS1上有1个碱基差异,在ITS2上有24个碱基差异,归为第四类。使用DNAMAN软件建立的同源关系树说明了不同橄榄品种的变异程度。将橄榄18S-26S rRNA基因及其ITS序列登陆GenBank,登陆号:DQ517524。     

亚稀褶黑菇和稀褶黑菇的ITS序列分析

对亚稀褶黑菇和稀褶黑菇的ITS全序列进行了测定和比较,首次报道了亚稀褶黑菇的ITS1和5.8S区域.在ITS区域中,不同采集地的亚稀褶黑菇与稀褶黑菇的5.8S rDNA具有100%的同源性,而两侧ITS之间表现出种内和种间的多态性,种内的差异均不超过5%,种间的差异达10%左右.ITS序列分析方法可以作为两者的鉴定方法.     

亚稀褶黑菇和稀褶黑菇的ITS序列分析

对亚稀褶黑菇和稀褶黑菇的ITS全序列进行了测定和比较,首次报道了亚稀褶黑菇的ITS1和5.8S区域。在ITS区域中,不同采集地的亚稀褶黑菇与稀褶黑菇的5.8S rDNA具有100%的同源性,而两侧ITS之间表现出种内和种间的多态性,种内的差异均不超过5%,种间的差异达10%左右。ITS序列分析方法可以作为两者的鉴定方法。     

壳聚糖酶的克隆表达与壳寡糖的制备分析

目的:克隆壳聚糖酶基因于大肠杆菌中实现高表达,制备壳寡糖。方法:以枯草芽孢杆菌总DNA为模板扩增壳聚糖酶基因(CSN),克隆至载体pET23a(+)上,转化菌株BL21(DE3)。重组子经0.5 mmol/L IPTG诱导后,SDS-PAGE和质谱检测与鉴定重组酶。酶纯化后水解壳聚糖,薄层色谱分析其水解产物。结果:质谱证明壳聚糖酶(31.5kDa)成功表达,表达量占菌体总蛋白的45%左右。纯化后重组酶浓度为900 mg/L,纯度95%、回收率85%,酶活力为10 000 U/mg。壳聚糖降解产物为壳二糖至壳四糖。结论:原核表达载体pET23a(+)-CSN构建正确,壳聚糖酶表达量与活性高,适用于水解壳聚糖制备壳寡糖。     

国内外蝗害治理技术现状与展望

本文首先概述了国内外蝗虫发生与为害的态势,总结了现阶段我国蝗虫发生与为害的主要特点:即农田飞蝗暴发频繁而且严重,草原土蝗的发生时常造成严重的经济损失,而且侵入城市干扰市民生活,我国与周边国家之间蝗虫过境迁移频繁,使用化学农药污染环境和农产品;分析了国内外蝗虫防治对策与技术的发展现状,重点介绍了应急防治和可持续治理对策、...     

Molecular characterisation of species and genotypes of Cryptosporidium and Giardia and assessment of zoonotic transmission

The molecular characterisation of species and genotypes of Cryptosporidium and Giardia is essential for accurately identifying organisms and assessing zoonotic transmission. Results of recent molecular epidemiological studies strongly suggest that zoonotic transmission plays an important role in cryptosporidiosis epidemiology. In such cases the most prevalent zoonotic species is Cryptosporidium parvum. Genotyping and subtyping data suggest that zoonotic transmission is not as prevalent in the epidemiology of giardiasis. Molecular characterisation of Cryptosporidium and Giardia is a relatively recent application that is evolving as new genes are found that increase the accuracy of identification while discovering a greater diversity of species and yet unnamed taxa within these two important genera. As molecular data accumulate, our understanding of the role of zoonotic transmission in epidemiology and clinical manifestations is becoming clearer.     

Synthesis and turnover of cerebrosides and phosphatidylserine of myelin and microsomal fractions of adult and developing rat brain.

The synthesis and turnover of cerebrosides and phospholipids was followed in microsomal and myelin fractions of developing and adult rat brains after an intracerebral injection of [U-14C]serine. The kinetics of incorporation of radioactivity into microsomal and myelin cerebrosides indicate the possibility of a precursor-product relationship between cerebrosides of these membranes. The specific radioactivity of myelin cerebrosides was corrected for the deposition of newly formed cerebrosides in myelin. Multiphasic curves were obtained for the decline in specific radioactivity of myelin and microsomal cerebrosides, suggesting different cerebroside pools in these membranes. The half-life of the fast turning-over pool of cerebrosides of myelin was 7 and 22 days for the developing and adult rat brain respectively. The half-life of the slowly turning-over pool of myelin cerebrosides was about 145 days for both groups of animals. The half-life of the rapidly turning-over microsomal cerebrosides was calculated to be 20 and 40 h for the developing and adult animals respectively. The half-life of the intermediate and slowly turning-over microsomal cerebrosides was 11 and 60 days respectively, for both groups of animals. The amount of incorporation of radioactivity into microsomal cerebrosides from L-serine was greatly decreased in the adult animals, and greater amounts of the precursor were directed towards the synthesis of phosphatidylserine. In the developing animals, considerable amounts of cerebrosides were synthesized from L-serine, besides phosphatidylserine. The time-course of incorporation indicated that a precursor-product relationship exists between microsomal and myelin phosphatidylserine. The half-life of microsomal phosphatidylserine was calculated to be about 8 h for the fast turning-over pool in both groups of animals.     

白术同源四倍体的诱导和鉴定及其与二倍体过氧化物酶的比较

以白术（Atractylodes macrooephala Koidz.）二倍体组培苗为材料,对其四倍体诱导方法进行研究,共获得45个白术同源四倍体株系,为优良株系的选育提供了材料。此外,还分析比较了其中8个白术四倍体株系与二倍体的过氧化物酶同工酶（POD）的酶谱差异,发现四倍体各株系过氧化物酶同工酶谱比二倍体的均多了Rf0.310的谱带,且总过氧化物酶比活力也发生了很大改变,对探讨白术四倍体优良株系的生理生化机理具有一定的参考价值。     

Identification and composition of the tonsillar and anal enterococcal and streptococcal flora of dogs and cats

Enterococcus faecalis was the most frequently isolated enterococcal species from anal swabs and tonsils of dogs and cats, although in the anal samples from dogs Ent. hirae was found almost as often as Ent. faecalis. Most Ent.faecium strains from dog tonsils differed from those associated with humans and other animals in that they fermented sorbitol. Typical Ent. avium as well as atypical Ent. avium -like strains were seen in dogs, while the related species Ent. raffinosus was associated with cat tonsils. Enterococcus cecorum also occurred mainly in cats. Certain atypical strains, presumptively identified as Ent. cecorum , shared characteristics with Ent. columbae.
The most frequent streptococcal species in tonsils of cats and dogs were Streptococcus suis and Strep. canis. Streptococcus canis and Strep. bovis predominated in anal swabs. The canine Strep. suis differed from the common porcine strains in fermenting mannitol.
Forty-seven of the 288 isolates examined could not be identified or related to known species. The characteristics of two groups of these bacteria, provisionally called 'Ton 31 group' and 'O7 group' are described.