限制性内切酶诱发的姊妹染色单体互换

用限制性内切酶PstⅠ,SalⅠ,PvuⅡ和BamHⅠ处理CHO细胞后,发现其SCE率升高,与对照相比,前三种酶具有显著性差异。但这些酶诱导SCE的效应与其致染色体畸变效应相比则较弱,提示引起DNA双链断裂的限制性内切酶不是SCE的强刺激物。实验结果表明,BrdU取代胸苷不能消除限制酶对底物DNA的识别及裂解。     

中国的红树林

我国红树林主要分布在热带及亚热带沿海盐滩和河川出口的冲积盐性土上,包括24个科,47种,属于东方群系。从广西钦州湾开始经北海港,沿雷州半岛的海安分为两支,一支往南经海南岛的儋县新英港,向东经琼山县的东寨港和文昌县的清澜港,沿着东海岸至崖县的三亚港,又折向北到达东方县的八所港;另一支向东北经湛江的赤坎,阳江的海陵岛,台山的上下川岛,中山的三灶岛,新会的崖门,再沿海岸往北至福建的福鼎和台湾的新竹港。根据我国红树林的主要构成种类、外貌、生境,大致可分为3大群系和10个群落。(1) 矮灌木群系——这个群系多见于纬度稍高的海滩前缘,包括海榄雌群落和桐花树群落。这些群落在演替上处于前期阶段。(2) 高大稠密灌木群系——这个群系由于气温、年降雨量的差异和土壤性质的不同,组成这个群系的种类也有不同,不过都是以红树族的种类为建群种,它包括4个群落:红树群落、红海兰群落和角果木群落,这些群落在演替上属于中期阶段。(3) 乔木群系——这个群系主要分布在海南岛东北和东部海岸,所在地一般地势较高,前缘地带每日潮涨仍有海水浸淹。后缘地带只有每月大潮时才有海水到达,土壤比较固结,它包括木榄群落、海莲和尖瓣海莲群落、海桑群落及半红树林水椰群落。这些群落在演替上是处于后期阶段。组成我国红树林的种类大多数都具有较高的经济价值,如角果木是优质单宁的原料,有些种类经过发酵处理成为高营养的饲料和肥料。此外,沿海浮游生物的产量有红树林比无红树林的地带高达7倍,因此加强对红树林的经营和保护应采取积极态度和有效措施。     

中国的红树林

我国红树林主要分布在热带及亚热带沿海盐滩和河川出口的冲积盐性土上,包括24个科,47种,属于东方群系。从广西钦州湾开始经北海港,沿雷州半岛的海安分为两支,一支往南经海南岛的儋县新英港,向东经琼山县的东寨港和文昌县的清澜港,沿着东海岸至崖县的三亚港,又折向北到达东方县的八所港;另一支向东北经湛江的赤坎,阳江的海陵岛,台山的上下川岛,中山的三灶岛,新会的崖门,再沿海岸往北至福建的福鼎和台湾的新竹港。根据我国红树林的主要构成种类、外貌、生境,大致可分为3大群系和10个群落。(1) 矮灌木群系——这个群系多见于纬度稍高的海滩前缘,包括海榄雌群落和桐花树群落。这些群落在演替上处于前期阶段。(2) 高大稠密灌木群系——这个群系由于气温、年降雨量的差异和土壤性质的不同,组成这个群系的种类也有不同,不过都是以红树族的种类为建群种,它包括4个群落:红树群落、红海兰群落和角果木群落,这些群落在演替上属于中期阶段。(3) 乔木群系——这个群系主要分布在海南岛东北和东部海岸,所在地一般地势较高,前缘地带每日潮涨仍有海水浸淹。后缘地带只有每月大潮时才有海水到达,土壤比较固结,它包括木榄群落、海莲和尖瓣海莲群落、海桑群落及半红树林水椰群落。这些群落在演替上是处于后期阶段。组成我国红树林的种类大多数都具有较高的经济价值,如角果木是优质单宁的原料,有些种类经过发酵处理成为高营养的饲料和肥料。此外,沿海浮游生物的产量有红树林比无红树林的地带高达7倍,因此加强对红树林的经营和保护应采取积极态度和有效措施。     

St14/TaqⅠRFLPs在甲型血友病基因探测与产前基因诊断中的应用

<正> 甲型血友病是最常见的遗传性凝血疾病,是由于凝血因子Ⅷ(FVⅢ)基因缺陷所致。目前对此病尚无满意的治疗方法。利用DNA分析技术进行甲型血友病基因检测与产前基因诊断对开展优生优育有重要的实际应用价值。由于FⅧ基因组织结构庞大,分子病理改变复杂,目前多采用DNA限制酶片段长度多态性(RFLPs)为遗传标志对有缺陷的FⅧ基因进行连锁分析。St 14(DXS52)是人X染色体长臂远端的一段基因外DNA序列,与FⅧ基因紧密连锁。国外已将St14/Taq Ⅰ RFLPs用于甲型血友病基因携带者的检测,但尚未见到用于产前基因诊断的报道。我们利用引进的St14片段为探针,采用简化的低脂奶粉杂交体系和DNA凝胶原     

猪肺炎支原体膜上ATP酶生化性质的研究

猪肺炎支原体膜上ATP酶为Mg~(2+)激活,乌巴因不抑制。DCCD和寡霉素对该酶也无抑制作用,只有NBD与Quercetin才有一定的抑制效果。用梯度凝胶电泳可获均一的具有活性的酶蛋白带。     

The effects of temperature and pH on the ethanol tolerance of the wine yeasts, Saccharomyces cerevisiae, Candida stellata and Kloeckera apiculata

The influences of temperature and pH on the survival and growth of Saccharomyces cerevisiae, Candida stellata and Kloeckera apiculata were examined in the presence of ethanol concentrations between 2.5 and 15% v/v. At 15°C, the maximum concentrations of ethanol permitting the growth of S. cerevisiae, C. stellata and K. apiculata were 15%, 11% and 9%, respectively. These maximum concentrations were decreased at 10°C and 30°C. Cells of S. cerevisiae showed no loss in viability when incubated for 12 d at 10°C or 15°C in the presence of 15% ethanol but showed some loss at 30°C. Cells of C. stellata were tolerant of 12.5% ethanol at 10°C and 15°C but not at 30°C. Cells of K. apiculata were tolerant of 10–12.5% ethanol at 15°C but not at 10°C or 30°C. Sensitivity of the yeast cells to ethanol was marginally increased on decreasing the pH from 6-0 to 3–0.     

Comparative analysis of glycoprotein and glycolipid composition of virulent and avirulent strain membranes ofMycoplasma hyopneumoniae

The glycoproteins and glycolipids from membranes of virulent strain Z and avirulent strain M ofMycoplasma hyopneumoniae have been compared. The proteins and the glycoproteins were identified by SDS-polyacrylamide gel electrophoresis and concanavalin A-biotin labeling, respectively. The membrane preparation contained approximately 34 protein bands with molecular weights between 20 KD and 100 KD. The concanavalin A-biotin system reacted with a glycoprotein of a molecular weight of approximately 28,000 from avirulent strain M and did not react with the correspondent band from virulent strain Z. The membrane glycolipids of both strains consisted of monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG), and the percentages of 160, 180, and 181 fatty acids comprised more than 80% of the total fatty acids of membrane glycolipids. The 180 fatty acid of MGDG in avirulent strain M was twofold higher than that of virulent strain Z.     

Expression of an enhancer-binding protein in insect cells transfected with the Autographa californica nuclear polyhedrosis virus IE1 gene.

The baculovirus Autographa californica nuclear polyhedrosis virus contains an element known as homologous region 5 (hr5) which is an enhancer of delayed-early viral gene expression. To begin to identify proteins that interact with hr5, DNA-protein interactions were analyzed by using extracts from Spodoptera frugiperda cells and a fragment of DNA containing the left half of the hr5 enhancer. This 252-bp DNA fragment contains two copies of a 30-bp direct repeat (DR30) and two copies of a 24-bp imperfect palindrome contained within a 60-bp direct repeat (DR60). Extracts prepared from normal S. frugiperda cells and cells transfected with pUC8 lacked enhancer-binding proteins. However, when gel shift assays were performed with extracts from cells transfected with a plasmid containing the viral trans-activator IE1 gene, two DNA-protein complexes were formed. Both DNA-protein complexes were specifically inhibited by competition with a 60-bp oligonucleotide corresponding to DR60 but not by competition with a different oligonucleotide corresponding to DR30. Formation of the two complexes did not appear to involve cooperative interactions between binding proteins. When DR60 was used as a probe, a single complex was formed. To measure the enhancer activity of DR60, a reporter plasmid was constructed that contained DR60 cloned upstream of the reporter chloramphenicol acetyltransferase gene under the control of the delayed-early 39K promoter. Transient expression analysis indicated that the oligonucleotide increased expression of this gene 300-fold over the level obtained in the absence of any enhancer sequences.     

Monoclonal Antibodies against Apple 1-Aminocyclopropane-l-Carboxylate Synthase

1-Aminocyclopropane-l-carboxylate (ACC) synthase from applefruits was purified over 5,000-fold by conventional column chromatography.By immunizing mice with this partially purified enzyme preparation,8 hybridoma lines producing monoclonal antibodies against appleACC synthase were isolated. While all 8 clones immunoprecipitatednative ACC synthase, only two clones recognized the putative(48 kDa) ACC synthase on Western blots. When a partially purifiedACC synthase preparation was incubated with S-adenosyl-L-[carboxyl-¹⁴C]methionine(AdoMet), only one radioactive protein of 48 kDa was detectedon sodium dodecyl sulfate-poly-acrylamide gel electrophoresis.This radioactive protein was specifically immunoprecipitatedby the monoclonal antibodies, indicating that apple ACC synthaseis specifically radiolabeled by its substrate AdoMet, as istomato ACC synthase. Thus, the monoclonal antibodies recognizedboth native and AdoMet-inactivated forms of ACC synthase. Whilethese antibodies failed to im-munoprecipitate ACC synthase isolatedfrom ripe tomato fruits, ripe avocado fruits or auxin-treatedmungbean hypocotyls, they were effective in immunoprecipitatingthe enzyme isolated from ripe pear fruits. (Received August 11, 1990; Accepted October 17, 1990)