血浆蛋白粉对早期断奶仔猪的作用与应用研究概述

本文对血浆蛋白粉的特点、血浆蛋白粉对早期断奶仔猪的影响和在饲料中如何合理利用作一综述，为血浆蛋白粉的合理应用提供一定的理论基础．     

瞬时表达比较马铃薯X病毒CP基因3种结构对RNA沉默的诱导效果

RNA沉默是植物抵御病毒侵染的一种防卫机制,病原来源的抗性(pathogen-derived resistance,PDR)被认为是通过RNA沉默起作用的.转化的核酸片段在基因组中的位置、长短和不同排列结构等均影响RNA沉默的效率.用全长马铃薯X病毒(PVX)CP基因构建非翻译的正义、反义和反向重复结构转基因的植物表达载体,通过农杆菌渗入法瞬时表达测试了这些转基因对RNA介导抗性的诱导效率和有效性.结果表明,反向重复的PVXCP是更为有效的RNA沉默诱导因子,同时也证明让目的基因在受试植物中瞬时表达,在转化植物之前能比较快速地检测转基因的表达情况以及表达产物的功能,从而节约时间和资源,并减少盲目性.图3表2参21     

表达马铃薯Y病毒外壳蛋白基因的转基因烟草抗病机制

根据已报道的马铃薯Y病毒坏死株系(PVY^N)核苷酸序列，克隆了PVY^N外壳蛋白(CP)基因，通过根癌农杆菌(Agrobacterium tumefaciens)LBA4404介导的方法，转化烟草NC89，获得了38株PCR呈阳性的转基因植株．攻毒试验发现，转基因植株对PVY^N的抗性水平存在着差异，其中有4株表现为高度抗病性．Southern blot表明，PVY^N CP基因已经整合到烟草染色体中，转基因的拷贝数与植株的抗病性成正相关．Northern blot表明，PVY^N CP基因在RNA水平上得到了表达，而且PVY^N CP RNA在细胞中的积累量与转基因植株的抗病性呈明显的负相关．Western blot表明，高度抗病植株未检测到转基因CP蛋白质，而抗病和感病植株都检测到了PVY^N CP蛋白，且不同抗性的转基因植物中转基因蛋白质的积累有一定的差异．实验结果表明，表达PVY^N CP基因的转基因烟草其抗病机制类似于转录后的基因沉默，即抗病件可能是RNA介导的．     

圈养亚成体大熊猫日粮粗蛋白表观消化率的初步研究

研究了7只1.5-4.7岁的亚成体大熊猫对23种日粮粗蛋白的表观消化率（ADCP），结果为37．86％－83．70％。分析表明，对1．5－2．5岁的大熊猫，粗纤维采食量与ADCP有极显著的负相关关系（图1）；对2．5－4．7岁的大熊猫。粗纤维采食量与ADCP没有明显相关关系（表3）。对1．5－2．5岁大熊猫，随竹粗蛋白占总粗蛋白比值升高，ADCP呈下降趋势（图2）；2．5－4．7岁的大熊猫，ADCP随竹粗蛋白比例升高而呈上升趋势（图3）；不同大熊猫ADCP还有个体差异。图3表3参10     

Ecological modelling Internet resources

Internet resources are grouped into registers and sources of ecological models (6 addresses), sources of documents (7), sources of data (5), initiatives (5), societies (4), journals (4) frequently asked questions (7), extensive list of links to Web pages (4), search engines (5) and Usenet groups (10). At present, Internet resources are not replacing classical libraries but should be considered as complementary sources of information.     

大豆蛋白和屠宰废水处理工艺研究

介绍了两公司大豆蛋白废水的水质水量和性质特征,分析工程的工艺设计和调试运行状况.对大豆蛋白和屠宰废水的处理,采用混和处理的总体工艺,理论研究和运行实践表明,混和处理利于均衡生物处理营养,优化厌氧处理工艺型式及参数.污泥培养时,尽快从间歇运行变为连续运行,利于基质和污泥的混和接触,促进油脂和脂肪酸的降解,防止油和脂肪酸的积累及其抑制作用,防止油脂包覆污泥,造成污泥漂浮流失.     

A simple,rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria

The polymorphic information content (PIC) and the degree of heterozygosity of several polymorphic systems within the phenylalanine hydroxylase (PAH) gene were determined in 85 European Caucasian and 19 Chinese phenylketonuria (PKU) kindreds. The first system examined, a short tandem repeat (STR), had a PIC of 80 and 73 per cent in these Caucasian and Chinese samples, respectively. The degree of heterozygosity actually observed for this system was 81 and 64 per cent in the Caucasian and Chinese PKU families, respectively. Through the addition of a second polymorphism based on a variable number of tandem repeats (VNTR), the PIC was increased to 90 per cent in Caucasians, but only to 75 per cent in Chinese. The degree of heterozygosity observed for this combination was 94 per cent in European PKU families and 67 per cent in Chinese PKU families. The further addition of an Xmnl RFLP increased both the PIC and the level of heterozygosity in Caucasians to 95 per cent, but did not change either of these measures in Chinese. The combined use of these three polymorphisms significantly increases the informativity of prenatal diagnostic and carrier screening procedures in both Caucasian and Chinese PKU kindreds. Furthermore, since each of these polymorphisms can be studied by PCR-based methods, these new tests can be performed more quickly and easily than previous Southern-based procedures.     

对苯二甲酸复合降解生产单细胞蛋白的研究

研究通过降解对苯二甲酸的酵母和细菌的复合处理,使TA的降解率达到95%以上,并生产了单细胞蛋白。该单细胞蛋白营养价值高,经急性和遗传毒性试验表明属实际无毒类,并不具遗传毒性,是优良的单细胞蛋白。     

First-trimester maternal serum schwangerschafts protein 1 (SP1) in pregnancies associated with chromosomal anomalies

The relationship between first-trimester maternal serum Schwangerschafts protein 1 (SP1) and the karyotype of the pregnancy was examined in 692 women who underwent chorionic villus biopsy at 6–12 weeks. There were 30 pregnancies with abnormal karyotypes, consisting of 14 Down's syndrome (DS), eight trisomy 18, and eight other anomalies, two of which were mosaics. The normal ranges and medians for gestation were defined from the 662 cases in which the karyotype was normal. The median SP1 (0·5 MOM) of the abnormal group was significantly lower than that of the normal group (10 MOM). This relationship was maintained for the DS pregnancies (0·4 MOM) and for anomalies other than trisomy 18 (0·43 MOM) but not trisomy 18 (1·1 MOM). It is possible that the use of SP1 as a screening test for chromosome anomalies in the first trimester could have a 43 per cent detection rate for a 5 per cent false-positive rate.