华芬酶在仔猪玉米-豆粕型日粮的应用研究

选用 32头体重在 15～ 18kg的杜大长三元杂交生长小猪 ,随机分成 4组 ,3个试验组在对照组日粮的基础上分别添加 0 0 8%、0 1%、0 12 %华芬酶 130 1,以观察其饲养效果。试验结果表明 :3个试验组的日增重 (g/d)分别为 6 30、5 2 0、5 2 5 ,比对照组 ( 4 5 0g/d)分别提高 4 0 %、15 5 5 %、16 6 6 % ,(P <0 0 1) ;料重比分别为 1 81、2 10、1 96 ,以添加 0 0 8%组的效果最好 ,比对照组提高 7 13% (P <0 0 5 )。     

cDNA Cloning and Sequence Analysis of Rice Sbel and Sbe3 Genes

Two starch-branching enzyme (SBE) in rice, is known to be a key enzyme in amylopectin biosynthesis. The cDNA of two SBE(starch-branching enzyme) genes SheI and Shed encoding SBE Ⅰ and SBE Ⅲ (two major isoforms in rice) were cloned by an improved RT-PCR technique, from a template cDNA libray, derived from the total mRNAs extracted from the immature seeds of a japonica rice Wuyunjing 7. DNA sequence analysis showed that the size of the cloned SheI and Shed cDNAs were 2490 and 2481 bp long, respectively, including their entire coding sequences. Comparison analysis indicated that the nucleotide sequence of She3 was the same as that of shed (Genbank Accession No. D16201) as reported previously. There were only four base-pairs difference,which resulted in changes of two deduced amino acids between the cloned She1 cDNA and the reported she1 (Genbank Accession No. D11082). The cloned SheI and Shed cDNAs make it possible to improve rice starch quality through genetic engineering.     

氯霉素全抗原合成及多克隆抗体的制备

用重氮化方法将氯霉素与牛血清白蛋白（BSA）和卵清蛋白（OVA）偶联，制备免疫抗原和包被抗原，用ELISA方法进行鉴定。将偶联抗原用弗氏佐剂乳化后免疫德国大白兔。制备多克隆抗体，并用硫酸铵沉淀法初步纯化。用亲和层析法进一步纯化。用所得抗体建立竞争酶联免疫吸附分析法（ELISA）用于氯霉素检测，最低检查限为0.3ng/mL。     

木聚糖酶产生菌的筛选及酶学性质研究

从实验室保藏的13株菌株中筛选到l株高产木聚糖酶菌株-黑曲霉2107,酶谱检测发现,该茵株产2种木聚糖酶X-1和X-2.X-1和X-2的最适反应温度都为50℃,并在30～50℃都较稳定.X-1的半失活温度50～55℃,X-2的半失活温度为55～60℃.X-1的最适pH约为5,pH 4～10较稳定;X-2的最适pH约为3和4之间,pH 2～5之间较稳定.各种金属离子对2种酶都有不同程度的抑制作用.     

漆酚热预聚漆研究（Ⅰ）──漆酚热预聚漆酶催化成膜

为了充分让漆酶在最后催化成膜中发挥作用，将生漆分离出漆酚和粗漆酶后，先将漆酚进行热预聚，再用粗漆酶配制成漆酚热预聚漆。试验结果表明：此法配制出的漆液，不仅能在漆酶催化下成膜，而且具有粗漆酶用量少、干燥性能好的特点。     

棉花纤维发育后期Mg2+,K+-ATP酶的活性分析

1989～1990年选用陆地棉(G.hirstum L.)北农1号品种和海岛棉(G.barbadenseL.)海7124品种为材料,对棉纤维发育后期的纤维素形成过程进行了研究。结果表明:①随着棉纤维的发育 Mg~(2+),K~+-ATP 酶活性逐渐下降。②Mg~(2+),K~+-ATP 酶活性的最适 pH 值为6.5。Mg~(2+),K~+ATP 酶活性随[Mg~(2+)],[K~+]和[NADH]/[NAD~+]的增大而变大。③Mg~(2+),K~+ATP 酶活性变化与还原性糖含量变化呈显著正相关(r=0.811~*),与纤维素含量变化呈极显著负相关(r=-0.900~(**))。④Mg~(2+),K~+-ATP 酶参与了纤维素的形成过程。