| 1. | Analysis of cellulose hydrolysis products in extremely low acids
纤维素超低酸水解产物的分析 |
| 2. | Acid hydrolyzed vegetable protein seasoning
酸水解植物蛋白调味液 |
| 3. | Surface active agents . anionic active matter stable to acid hydrolysis . determination of trace amounts
表面活性剂.阴离子活性物质对酸水解的稳定性.痕量成分的测定 |
| 4. | The content of levulinic acid in soy sauce , hydrolyzed vegetable protein ( hvp ) and caramel was determined
摘要对酱油、酸水解植物蛋白( hvp ) 、焦糖色素中乙酰丙酸的含量进行了测定。 |
| 5. | The content of levulinic acid was relatively lower in soy sauce and higher in hvp ( the maximum was 15 . 79 % )
其中，酱油中乙酰丙酸含量较低，酸水解植物蛋白中乙酰丙酸含量较多（最高含量为15 . 79 % ） ，而焦糖色素中也测出含有乙酰丙酸（最高含量达8 . 02 % ） 。 |
| 6. | The active agent was confirmed as oligosaccharide , mostly composed of glucose by pc , vc and acidhydrolysis . the active agent is stable between ph2 - 12 and below 90c
通过纸层析（ pc ）和柱层析（ vc ）分析，活性组分酸水解分析初步证实了其组分为葡萄糖为主要成分组成的寡糖类物质。 |
| 7. | Phytases are hydrolytic enzymes that initiate the release of phosphate from phytate , the major phosphorus ( p ) form in animal feeds of plant origin . phytases are found naturally in microorganisms and plants
植酸是植物性饲料中磷的主要贮存形式，植酸酶是一种能将植酸水解并释放出无机磷的酶，它广泛存在于微生物与植物中。 |
| 8. | The paper deals with the isolation and identification of a creatinase - producing bacterium from soil , the conditions for production of creatinase , purification methods of creatinase and the purified enzyme characteristics
1 、产肌酸水解酶微生物的分离及鉴定本研究用恒化培养的方法从土壤中富集微生物，然后再用平板划线分离。 |
| 9. | Methods : in the present experiment , acid dehydroxy amino acid analysis and isoelectric focusing in polyacylamide gels were used and the amino acid composition and isoelectric point of porcine platelet - derived growth factor were studied
方法：用酸水解及聚丙烯酰胺凝胶等电聚焦的方法测定猪血小板衍生生长因子的氨基酸含量、组成成分和等电点。 |
| 10. | Then enzyme was purified with a deae - cellulose ( 5 . 5x50cm ) column , a toyopearl hw - 65 ( 5 . 5 x 50cm ) column and a sephadex g - 200 ( 5 . 5 x 80cm ) column . finally , the enzyme was purified for 10 folds with the recovery of 17 . 4 % . page showed a single band for the purified creatinase
3 、肌酸水解酶的提纯酶在硫酸铵饱和度为40 80之间完全沉淀，先后经过deae - cellulose离子层析柱、 toyopearlhw - 65疏水层析柱、 sephadexg - 200分子筛层析柱层析，最终使酶提纯10倍，最终得率为17 . 4 。 |
