| 1. | Study on characters of neutral protease from aspergillus or yzae
米曲霉中性蛋白酶特性的研究 |
| 2. | Study on soybean isoflavone - glycosidase fermented by aspergillus oryzae
米曲霉产大豆异黄酮糖苷酶发酵条件的研究 |
| 3. | Suitable conditions for the production of neutral proteinase by aspengillus oryzae
米曲霉产中性蛋白酶的适宜条件 |
| 4. | Optimizing the medium of asperillus oryzae strains for prdoucing fibrinolytic enzyme
米曲霉发酵产纤溶酶培养基的优化 |
| 5. | Study on rejuvenation and preservation of aspergillus oryzae xi - 3 , a neutral protease producing strain
3米曲霉菌株的保藏与复壮 |
| 6. | Analysis of kojic acid in aspergillus oryzae ferment by ion - pair reversed - phase high performance liquid chromatography
离子对高效液相色谱法分析米曲霉发酵液中的曲酸 |
| 7. | At present , most of lactases used in industry production come from kluyveromyces , aspergillus niger and aspergillus oryzae
目前，工业生产中使用的乳糖酶主要来源于乳酸克鲁维斯酵母菌、黑曲霉和米曲霉。 |
| 8. | Aspergillus oryzae , a kind of filamentous fungus , has been widely used in industrial production . so far , we do n ' t know so much about its transcription mechanism
米曲霉aspergillusoryzae是一种广泛应用于工业的丝状真菌，但现在人们对它的转录调控机制还知之甚少。 |
| 9. | The gene encoding tannase was amplified from the total dna of aspergillus oryzae by pcr and was expressed in e . coli and pichia pastoris . the gene was insered in the expression plasmid pse380 . the recombinant plasmid pse380 - tan was transformed into e . coli strains dh5a , top10 , bl21 ( de3 )
本论文以米曲霉aspergillusoryzae的总dna为模板， pcr扩增了单宁酶基因( tan ) ，并分别尝试了利用大肠杆菌( escherichiacoli )和巴斯德毕赤酵母( pichiapastoris )进行表达。 |
| 10. | 3 . the cloning of a - amylase gene : the methods of shotgun , pcr and rt - pcr were selected to clone a - amylase genes from bacillus subtilis hn503 , xanthomonas campestris pv . campestris 8004 and aspergillus oryzae , hn504 the recombinant plasmid with cloned gene was designated as phn504 , phn503 and phn8004
本研究分别选用了鸟枪克隆法、 pcr和rt - pcr克隆法，成功地克隆到枯草芽胞杆菌( bacillussubtilis ) hn503 、野油菜黄单胞菌( xanthomonascampestrispvcampestris ) 8004和米曲霉( aspergillus口尽留‘ ) hn504的价淀粉酶基因。 |
