黑麴黴 的英文怎麼說

Studies on the xylanase producer aspergillus niger

黑麴黴產木聚糖酶的研究

Purification and some properties of tannase from aspergillus niger

黑麴黴單寧酶的純化及部分性質研究

Study on the culture conditions of aspergillus to produce cellulase

黑麴黴產纖維素酶液體發酵條件的研究

Purification and properties of the cellulase from aspergillus niger

飼用黑麴黴纖維素酶的純化及酶學特性的研究

Studies on screening of strains of producing phytase and the conditions of producing phytase the strains of producing phytase could be identified by the hydrolysis bound in differential medium. aspergillus niger an010001 secreting phytase was isolated by screening and second screening. the conditions of producing phytase was studied

植酸酶菌株的篩選及產酶條件的研究本項研究利用植酸酶的菌株能在篩選培養基上形成水解透明圈的特點而進行鑒定，通過初篩和復篩，得到一株產植酸酶較高的黑麴黴（ aspergillusniger ） an00101菌株。

The principle and method for enzymatic synthesis of gallic acid, isolation and selection of the aspergillus niger strains, characteristics of this biotechnology, products quality of gallic acid and the uses in domestic food and pharmaceutical industries are briefly introduced

摘要概述了黑麴黴單寧酶酶法轉化五倍子單寧酸生產沒食子酸的原理和方法、酶源菌種的分離和選育、工藝技術的特點、產品質量規格及在國內食品、醫藥行業相關部門的應用等。

The results showed aspergillus niger bn was the optimal fungus, and the productive rate of gutta - perch increased 13. 3 %

結果表明，黑麴黴bn易於分解杜仲葉，且經其發酵處理后膠得率可提高13 . 3 % 。

Interspecific protoplast fusion between aspergillus terreus t - 730, an itaconic acid producer, and aspergillus niger ni - 5k, a glucoamylase producer, was done to breed new mold producing itaconic acid from starch. the ni - 5 strain was induced with antibiotic - a, which became a drugresistant strain ni - 5k

選擇衣康酸高產菌株犧土麴黴aspergillusterreust - 730和檸檬酸高產菌株黑麴黴aspergillusnigerni - 5 ，以抗菌素a對黑麴黴ni - 5進行誘導培育，形成遺傳穩定的抗藥性菌株ni - 5k 。

At present, most of lactases used in industry production come from kluyveromyces, aspergillus niger and aspergillus oryzae

目前，工業生產中使用的乳糖酶主要來源於乳酸克魯維斯酵母菌、黑麴黴和米麴黴。

Breeding of asperillus niger with high production of acid proteinase

高產酸性蛋白酶黑麴黴菌種選育

Two novel cellulases were identified and isolated to homogeneity from a commercial aspergillus niger cellulase preparation. one was an endo - l, 4 - - glucanase ( ec

本文是關于黑麴黴（ aspergillusniger ）中兩種纖維素酶的分離純化與表徵及其動力學作用機制的研究。

Purification and characterization of phytase from a. niger an 01001 a. niger an01001 was inoculated on solid media and cultivated at 30 for 5 days. proteins were extracted from solid - state fermentation with 50mm acetate buffer ( ph5. 5 ). the molecule weight of the phytase protein was determined as about 78kd by sds - page. the purification procedures include ammonium sulfate precipitation, deae - cellulose ion - exchange chromatography, gel electrophoresis and electroelution

3 .植酸酶的分離純化及其性質研究黑麴黴ano1001經固體發酵，用緩沖液抽提后，經硫酸按沉澱， deae一纖維素離子交換層析，聚丙烯酞胺凝膠電泳和電洗脫等純化步驟獲得的植酸酶，用sds一page檢測為一條均一譜帶，其分子量約為78kd 。

Purification and properties of an endo - - glucanase from a commercial preparation of aspergillus niger

黑麴黴產纖維素酶系中內切酶的純化和性質

Characteristic of respective components from cellulase system induced by aspergillus niger and condition of enzymolysis

黑麴黴產纖維素酶系各組分特性及酶解條件

In the ht medium with 2 % starch, after the strain nust03 had been culturing on a rotary shaker at 28, 220r / min for 96 hours, the fermentation can restrain the growth of a. niger

Nusto3菌株在含有2的可溶性澱粉的ht培養基上，搖床（ 28 ， 200r min ）培養96小時，發酵液對黑麴黴有抑制作用。

Study on property of extracellular pectinase from aspergulus niger

黑麴黴胞外果膠酶特性的研究

Primary study on pectinase processing condition by liquid - state fermentation with aspergillus niger

黑麴黴液態發酵生產果膠酶的工藝條件初探

Study on the technologies of liquid - state fermentation for producing pectinase with aspergillus niger

黑麴黴液態發酵生產果膠酶的工藝條件初探

The anti - pathogenic activities of capsaicin, which was extracted from the chosen hot pepper, against three pathogenic bacteria and seven pathogenic fungi were evaluated

摘要從紅辣椒中提取的辣椒堿對金黃色葡萄球菌、大腸桿菌、枯草芽孢桿菌這3種常見的病原細菌及黑麴黴、啤酒酵母等7種病原真菌進行拮抗試驗。

Benzyl chloride were used for extracting genomic dna of aspergillus. niger 14, about 1. 5kb specific fragment was obtained from genomic dna of aspergillus. niger 14 by pcr amplification with primers ( forward primer5 " ataggcatcatgggcgtctct3 " reverse - primer5 " cagctaagcaaaacactccgc 3 designed according to the known sequences of the phytase gene in the gene bank and pyrobest ? dna polymerase, after ligated with pmd18 - tvector, transformated into e. colidh5a competent cell successfully. 3. nucleotide sequence analysis of the cloned fragment revealed the presence of the whole phya gene in pcr product

用氯化芐法提取了aspergillus . niger14 ~ #基因組dna ，根據genebank中已知的黑麴黴植酸酶基因序列設計出一對特異性引物（上游引物： 5 ataggcatcatgggcgtctc3下游引物： 5 cagctaagcaaaacactccgc3 ） ，採用pyrobest ~ （ tm ） dnapolymerase （高保真dna聚合酶） ，通過pcr方法從aspergillus . niger14 ~ #基因組dna中擴增出了預期的1 . 5kb左右的特異性產物，將其與pmd18 - tvector連接后，轉化e . colidh5菌株的感受態細胞，經質粒抽提、酶切鑒定，確認該目的產物已得到成功克隆。