subtilis 中文意思是什麼

subtilis 解釋
精細的,微薄的,敏銳的
  1. Ability of disintegrating amylum of b. subtilis hy - 02 producing - amylase

    澱粉酶的枯草芽胞桿菌分解澱粉的能力
  2. Optimization of one isolate bacillus subtilis

    一株枯草芽孢桿菌發酵培養基的優化
  3. Optimization on production conditions of fibrinolysin by bacillus subtilis sy

    豆豉纖溶酶產生菌的產酶條件優化
  4. 6 - phosphogluconate dehydrogenase ( 6 - pgadase, ec 1. 1. 1. 44 ) was isolated by homogenate, ammunium sulfate fractionation, deae - sepharose chromatography, blue - sepharose affinity chromatography and gel filtration with sephadex g - 200 from bacillus subtilis, and some properties of the enzyme had been studied. a 113. 8 - fold purification was obtained with a 8. 2 % yield. the purified enzyme moved as a single electrophoretic band in page

    將枯草芽孢桿菌超聲波破壁后的粗提取物進行分段鹽析、 deae - sepharose陰離子交換柱層析， blue - sepharosecl - 6b特異結合柱層析和sephadexg - 200凝膠過濾等純化步驟，得到聚丙烯酰胺凝膠電泳為單一蛋白區帶，比活為1 . 46u mg的酶制劑。
  5. The algorithm has been trained and tested on bacillus subtilis promoter dataset by the jackknife method

    對實際數據集進行的刀切法測試驗證了演算法的有效性。
  6. Used as 1. 1094 strain of bacillus subtilis as researched material, the structural genes of biotin operon ( bio operon ) were cloned, and its sequence were engineered

    本研究以枯草桿菌asl . 1094菌株為研究材料，克隆了生物素操縱子基因，並對基因序列進行改造。
  7. Used the genomic dna extracted by low melting - point agarose embedding method as pcr template, the full length of structural genes of bacillus subtilis bio operon were gained by long pcr method

    將該方法提取的基因組dna稀釋100倍作為模板，採用長距離pcr方法，獲得了枯草桿菌生物素操縱子基因全長。
  8. Effect of agitation rate on batch alkaline pectate lyases fermentation by bacillus subtilis

    分批發酵堿性果膠裂解酶的影響
  9. Promoting action of pilose autler for b. subtilis

    鹿茸對枯草桿菌的促菌作用
  10. The results showed : protamine could inhibit the growth of " bacillus subtilis " without destroying the cellular wall and significantly inhibit the activities of succinate dehydrogenase and malata dehydrogenase

    試驗結果表明：鯉魚魚精蛋白對枯草芽袍桿菌具有較強的抑制作用，但對枯草芽抱桿菌細胞壁不產生破壞作用；對黑曲?胞內的琥珀酸脫氫酶和蘋果酸脫氫酶的活性具有明顯的抑制作用。
  11. In order to investigate the antibacterial mechanism of protamine, the effect of protamine on the growth of " bacillus subtilis " and the activities of succinate dehydrogenase ( sdh ) and malata dehydrogenase ( mdh ) in cells of " aspergillus niger " was studied

    通過鯉魚魚精蛋白對枯草芽抱桿菌生長的影響及對黑曲?胞內的琥珀酸脫氫酶（ sdh ）和蘋果酸脫氫酶（ mdh ）活性影響的研究，探討鯉魚魚精蛋白的抑菌機理。
  12. By transformation with the genes. plant disease biocontrol bacteria bacillus subtil is aplls and b. megaterium ap25 were isolated from wheat field soils collected from south australia and tai an. enzyme activity analysis on chitin agar and abp media showed that b. subtilis aplls secreted chitinase and b. megaterium ap25 secreted endoglucanase, respectively

    測序后在genebank上進行序列比較，該基因片段同編號為2634966的枯草芽孢桿菌全序列的2599451到2812870 （功能未知）有85的同源性，但同已發表的13種幾丁質酶的基因（包括枯草芽孢桿菌幾丁質酶基因）的同源性很低，只有30 。
  13. In order to express alkaline protease gene ( ap gene ) in bacillus subtil is, the recombinant expression plasmid was constructed. this plasmid contains a promoter bp53, also from b. pumilus un - 31 - c - 42, ap gene and the shuttle vector psugv4. after introduced into b. subtilis wb600, the transformants displayed the hydrolyzed zone on milk plate

    將來自短小芽抱桿菌un一31一c礴2的基因啟動子（ bp53片段）和脫毛蛋白酶全基因（ ap ）進行融合，然後將重組基因（命名為bpap ）插入到大腸桿菌-枯草桿菌穿梭質粒載體psugv4中，構建成表達質粒psu一bpap 。
  14. The results showed that the extract by etoac presented a significant effect on staphylococcus aureau 、 bacillus cereus 、 bacillus megateriurn 、 proteus species, corynebacterium pekinense 、 trichoderma viride and aspergillus flavus all of which belonged to bacteria ; the extract by n - buoh presented significant inhibitory effect on bacillus mesentericus, bacillus subtilis 、 proteus species 、 bacterium prodigious, trichoderma viride and aspergillus flavus all of which belonged to bacterium ; the inhibitory effect become stronger and stronger with the extract concentration increaseing and the water phase of the extract did not present any antimicrobial effects

    結果表明，乙酸乙酯萃取物對細菌中的金黃色葡萄球菌、蠟狀芽孢桿菌、變形桿菌、巨大芽孢桿菌、北京棒狀桿菌和黴菌中的綠色木霉、黃麴黴有明顯的抑菌作用；正丁醇萃取物對細菌中的馬鈴薯芽孢桿菌、變形桿菌、枯草芽孢桿菌、靈桿菌和黴菌中的綠色木霉以及黃麴黴有明顯的抑菌作用，且提取物的抑菌作用隨濃度增大而增強，而水相則沒有抑菌活性。
  15. Experimental results indicated that there really were biosurfactant - producing bacteria and bacillus subtilis were the dominant biosurfactant - producing bacteria during composting

    實驗結果表明，堆肥過程中的確存在產生物表面活性劑的細菌，枯草芽孢桿菌是其主要菌之一。
  16. Extracts of 10 selected chinese herb medicines ( rhizoma coptidis, cortex phellodendri, radix scutellariae, fructus forsythiae, cortex magnoliae officinails, radix glycytthizae, folium artemisiae argyi, ligustici chuanxiong rhizoma, flos lonicerae, fructus schisandrae ) were tested in vitro against six different microorganisms [ bacteria ( staphylococcus aureus, escherichia coli and bacillus subtilis ), yeast ( saccharomyces cerevisiae ) and find ( aspergillus flavu and trichoderma viride )

    摘要本文選用黃連、黃柏、黃芩、連翹、厚樸、甘草、艾葉、川芎、金銀花及五味子十味中草藥水提液，對金黃色葡萄球菌、大腸桿菌、枯草芽孢桿菌、啤酒酵母、黃麴黴及綠色木霉這六種菌進行了體外抗菌試驗。
  17. The expression of oligo - 1, 6 - glucosidase from bacillus subtilis in pichia pastoris

    基因在畢赤酵母中的表達及酶學性質研究
  18. Based on the a - amylase - catalyzed hydrolysis of starch, pqci method has been developed to monitor the growth process of bacillus subtilis and the variation of the a - amylase activity during the growth. bacteria growth equations were derived based on the kinetics of the enzyme - catalyzed hydrolysis of starch

    將pqci技術應用於對枯草桿菌生長的研究，並且基於-澱粉酶對水溶性澱粉的酶促反應，推導出了枯草桿菌的pqci生長模型，包括諧振頻率、動態電阻和動態電感模型。
  19. A novel heparinase - producing strain was screened and isolated from siol samples. the strain was identified as bacillus subtilis, by testing physiological - biochemical and morphologic characteristics. we name it lx - 10

    以枯草芽孢桿菌為對照，並輔以大腸桿菌，經形態觀察和生理生化實驗，初步鑒定該菌株為枯草芽孢桿菌（ bacillussubtilis ） 。
  20. Besides, vgb gene expression also increased the chitinase secretion. in order to make the vitreoscilla hemoglobin gene express in bacillus subtilis, an inducible promoter ( levansucrase ) was cloned from b. subtilis wb600 and ligated with a promoter - less vgb gene. the resulted gene is called sacvgb and was demonstrated to express in e, coli by sds - page and carbon monoxide binding assay

    由於vgb基因啟動子不能在枯草桿菌中啟動表達，因此，根據已發表的果聚糖蔗糖酶基因（ sacb ）序列設計引物，從枯草桿菌wb600總dna中擴增出該基因的啟動子片段，然後將其與vgb基因編碼區及終止子序列相連，成功地組建了sacvgb融合基因。
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