中国烟草科学
中國煙草科學
중국연초과학
CHINESE TOBACCO SCIENCE
2013年
2期
41-44
,共4页
战徊旭%申莉莉%韩志忠%杨金广%钱玉梅%王盼%王凤龙
戰佪旭%申莉莉%韓誌忠%楊金廣%錢玉梅%王盼%王鳳龍
전회욱%신리리%한지충%양금엄%전옥매%왕반%왕봉룡
TMV%拮抗细菌%培养基优化
TMV%拮抗細菌%培養基優化
TMV%길항세균%배양기우화
TMV%antagonistic bacteria%medium optimization
利用单因素试验结合正交试验的方法,以菌体生长量(OD600值)作为测定指标,对TMV拮抗细菌恶臭假单胞杆菌A3的培养基进行优化,系统研究了碳源、氮源、无机盐的发酵结果.试验结果表明,碳源为麦麸,氮源为酵母浸粉,无机盐为CaCl2、CoCl2、MgSO4、FeSO4、KH2PO4时有利于A3的生长.7因素3水平正交试验结果表明,培养基的最优组合为麦麸15 g,酵母浸粉15 g,CaCl22.5 g,CoCl20.5 g,MgSO40.8 g,FeSO40.5 g,KH2PO40.8 g,蒸馏水1000 mL,pH 7.0,在此条件下拮抗细菌活菌数可达3.234×1012 cfu/mL,比NB培养基中活菌数提高一个数量级.
利用單因素試驗結閤正交試驗的方法,以菌體生長量(OD600值)作為測定指標,對TMV拮抗細菌噁臭假單胞桿菌A3的培養基進行優化,繫統研究瞭碳源、氮源、無機鹽的髮酵結果.試驗結果錶明,碳源為麥麩,氮源為酵母浸粉,無機鹽為CaCl2、CoCl2、MgSO4、FeSO4、KH2PO4時有利于A3的生長.7因素3水平正交試驗結果錶明,培養基的最優組閤為麥麩15 g,酵母浸粉15 g,CaCl22.5 g,CoCl20.5 g,MgSO40.8 g,FeSO40.5 g,KH2PO40.8 g,蒸餾水1000 mL,pH 7.0,在此條件下拮抗細菌活菌數可達3.234×1012 cfu/mL,比NB培養基中活菌數提高一箇數量級.
이용단인소시험결합정교시험적방법,이균체생장량(OD600치)작위측정지표,대TMV길항세균악취가단포간균A3적배양기진행우화,계통연구료탄원、담원、무궤염적발효결과.시험결과표명,탄원위맥부,담원위효모침분,무궤염위CaCl2、CoCl2、MgSO4、FeSO4、KH2PO4시유리우A3적생장.7인소3수평정교시험결과표명,배양기적최우조합위맥부15 g,효모침분15 g,CaCl22.5 g,CoCl20.5 g,MgSO40.8 g,FeSO40.5 g,KH2PO40.8 g,증류수1000 mL,pH 7.0,재차조건하길항세균활균수가체3.234×1012 cfu/mL,비NB배양기중활균수제고일개수량급.
The experiments with one factor and orthogonal design were conducted to optimize medium of antagonistic bacteria A3 strain against TMV (Pseudomonas putida) with mass growth (OD600 value) as the index. A systematic study of carbon sources, nitrogen sources and inorganic chemicals was carried out. Carbon source“wheat bran”, nitrogen source“yeast extract powder”and inorganic chemical“CaCl2, CoCl2, MgSO4, FeSO4, KH2PO4”, were beneficial to the growth of A3. The results of L18(37) orthogonal tests showed that optimal medium menu included 15g wheat bran,15g yeast extract powder, 2.5g CaCl2, 0.5g CoCl2, 0.8g MgSO4, 0.5g FeSO4, 0.8g KH2PO4 and 1000mL distilled water, pH 7.0. The number of live bacteria could be 3.234×1012 cfu/mL in the optimized medium and the number increased by one orders of magnitude than original NB medium.