[1]张荣奎,贺淹才,刘爱花,等.土壤产几丁质酶菌株的筛选鉴定及产酶条件[J].华侨大学学报(自然科学版),2007,28(2):178-181.[doi:10.3969/j.issn.1000-5013.2007.02.018]
 ZHANG Rong-kui,HE Yan-cai,LIU Ai-hua,et al.Isolation and Identification of a Chitinase-Producing Bacterium in Soil and Studies on the Chitinase Fermentation Condition[J].Journal of Huaqiao University(Natural Science),2007,28(2):178-181.[doi:10.3969/j.issn.1000-5013.2007.02.018]
点击复制

土壤产几丁质酶菌株的筛选鉴定及产酶条件()
分享到:

《华侨大学学报(自然科学版)》[ISSN:1000-5013/CN:35-1079/N]

卷:
第28卷
期数:
2007年第2期
页码:
178-181
栏目:
出版日期:
2007-04-20

文章信息/Info

Title:
Isolation and Identification of a Chitinase-Producing Bacterium in Soil and Studies on the Chitinase Fermentation Condition
文章编号:
1000-5013(2007)02-0178-04
作者:
张荣奎贺淹才刘爱花魏巍李红然
华侨大学材料科学与工程学院; 华侨大学材料科学与工程学院 福建泉州362021; 福建泉州362021
Author(s):
ZHANG Rong-kui HE Yan-cai LIU Ai-hua WEI Wei LI Hong-ran
College of Material Science and Engineering, Huaqiao University, Quanzhou 362021, China
关键词:
嗜麦芽窄食单胞菌 几丁质酶 16SrDNA鉴定 发酵条件
Keywords:
Stenotrophomonas maltophilia chitinase 16S rDNA identification fermentation conditions
分类号:
S154.3
DOI:
10.3969/j.issn.1000-5013.2007.02.018
文献标志码:
A
摘要:
利用几丁质为碳源,从土壤中筛选出3株产几丁质酶菌株,其中酶活最高的为一株革兰氏阴性菌.对该菌株应用16S rDNA法进行鉴定,结果为嗜麦芽窄食单胞菌(Stenotrophomonas maltophilia).通过单因素优化法和均匀设计法实验,结果表明,以质量分数0.5%的胶体几丁质为碳源,质量分数1.0%的蛋白胨为氮源,及30℃和pH值为7.2,发酵60 h的条件是菌株的最合适产酶条件.此时,胞外几丁质酶酶活力最高.
Abstract:
Three strains with chitinase activity were isolated from soil.The strain with the maximum enzyme activity level was a Gram negative bacterium which was identified as Stenotrophomonas maltophilia chitinase strain by 16S rDNA method.The study on the synthetic conditions for the chitinase by single factor optimization method and uniform design method showed that the optimal synthesis conditions for chitinase was as follows: the strain was cultured for 60 hours in a basic medium(pH 7.2,30 ℃) added by 0.5% chitin and 1.0% peptone.

参考文献/References:

[1] BROGLIE K E. Chitinase and plant protection [J]. Rev Plant Pathol, 1993(2):411-421.
[2] 李力, 黄胜元, 关雄. 产几丁质酶的苏云金杆菌菌株筛选及酶合成条件研究 [J]. 中国病毒学, 2000, (51):94-97.
[3] CHANG Yu-cheng, YANG Chiyea, LI Chin. Identification of Bacillus sp, Escherichia coli, Salmonella sp, Staphylococcus sp and Vibrio sp with 16Sribosomal DNA-based oligonucleotide array hybridization [J]. International Journal of Food Microbiology, 2006, (2):131-137.doi:10.1016/j.ijfoodmicro.2005.04.028.
[4] 张龙翔, 张庭芳, 李令媛. 生化实验技术 [M]. 北京:高等教育出版社, 1997.111-116.
[5] MOORE E R, KRUGER A S, HAUBEN L. 16SrRNA gene sequence analyses and inter-and intrageneric relationships of Xanthomonas species and Stenotrophomonas maltophilia [J]. FEMS Microbiology Letters, 1997(2):145-153.doi:10.1111/j.1574-6968.1997.tb12563.x.
[6] MIYAJI T, OTTA Y, SHIBATA T. Purification and characterization of extracellular alkaline serine protease from Stenotrophomonas maltophilia strain S-1 [J]. Letters in Applied Microbiology, 2005(3):253-257.doi:10.1111/j.1472-765X.2005.01750.x.
[7] MADHAVAP N K, BAIJU T V, SANDHYA C. Process optimization for antifungal chitinase production by Trichoderma harzianum [J]. Process Biochemistry, 2004.1583-1590.doi:10.1016/S0032-9592(03)00282-6.
[8] NAWANI N N, KAPADNIS B P. Optimization of chitinase production using statistics based experimental designs [J]. Process Biochemistry, 2005.651-660.doi:10.1016/j.procbio.2004.01.048.

相似文献/References:

[1]施腾鑫,刘嘉,贺淹才.黏质沙雷氏菌产几丁质酶的发酵工艺优化[J].华侨大学学报(自然科学版),2010,31(6):667.[doi:10.11830/ISSN.1000-5013.2010.06.0667]
 SHI Teng-xin,LIU Jia,HE Yan-cai.Culture Parameter Optimization of Chitinase Production by Serratia marcescens[J].Journal of Huaqiao University(Natural Science),2010,31(2):667.[doi:10.11830/ISSN.1000-5013.2010.06.0667]
[2]施腾鑫,贺淹才,刘嘉,等.黏质沙雷氏菌产几丁质酶二步发酵工艺的优化[J].华侨大学学报(自然科学版),2011,32(1):67.[doi:10.11830/ISSN.1000-5013.2011.01.0067]
 SHI Teng-xin,HE Yan-cai,LIU Jia,et al.Optimization of Chitinase Production by Serratia marcescens with Two-Step Fermentation[J].Journal of Huaqiao University(Natural Science),2011,32(2):67.[doi:10.11830/ISSN.1000-5013.2011.01.0067]

备注/Memo

备注/Memo:
福建省自然科学基金资助项目(C04010011)
更新日期/Last Update: 2014-03-23