摘要
【目的】本研究的目的是优化Pseudoalteromonas sp.AJ5菌株的培养条件使之产生高活性的胞外κ-卡拉胶酶。【方法】通过富集培养技术从刺参肠道分离出一株卡拉胶降解菌AJ5,该菌株能利用卡拉胶作为惟一碳源和能源。依据形态学和生理学特征及16SrRNA基因序列分析,将该菌株鉴定为假交替单胞菌属(Pseudoalteromonas)。通过单因素试验和正交试验对Pseudoalteromonas sp.AJ5菌株产胞外κ-卡拉胶酶的培养条件进行了优化。【结果】单因素试验结果表明,Pseudoalteromonas sp.AJ5菌株的最佳培养条件为250mL三角瓶装入75mL发酵培养基、摇床转速150r/min、接种量7%、pH8.0。单因素试验和正交试验结果显示该菌株的最佳培养基组成为κ-卡拉胶1g/L、牛肉膏2g/L、NaCl20g/L、K2HPO4·3H2O1g/L、MgSO4·7H2O0.5g/L、MnCl2·4H2O0.2g/L、FePO4·4H2O0.01g/L;培养温度为28℃,培养时间为28h。【结论】Pseudoalteromonas sp.AJ5菌株分泌胞外κ-卡拉胶酶,在最佳培养条件下,该菌株的κ-卡拉胶酶活力比优化前提高了4倍。
[Objectives] To optimize the culture conditions of Pseudoalteromonas sp. AJ5 for a higher production of extracellular κ-carrageenase. [Methods] A κ-carrageenan-degrading bacterium AJ5, capable of utilizing κ-carrageenan as sole source of carbon and energy, was isolated from the intestine of holothurian Apostichopus japonicus by enrichment culture technique. The strain was identified as the genus Pseudoalteromonas sp. according to its morphological and physiological characterization and 16S rRNA gene analysis. Culture conditions for the bacterium were standardized for the maximal productivity of the extracellular κ-carrageenase by the single factor and orthogonal tests. [Results] According to the single factor test, the optimal culture conditions were: 75 mL medium in 250 mL Erlenmeyer flask, shaking speed of 150 r/min, inoculum's volume 7%, and pH 8.0. Based on the single factor and orthogonal tests the optimal medium components were: κ-carrageenan (1 g/L), beef extract (2 g/L ), NaCI (2O g/L), K2HPO4·3H2O (1 g/L), MgSO4·7H2O (0.5 g/L), MnCI2-4H2O (0.2 g/L), FePO4·4H2O (0.01 g/L), with the incubation temperature and time of 28℃ and 28 h. [Conclusions] Pseudoalteromonas sp. AJ5 secreted an extracellular κ-carrageenase. Under the optimal culture conditions, four-fold increase in κ-carrageenase activity was achieved as compared to the control.
出处
《微生物学报》
CAS
CSCD
北大核心
2008年第6期757-764,共8页
Acta Microbiologica Sinica
基金
国家自然科学基金(40506027)
农业部海洋水产增养殖学与生物技术重点开放实验室开放课题(K2006-12)~~