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一株降解生木薯淀粉的曲霉菌株的筛选、鉴定及其淀粉降解特性
引用本文:宋贤冲,田会会,陈国利,许剑,樊宪伟,李有志. 一株降解生木薯淀粉的曲霉菌株的筛选、鉴定及其淀粉降解特性[J]. 广西农业生物科学, 2011, 30(5): 596-602
作者姓名:宋贤冲  田会会  陈国利  许剑  樊宪伟  李有志
作者单位:亚热带农业生物资源保护与利用国家重点实验室,南宁,530005
基金项目:国家科技部科技人员服务企业行动项目“酶工程法生产魔芋甘露低聚糖产业化科技服务示范(2009GJE10020)”资助致谢 感谢广西大学冯家勋老师惠赠的生淀粉底物,感谢广西大学生命科学与技术学院庞宗文老师、韦宇拓老师、吴磊同学和梁甲元同学在高效液相色谱分析中给予的帮助和指导,感谢广西大学材料与工程学院温静娴和于梅花老师在扫描电镜观察上提供的帮助,感谢对本研究成稿做出贡献的所有老师和同学!
摘    要:
本研究利用以生木薯淀粉为唯一碳源的筛选培养基,从腐烂木薯渣中分离筛选出一株可以降解生木薯淀粉的真菌菌株RSDF-7。根据RSDF-7形态和18SrDNA与28SrDNA之间的内转录间隔区(internal transcribed spacer,ITS)序列分析的结果,初步认定该菌株为曲霉属。菌株RSDF-7的粗酶液对多种不同的生淀粉底物均有水解效果;在以大米和玉米淀粉为底物时,其生淀粉分解活力比较高,分别为42%和40%。菌株RSDF-7的粗酶液具有良好的低pH稳定性,对生木薯淀粉的最适作用温度为50℃,最适作用pH为4.5。在30min的吸附后,RSDF-7的粗酶液对生木薯淀粉的吸附力高达60%。使用HPLC对粗酶液的酶解产物进行检测,结果发现酶解产物中仅存在葡萄糖,表明菌株RSDF-7所产的生淀粉降解酶主要为糖化酶。扫描电镜观察结果发现,经RSDF-7粗酶液酶解后的生木薯粉颗粒破裂,形成空洞,说明RSDF-7粗酶液对生淀粉有较强的水解作用。可以预见,经纯化后的曲霉菌株RSDF-7生淀粉酶将来可以用于基于酶解的木薯淀粉转化。

关 键 词:生木薯淀粉  筛选  糖化酶  曲霉

Screening and Identification of a Raw Cassava Starch-hydrolyzing Aspergillus Strain and Its Characteristics of Starch Degradation
Song Xianchong,Tian Huihui,Chen Guoli,Xu Jian,Fan Xianwei,Li Youzhi. Screening and Identification of a Raw Cassava Starch-hydrolyzing Aspergillus Strain and Its Characteristics of Starch Degradation[J]. Journal of Guangxi Agricultural and Biological Science, 2011, 30(5): 596-602
Authors:Song Xianchong  Tian Huihui  Chen Guoli  Xu Jian  Fan Xianwei  Li Youzhi
Affiliation:1,2* 1 State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources,Nanning,530005;2 College of Life Science and Technology,Guangxi University,Nanning,530005
Abstract:
A raw cassava starch-hydrolyzing fungal,numbered as RSDF-7,was isolated and screened from the decayed cassava dreg using the screening medium with raw cassava starch as the sole carbon resource.The crude enzyme of strain RSDF-7 showed the better stability within a lower range of pHs.The optimum temperature for digestion of raw starch was 50℃,and the optimum pH was at 4.5.The crude enzyme from the culture of RSDF-7 could hydrolyze several different raw starch substrate,the values of raw starch-degrading ability were higher,with about 42% and 40% using corn and rice starch as the substrate,respectively.Analysis of the morphology and internal transcribed spacer region sequence between 18S rDNA and 28S rDNA indicated that the RSDF-7 belongs to Aspergillus sp..The absorption rate of raw cassava starch by RSDF-7 was about 60% after 30 min adsorption.Assay of high performance liquid chromatography indicated that the enzymatic product of raw cassava starch by the crude enzyme from RSDF-7 was only glucose,suggesting that the crude enzyme produced by RSDF-7 is starch-digesting glucoamylase.The scanning electron microscope revealed that the raw cassava starch granules ruptured and presented larger cavities after digestion treatment with the crude enzyme,indicating that the enzyme has a stronger ability to digest the raw starch.It was expected that enzyme from Aspergillus strain RSDF-7 after purification can be used in enzymatic-based digestion conversation of cassava starch in future.
Keywords:Raw cassava starch  Screening  Glucoamylase  Aspergillus
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