CN103937692B - 一株丝枝霉菌株及其生产β-葡萄糖苷酶的方法 - Google Patents
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Abstract
一株丝枝霉菌株及其生产β-葡萄糖苷酶的方法,属于食品生物技术领域。本发明提供一株新的可产β-葡萄糖苷酶的丝枝霉菌株,该丝枝霉菌株命名为丝枝霉(<i>Aphanocladium</i><i></i>sp<i>.</i>)SK34.001,保藏号为CCTCC?NO:M?2014090。本发明对β-葡萄糖苷酶产生菌丝枝霉进行斜面、种子、发酵三级培养;从发酵液中分离纯化得到β-葡萄糖苷酶酶粉。本发明提供的利用丝枝霉(<i>Aphanocladium</i><i></i>sp<i>.</i>)SK34.001生产β-葡萄糖苷酶的方法,其发酵工艺简单;酶易于提取;酶活高,酶性质稳定;可直接利用麸皮等废弃资源作为该菌株的培养基碳源,节省能源消耗,降低生产成本,具有广阔的市场应用前景。
Description
技术领域
本发明涉及一株丝枝霉菌株及其生产β-葡萄糖苷酶的方法,属于食品生物技术领域。
背景技术
β-葡萄糖苷酶(EC3.2.1.21),也称β-D-葡萄糖苷酶,它能够水解结合于底物末端非还原性的β-D-葡萄糖苷键,同时释放出葡萄糖和相应的配基。β-葡萄糖苷酶存在于自然界许多植物、昆虫、酵母、霉菌及细菌体内,它参与生物体的糖代谢,对维持生物体正常生理功能起着重要作用。
β-葡萄糖苷酶在自然界广泛分布,几乎在所有的生物体中都有存在,但来源不同,其性质各异。该酶对糖苷非糖部分的专一性不强,能水解许多β型的糖苷键。
β-葡萄糖苷酶除主要用于降解纤维素以外,还可应用于乳品工业来分解乳糖;催化葡萄糖发生转移反应和缩合反应合成功能性低聚糖,如低聚龙胆糖;作为风味酶应用于(果)酒、茶叶、果汁中起到增香或脱苦作用;另外,β-葡萄糖苷酶还可用来水解大豆异黄酮,制备高活性的大豆异黄酮苷元产品。
目前,国内外用于研究和制备β-葡萄糖苷酶的微生物主要有木霉属(Trichoderma)和曲霉属(Aspergillus)。研究表明,许多曲霉属是生产高活力β-葡萄糖苷酶的优良菌株,且被认为是不会产生毒素的纤维素酶产生菌,因而研究比较深入。迄今为止,还没有丝枝霉(Aphanocladium)作为β-葡萄糖苷酶产生菌的相关研究报道。
发明内容
本发明的目的是提供一种丝枝霉菌株及其生产β-葡萄糖苷酶的方法。
本发明的技术方案,一株丝枝霉菌株,是本发明人等先前从腐殖土壤样品中分离筛选得到的一株可以高产β-葡萄糖苷酶的丝枝霉菌株,分类命名为丝枝霉(Aphanocladiumsp.)SK34.001,其保藏号为CCTCCNO:M2014090,保藏单位为中国典型培养物保藏中心。
所述菌株的核糖体DNAITS序列如SEQIDNO:1所示。
所述丝枝霉菌株CCTCCNO:M2014090生产β-葡萄糖苷酶的方法,步骤如下:
(1)斜面培养:取丝枝霉菌株CCTCCNO:M2014090进行斜面培养,采用PDA培养基,各组分以g/L计:马铃薯200,葡萄糖20,琼脂15~20;自然pH,115℃下灭菌30min;培养温度为25~35℃,培养时间3~8天;
(2)种子培养:采用牛肉膏蛋白胨培养基,各组分以g/L计:牛肉膏2~5,胰蛋白胨5~8,氯化钠2~5,自然pH,121℃灭菌20min;在250mL三角瓶装液30~50mL,将步骤(1)所得的斜面培养液进行种子培养,摇瓶转速150~200rpm,培养温度25~35℃,培养时间18~24h;
(3)发酵培养:发酵培养基组分以g/L计:麸皮20~40,硫酸铵4~6,磷酸二氢钾2~3,硫酸镁0.3~0.5,氯化钙0.3~0.5,自然pH,121℃灭菌20min;步骤(2)所得的种子培养液按体积百分数2%~5%接种量接种于发酵培养基中,摇瓶转速150~200rpm,培养温度25~35℃,培养时间3~8天;
(4)β-葡萄糖苷酶酶粉制备:将步骤(3)制得的发酵液在5000~10000rpm离心10~30min或过滤去除菌体即得发酵上清液,经超滤除去盐和杂蛋白,再经硫酸铵沉淀、透析,最后将透析液进行冷冻干燥即得β-葡萄糖苷酶酶粉。
本发明中的β-葡萄糖苷酶活性,是通过使酶作用于对硝基苯-β-D-葡萄糖苷(pNPG),分解所生成的对硝基苯酚的量而测定。该酶的单位定义为每分钟生成1μmol对硝基苯酚的酶量。
本发明的有益效果:本发明为首次采用丝枝霉(Aphanocladium)作为β-葡萄糖苷酶的产生菌,该菌株培养方便,发酵工艺简单。其所产酶为胞外酶,易于提取,酶活高,酶性质稳定,可直接利用麸皮等废弃资源作为丝枝霉(Aphanocladium)的培养基碳源,节省能源消耗,降低生产成本,具有广阔的市场应用前景。
生物材料样品保藏:一株丝枝霉菌株,分类命名为丝枝霉(Aphanocladiumsp.)SK34.001,该菌株已于2014年3月14日保藏于中国典型培养物保藏中心,简称CCTCC,地址:中国武汉,武汉大学,保藏编号为CCTCCNO:M2014090。
具体实施方式
实施例1
将丝枝霉菌株(Aphanocladiumsp.)SK34.001在下述条件下进行发酵:
斜面培养:采用PDA培养基,各组分以g/L计:马铃薯200,葡萄糖20,琼脂20,自然pH,115℃灭菌30min。培养条件为:培养温度30℃,培养时间5天;
种子培养:采用牛肉膏蛋白胨培养基,各组分以g/L计:牛肉膏2.5,胰蛋白胨5.0,氯化钠2.5,自然pH,121℃灭菌20min。培养条件为:250mL三角瓶装液30mL,摇瓶转速200rpm,培养温度30℃,培养时间24h;
发酵培养:发酵培养基组分以g/L计:麸皮35,硫酸铵4.0,磷酸二氢钾2.0,硫酸镁0.3,氯化钙0.3,自然pH,121℃灭菌20min。培养条件为:种子培养液按体积百分数2%接种量接种于发酵培养基中,摇瓶转速150rpm,培养温度30℃,培养时间7天,得到发酵液的酶活为5U/mL。
实施例2
β-葡萄糖苷酶酶粉制备:
将实施例1制得的发酵液在8000rpm的转速下离心30min去除菌体即得发酵上清液,经超滤除去盐和杂蛋白,再经硫酸铵沉淀、透析,最后将透析液进行冷冻干燥即得β-葡萄糖苷酶酶粉。
<210>SEQIDNO:1
<211>596
<212>DNA
<213>丝枝霉(Aphanocladiumsp.)SK34.001
<400>1
tccgtaggtgaacctgcggagggatcattacagagtttacaactcccaaaccctcatgtg60
aacataccacgatgttgcttcggcggactcgccccggcgtccggacggcctagcgccgcc120
cgcggcccggatccaggcggccgccggagaccaccaaaactattttgtatcagcagtttt180
ttctgaatccgccgcaaggcaaaacaaatgaatcaaaactttcaacaacggatctcttgg240
ttctggcatcgatgaagaacgcagcgaaatgcgataagtaatgtgaattgcagaattcag300
tgaatcatcgaatctttgaacgcacattgcgcccgccagcattctggcgggcatgcctgt360
tcgagcgtcatttcaaccctcgacttccctttggggaaatcggcgttggggactggcagc420
ataccgccggccccgaaatggagtggcggcccgtccgcggcgacctctgcgtagtaatcc480
aacctcgcaccggaaccccgacgtggccacgccgtaaaacaccccactttctgaacgttg540
acctcggatcaggtaggaatacccgctgaacttaagcatatcaataagcggaggaa596
Claims (2)
1.一株丝枝霉菌株,其分类命名为丝枝霉(Aphanocladiumsp.)SK34.001,其保藏号为CCTCCNO:M2014090,保藏单位为中国典型培养物保藏中心。
2.权利要求1所述丝枝霉菌株CCTCCNO:M2014090生产β-葡萄糖苷酶的方法,其特征在于步骤如下:
(1)斜面培养:取丝枝霉菌株CCTCCNO:M2014090进行斜面培养,采用PDA培养基,各组分以g/L计:马铃薯200,葡萄糖20,琼脂15~20;自然pH,115℃下灭菌30min;培养温度为25~35℃,培养时间3~8天;
(2)种子培养:采用牛肉膏蛋白胨培养基,各组分以g/L计:牛肉膏2~5,胰蛋白胨5~8,氯化钠2~5,自然pH,121℃灭菌20min;250mL三角瓶装液30~50mL,将步骤(1)所得的斜面种子接种于种子培养基进行种子培养,摇瓶转速150~200rpm,培养温度25~35℃,培养时间18~24h;
(3)发酵培养:发酵培养基组分以g/L计:麸皮20~40,硫酸铵4~6,磷酸二氢钾2~3,硫酸镁0.3~0.5,氯化钙0.3~0.5,自然pH,121℃灭菌20min;步骤(2)所得的种子培养液按体积百分数2%~5%接种量接种于发酵培养基中,摇瓶转速150~200rpm,培养温度25~35℃,培养时间3~8天;
(4)β-葡萄糖苷酶酶粉制备:将步骤(3)制得的发酵液在5000~10000rpm离心10~30min或过滤去除菌体即得发酵上清液,经超滤除去盐和杂蛋白,再经硫酸铵沉淀、透析,最后将透析液进行冷冻干燥即得β-葡萄糖苷酶酶粉。
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CN1248287A (zh) * | 1997-02-26 | 2000-03-22 | 诺沃挪第克公司 | 微生物木糖葡聚糖内切转糖基酶(xet) |
CN1282377A (zh) * | 1997-10-17 | 2001-01-31 | Dsm有限公司 | 用于制备β-内酰胺抗生素的方法 |
WO2002014540A1 (en) * | 2000-08-11 | 2002-02-21 | Cornell Research Foundation, Inc. | Production and use of inducible enzymes from trichoderma and bacteria for control of plant pests and for industrial processes |
AU2001294362A1 (en) * | 2000-09-08 | 2002-03-22 | Dsm N.V. | An enzymatic process for preparing beta-lactam compounds |
EP1556500A1 (en) * | 2002-10-31 | 2005-07-27 | Bioferma Murcia, S.A. | Simple enzymatic process for preparing cefazolin |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1248287A (zh) * | 1997-02-26 | 2000-03-22 | 诺沃挪第克公司 | 微生物木糖葡聚糖内切转糖基酶(xet) |
CN1282377A (zh) * | 1997-10-17 | 2001-01-31 | Dsm有限公司 | 用于制备β-内酰胺抗生素的方法 |
WO2002014540A1 (en) * | 2000-08-11 | 2002-02-21 | Cornell Research Foundation, Inc. | Production and use of inducible enzymes from trichoderma and bacteria for control of plant pests and for industrial processes |
AU2001294362A1 (en) * | 2000-09-08 | 2002-03-22 | Dsm N.V. | An enzymatic process for preparing beta-lactam compounds |
EP1556500A1 (en) * | 2002-10-31 | 2005-07-27 | Bioferma Murcia, S.A. | Simple enzymatic process for preparing cefazolin |
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