CN113754785B - 融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用 - Google Patents

融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用 Download PDF

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CN113754785B
CN113754785B CN202111161744.8A CN202111161744A CN113754785B CN 113754785 B CN113754785 B CN 113754785B CN 202111161744 A CN202111161744 A CN 202111161744A CN 113754785 B CN113754785 B CN 113754785B
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CN113754785A (zh
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汪家琦
周洪波
潘丽娜
朱玉玲
刘雯娴
王玉光
陈祝
戴智勇
程海娜
颜卫彬
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Ausnutria Dairy China Co ltd
Changsha Yun Kang Bio Technology Co ltd
Central South University
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Changsha Yun Kang Bio Technology Co ltd
Central South University
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Abstract

本发明涉及生物技术领域,尤其涉及融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用。本发明提供的融合蛋白可以显著增强α‑1,2‑岩藻糖基转移酶异源表达,在较短时间就可以实现细胞内该酶的大量累积,从而达到更高的酶活力和底物转换效率。

Description

融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用
技术领域
本发明涉及生物技术领域,尤其涉及融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用。
背景技术
α-1,2-岩藻糖基转移酶(EC 2.4.1.69.)能催化经核苷酸活化的岩藻糖基转移至末端是半乳糖基的受体上,形成α-1,2-糖苷键。岩藻糖基转移酶催化得到的岩藻糖基化产物包括寡糖、糖脂、糖蛋白等,具有广泛的健康益处;由于岩藻糖基化产物如岩藻糖基化寡糖能够参与细胞识别,肿瘤发现和病原体粘附、提供大脑发育和认知所需的潜在必需营养。因此,其在医药、食品、化妆品等工业中也具有广阔的应用前景。
已发现岩藻糖基转移酶的基因供体的微生物主要包括幽门螺杆菌、大肠杆菌、脆弱拟杆菌等,但是,这些野生菌株被认为是可致病微生物,不适合用于食品医药工业;并且其岩藻糖基转移酶产量均十分低下,缺乏直接开发的价值。
因此,本领域寄希望于通过基因工程手段异源表达获得α-1,2-岩藻糖基转移酶。但是,从目前的研究成果来看,在大肠杆菌等商业化菌株中异源表达岩藻糖基转移酶基因不仅初始表达量极低,还易形成包涵体;且岩藻糖基转移酶为胞内分泌,提取岩藻糖基转移酶需破壁,会导致酶活及酶量的损失;同时,以随机突变的方式改造岩藻糖基转移酶的底物结合结构域和催化结构域以提高酶活具有随机突变的不确定,会导致的筛选困难。上述技术均并不能够真正运用于工业生产,极大地阻碍了其产物的大规模应用。
因此,急需找到一种新的可克服表达量低、易形成包涵体等缺陷且可大幅度提高岩藻糖基转移酶表达量的方法。
发明内容
有鉴于此,本发明要解决的技术问题在于提供一种表达量高,且可溶性蛋白更高的融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用。
本发明提供的融合蛋白包括:融合短肽和α-1,2-岩藻糖基转移酶片段;
所述α-1,2-岩藻糖基转移酶片段的氨基酸序列如SEQ ID NO:1所示;
所述融合短肽的氨基酸序列如SEQ ID NO:2~5任一项所示。
本发明中,所述融合短肽位于α-1,2-岩藻糖基转移酶片段的N端。
一些实施例中,所述融合蛋白的氨基酸序列如SEQ ID NO:6~9所示。
本发明还提供了编码所述融合蛋白的核酸。
本发明中,编码所述融合蛋白的核酸序列的5’端还包括RBS序列。
一些实施例中,编码所述融合蛋白的核酸的序列如SEQ ID NO:10~13所示。
本发明还提供了一种表达载体,其含有所述核酸的表达载体。
本发明中,所述表达载体的骨架载体选自pET系列载体。一些具体实施例中,所述表达载体的骨架载体为pET22b。
本发明还提供了转化或转染有所述表达载体的宿主细胞。
一些实施例中,所述宿主细胞为大肠杆菌。一些具体实施例中,所述宿主细胞为大肠杆菌基因工程菌E.coli BL21(DE3)。
所述宿主细胞的构建方法包括:将构建获得的表达载体转化入宿主细胞。所述转化的方法为热激转化。
本发明所述融合蛋白的制备方法,其包括培养所述的宿主细胞,诱导融合蛋白的表达。
本发明所述突变体、核酸、表达载体、宿主细胞或所述制备方法制得的产物,在岩藻糖基化产物合成中的应用。
本发明还提供了一种促进岩藻糖基化产物的合成的生物制剂,其包括:所述的突变体,核酸,表达载体,宿主细胞或所述制备方法制得的产物。
一些实施例中,所述生物制剂的制备原料包含所述突变体的发酵液。
本发明还提供了岩藻糖基化产物的合成方法,其以乳糖为底物,以本发明所述生物制剂促进岩藻糖基化产物的合成。一些实施例中,所述合成的反应条件包括:在pH=6.0~8.0,20~40℃条件下反应10~120min。
本发明提供的融合蛋白,将α-1,2-岩藻糖基转移酶片段与RBS、3×FLAG、SUMO、HA或cMyc中的至少一种进行融合。所获得的融合蛋白表达量大,在较短时间就可以实现细胞内该酶的大量累积,并且具有更高的酶活力和底物转换效率。
附图说明
图1示SDS-PAGE检测蛋白表达量;
图2示HPLC检测产物种类和含量。
具体实施方式
本发明提供了融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用,本领域技术人员可以借鉴本文内容,适当改进工艺参数实现。特别需要指出的是,所有类似的替换和改动对本领域技术人员来说是显而易见的,它们都被视为包括在本发明。本发明的方法及应用已经通过较佳实施例进行了描述,相关人员明显能在不脱离本发明内容、精神和范围内对本文的方法和应用进行改动或适当变更与组合,来实现和应用本发明技术。
本发明中,所述融合短肽为亲水性较强的序列,通过将α-1,2-岩藻糖基转移酶(futC)与该融合短肽融合,提高融合蛋白的可溶性表达,减少包涵体的形成。本发明中,所述融合短肽包括3×FLAG、SUMO、HA或cMyc中的至少一种。一些实施例中,所述融合片段为3×FLAG(SEQ ID NO:2)、SUMO(SEQ ID NO:3)、HA(SEQ ID NO:4)或cMyc(SEQ ID NO:5)。
为了增强蛋白的表达,在编码融合蛋白的核酸序列的5’端添加RBS序列。
一些具体实施例中,所述融合蛋白为RBS-futC(SEQ ID NO:1)、RBS-3×FLAG-futC(SEQ ID NO:6)、RBS-SUMO-futC(SEQ ID NO:7)、RBS-HA-futC(SEQ ID NO:8)、RBS-cMyc-futC(SEQ ID NO:9)。
具体的,本发明中涉及的片段名称及序列如下:
futC的氨基酸序列为(SEQ ID NO:1):
MDMMAFKVVQICGGLGNQMFQYAFAKSLQKHLNTPVLLDITSFDWSNRKMQLELFPIDLPYASAKEIAIAKMQHLPKLVRDTLKCMGFDRVSQEIVFEYEPGLLKPSRLTYFYGYFQDPRYFDAISPLIKQTFTLPPPENGNNKKKEEEYHRKLALILAAKNSVFVHVRRGDYVGIGCQLGIDYQKKALEYIAKRVPNMELFVFCEDLKFTQNLDLGYPFMDMTTRDKEEEAYWDMLLMQSCKHGIIANSTYSWWAAYLINNPEKIIIGPKHWLFGHENILCKEWVKIESHFEVKSKKYNALE
编码futC的核酸序列为:
atggatatgatggcgttcaaggtggttcagatttgcggtggcctgggtaaccagatgttccaatatgcgtttgcgaaaagcctgcaaaagcacctgaacaccccggttctgctggacattaccagcttcgattggagcaaccgtaaaatgcagctggagctgtttccgatcgacctgccgtacgcgagcgcgaaagaaattgcgatcgcgaagatgcagcacctgccgaaactggtgcgtgacaccctgaagtgcatgggtttcgatcgtgttagccaagagatcgtgtttgagtatgaaccgggtctgctgaaaccgagccgtctgacctacttctatggctactttcaggacccgcgttacttcgatgcgattagcccgctgatcaagcaaacctttaccctgccgccgccggaaaacggcaacaacaagaagaaggaagaggagtatcaccgtaagctggcgctgattctggcggcgaaaaacagcgtgtttgttcacgtgcgtcgtggtgactacgttggtattggctgccagctgggcatcgattatcagaagaaggcgctggagtacatcgcgaagcgtgttccgaacatggagctgttcgtgttttgcgaagacctgaaattcacccagaacctggatctgggttatccgtttatggacatgaccacccgtgataaggaagaggaagcgtactgggatatgctgctgatgcaaagctgcaaacacggcatcattgcgaacagcacctattcctggtgggcggcgtacctgatcaacaacccggaaaagatcattatcggtccgaaacactggctgttcggccacgagaacattctgtgcaaagaatgggttaagatcgagagccactttgaagtgaaaagcaaaaagtacaacgcgctcgag
3×FLAG的氨基酸序列为(SEQ ID NO:2):
DYKDDDDKDYKDDDDKDYKDDDDK
编码3×FLAG的核酸序列为:
gattacaaggatgacgacgataaggattacaaggatgacgacgataaggattacaaggatgacgacgataag
SUMO的氨基酸序列为(SEQ ID NO:3):
LVPELNEKDDDQVQKALASRENTQLMNRDNIEITVRDFKTLAPRRWLNDTIIEFFMKYIEKSTPNTVAFNSFFYTNLSERGYQGVRRWMKRKKTQIDKLDKIFTPINLNQSHWALGIIDLKKKTIGYVDSLSNGPNAMSFAILTDLQKYVMEESKHTIGEDFDLIHLDCPQQPNGYDCGIYVCMNTLYGSADAPLDFDYKDAIRMRRFIAHLILTDALKSS
编码SUMO的核酸序列为:
ctggtgccggaactgaatgagaaagacgacgaccaggtgcagaaagccctggccagccgtgaaaacacccagctgatgaaccgcgacaacatcgagatcaccgtgcgtgacttcaagaccttagccccgcgccgctggctgaacgataccattatcgaattttttatgaaatatattgaaaaaagcaccccgaacaccgtggcatttaacagtttcttttataccaacctgagcgagcgcggttatcagggcgtgcgccgctggatgaaacgtaagaaaactcagattgataaactggataaaatcttcaccccgatcaacctgaatcagagccattgggccctgggcattattgatctgaagaagaaaactattggctatgttgatagcctgagcaacggcccgaacgccatgagcttcgccatcctgaccgatctgcagaagtatgtgatggaggagagcaagcacaccatcggcgaggatttcgacctgatccatctggattgcccgcagcagccgaacggctacgattgcggcatttatgtgtgcatgaacaccctgtatggcagcgccgatgcaccgctggatttcgactacaaggacgccattcgcatgcgccgctttattgcccacctgatcctgacagatgccctgaaaagcagc
HA的氨基酸序列为:YPYDVPDYA(SEQ ID NO:4)
编码HA的核酸序列为:tacccatacgacgtcccagactacgctc
cMyc的氨基酸序列为:EQKLISEEDL(SEQ ID NO:5)
编码cMyc的核酸序列为:gagcagaaactcatctctgaagaggatctgc
3×FLAG前RBS核酸序列为:agcgcgcggcaacctcgcgcgaacaatagagaaagaagattaaggaggtttttt
SUMO前RBS核酸序列为aacaattacaataaaacaacgtaaggaggttgatt
HA前RBS核酸序列为attctaaggaaatttgaagattaaggaggtttttt
cMyc前RBS核酸序列为gacggacaagtcagcttgtattataggtaaggaggtttatt
futC前RBS核酸序列为tttgtttaactttaagaaggagatata
RBS-3×FLAG-futC融合蛋白的氨基酸序列为(SEQ ID NO:6):
DYKDDDDKDYKDDDDKDYKDDDDKMDMMAFKVVQICGGLGNQMFQYAFAKSLQKHLNTPVLLDITSFDWSNRKMQLELFPIDLPYASAKEIAIAKMQHLPKLVRDTLKCMGFDRVSQEIVFEYEPGLLKPSRLTYFYGYFQDPRYFDAISPLIKQTFTLPPPENGNNKKKEEEYHRKLALILAAKNSVFVHVRRGDYVGIGCQLGIDYQKKALEYIAKRVPNMELFVFCEDLKFTQNLDLGYPFMDMTTRDKEEEAYWDMLLMQSCKHGIIANSTYSWWAAYLINNPEKIIIGPKHWLFGHENILCKEWVKIESHFEVKSKKYNALE
编码RBS-3×FLAG-futC融合蛋白的核酸序列为(SEQ ID NO:10):
agcgcgcggcaacctcgcgcgaacaatagagaaagaagattaaggaggttttttatggattacaaggatgacgacgataaggattacaaggatgacgacgataaggattacaaggatgacgacgataagatggatatgatggcgttcaaggtggttcagatttgcggtggcctgggtaaccagatgttccaatatgcgtttgcgaaaagcctgcaaaagcacctgaacaccccggttctgctggacattaccagcttcgattggagcaaccgtaaaatgcagctggagctgtttccgatcgacctgccgtacgcgagcgcgaaagaaattgcgatcgcgaagatgcagcacctgccgaaactggtgcgtgacaccctgaagtgcatgggtttcgatcgtgttagccaagagatcgtgtttgagtatgaaccgggtctgctgaaaccgagccgtctgacctacttctatggctactttcaggacccgcgttacttcgatgcgattagcccgctgatcaagcaaacctttaccctgccgccgccggaaaacggcaacaacaagaagaaggaagaggagtatcaccgtaagctggcgctgattctggcggcgaaaaacagcgtgtttgttcacgtgcgtcgtggtgactacgttggtattggctgccagctgggcatcgattatcagaagaaggcgctggagtacatcgcgaagcgtgttccgaacatggagctgttcgtgttttgcgaagacctgaaattcacccagaacctggatctgggttatccgtttatggacatgaccacccgtgataaggaagaggaagcgtactgggatatgctgctgatgcaaagctgcaaacacggcatcattgcgaacagcacctattcctggtgggcggcgtacctgatcaacaacccggaaaagatcattatcggtccgaaacactggctgttcggccacgagaacattctgtgcaaagaatgggttaagatcgagagccactttgaagtgaaaagcaaaaagtacaacgcgctcgag
RBS-SUMO-futC融合蛋白的氨基酸序列为(SEQ ID NO:7):
LVPELNEKDDDQVQKALASRENTQLMNRDNIEITVRDFKTLAPRRWLNDTIIEFFMKYIEKSTPNTVAFNSFFYTNLSERGYQGVRRWMKRKKTQIDKLDKIFTPINLNQSHWALGIIDLKKKTIGYVDSLSNGPNAMSFAILTDLQKYVMEESKHTIGEDFDLIHLDCPQQPNGYDCGIYVCMNTLYGSADAPLDFDYKDAIRMRRFIAHLILTDALKSSHMDMMAFKVVQICGGLGNQMFQYAFAKSLQKHLNTPVLLDITSFDWSNRKMQLELFPIDLPYASAKEIAIAKMQHLPKLVRDTLKCMGFDRVSQEIVFEYEPGLLKPSRLTYFYGYFQDPRYFDAISPLIKQTFTLPPPENGNNKKKEEEYHRKLALILAAKNSVFVHVRRGDYVGIGCQLGIDYQKKALEYIAKRVPNMELFVFCEDLKFTQNLDLGYPFMDMTTRDKEEEAYWDMLLMQSCKHGIIANSTYSWWAAYLINNPEKIIIGPKHWLFGHENILCKEWVKIESHFEVKSKKYNALE
编码RBS-SUMO-futC融合蛋白的核酸序列为(SEQ ID NO:11):
aacaattacaataaaacaacgtaaggaggttgattatgctggtgccggaactgaatgagaaagacgacgaccaggtgcagaaagccctggccagccgtgaaaacacccagctgatgaaccgcgacaacatcgagatcaccgtgcgtgacttcaagaccttagccccgcgccgctggctgaacgataccattatcgaattttttatgaaatatattgaaaaaagcaccccgaacaccgtggcatttaacagtttcttttataccaacctgagcgagcgcggttatcagggcgtgcgccgctggatgaaacgtaagaaaactcagattgataaactggataaaatcttcaccccgatcaacctgaatcagagccattgggccctgggcattattgatctgaagaagaaaactattggctatgttgatagcctgagcaacggcccgaacgccatgagcttcgccatcctgaccgatctgcagaagtatgtgatggaggagagcaagcacaccatcggcgaggatttcgacctgatccatctggattgcccgcagcagccgaacggctacgattgcggcatttatgtgtgcatgaacaccctgtatggcagcgccgatgcaccgctggatttcgactacaaggacgccattcgcatgcgccgctttattgcccacctgatcctgacagatgccctgaaaagcagccatatggatatgatggcgttcaaggtggttcagatttgcggtggcctgggtaaccagatgttccaatatgcgtttgcgaaaagcctgcaaaagcacctgaacaccccggttctgctggacattaccagcttcgattggagcaaccgtaaaatgcagctggagctgtttccgatcgacctgccgtacgcgagcgcgaaagaaattgcgatcgcgaagatgcagcacctgccgaaactggtgcgtgacaccctgaagtgcatgggtttcgatcgtgttagccaagagatcgtgtttgagtatgaaccgggtctgctgaaaccgagccgtctgacctacttctatggctactttcaggacccgcgttacttcgatgcgattagcccgctgatcaagcaaacctttaccctgccgccgccggaaaacggcaacaacaagaagaaggaagaggagtatcaccgtaagctggcgctgattctggcggcgaaaaacagcgtgtttgttcacgtgcgtcgtggtgactacgttggtattggctgccagctgggcatcgattatcagaagaaggcgctggagtacatcgcgaagcgtgttccgaacatggagctgttcgtgttttgcgaagacctgaaattcacccagaacctggatctgggttatccgtttatggacatgaccacccgtgataaggaagaggaagcgtactgggatatgctgctgatgcaaagctgcaaacacggcatcattgcgaacagcacctattcctggtgggcggcgtacctgatcaacaacccggaaaagatcattatcggtccgaaacactggctgttcggccacgagaacattctgtgcaaagaatgggttaagatcgagagccactttgaagtgaaaagcaaaaagtacaacgcgctcgag
RBS-HA-futC融合蛋白的氨基酸序列为(SEQ ID NO:8):
YPYDVPDYAHMDMMAFKVVQICGGLGNQMFQYAFAKSLQKHLNTPVLLDITSFDWSNRKMQLELFPIDLPYASAKEIAIAKMQHLPKLVRDTLKCMGFDRVSQEIVFEYEPGLLKPSRLTYFYGYFQDPRYFDAISPLIKQTFTLPPPENGNNKKKEEEYHRKLALILAAKNSVFVHVRRGDYVGIGCQLGIDYQKKALEYIAKRVPNMELFVFCEDLKFTQNLDLGYPFMDMTTRDKEEEAYWDMLLMQSCKHGIIANSTYSWWAAYLINNPEKIIIGPKHWLFGHENILCKEWVKIESHFEVKSKKYNALE
编码RBS-HA-futC融合蛋白核酸序列为(SEQ ID NO:12):
attctaaggaaatttgaagattaaggaggttttttatgtacccatacgacgtcccagactacgctcatatggatatgatggcgttcaaggtggttcagatttgcggtggcctgggtaaccagatgttccaatatgcgtttgcgaaaagcctgcaaaagcacctgaacaccccggttctgctggacattaccagcttcgattggagcaaccgtaaaatgcagctggagctgtttccgatcgacctgccgtacgcgagcgcgaaagaaattgcgatcgcgaagatgcagcacctgccgaaactggtgcgtgacaccctgaagtgcatgggtttcgatcgtgttagccaagagatcgtgtttgagtatgaaccgggtctgctgaaaccgagccgtctgacctacttctatggctactttcaggacccgcgttacttcgatgcgattagcccgctgatcaagcaaacctttaccctgccgccgccggaaaacggcaacaacaagaagaaggaagaggagtatcaccgtaagctggcgctgattctggcggcgaaaaacagcgtgtttgttcacgtgcgtcgtggtgactacgttggtattggctgccagctgggcatcgattatcagaagaaggcgctggagtacatcgcgaagcgtgttccgaacatggagctgttcgtgttttgcgaagacctgaaattcacccagaacctggatctgggttatccgtttatggacatgaccacccgtgataaggaagaggaagcgtactgggatatgctgctgatgcaaagctgcaaacacggcatcattgcgaacagcacctattcctggtgggcggcgtacctgatcaacaacccggaaaagatcattatcggtccgaaacactggctgttcggccacgagaacattctgtgcaaagaatgggttaagatcgagagccactttgaagtgaaaagcaaaaagtacaacgcgctcgag
RBS-cMyc-futC融合蛋白的氨基酸序列为(SEQ ID NO:9):
EQKLISEEDLHMDMMAFKVVQICGGLGNQMFQYAFAKSLQKHLNTPVLLDITSFDWSNRKMQLELFPIDLPYASAKEIAIAKMQHLPKLVRDTLKCMGFDRVSQEIVFEYEPGLLKPSRLTYFYGYFQDPRYFDAISPLIKQTFTLPPPENGNNKKKEEEYHRKLALILAAKNSVFVHVRRGDYVGIGCQLGIDYQKKALEYIAKRVPNMELFVFCEDLKFTQNLDLGYPFMDMTTRDKEEEAYWDMLLMQSCKHGIIANSTYSWWAAYLINNPEKIIIGPKHWLFGHENILCKEWVKIESHFEVKSKKYNALE
编码RBS-cMyc-futC融合蛋白的核酸序列为(SEQ ID NO:13):
gacggacaagtcagcttgtattataggtaaggaggtttattatggagcagaaactcatctctgaagaggatctgcatatggatatgatggcgttcaaggtggttcagatttgcggtggcctgggtaaccagatgttccaatatgcgtttgcgaaaagcctgcaaaagcacctgaacaccccggttctgctggacattaccagcttcgattggagcaaccgtaaaatgcagctggagctgtttccgatcgacctgccgtacgcgagcgcgaaagaaattgcgatcgcgaagatgcagcacctgccgaaactggtgcgtgacaccctgaagtgcatgggtttcgatcgtgttagccaagagatcgtgtttgagtatgaaccgggtctgctgaaaccgagccgtctgacctacttctatggctactttcaggacccgcgttacttcgatgcgattagcccgctgatcaagcaaacctttaccctgccgccgccggaaaacggcaacaacaagaagaaggaagaggagtatcaccgtaagctggcgctgattctggcggcgaaaaacagcgtgtttgttcacgtgcgtcgtggtgactacgttggtattggctgccagctgggcatcgattatcagaagaaggcgctggagtacatcgcgaagcgtgttccgaacatggagctgttcgtgttttgcgaagacctgaaattcacccagaacctggatctgggttatccgtttatggacatgaccacccgtgataaggaagaggaagcgtactgggatatgctgctgatgcaaagctgcaaacacggcatcattgcgaacagcacctattcctggtgggcggcgtacctgatcaacaacccggaaaagatcattatcggtccgaaacactggctgttcggccacgagaacattctgtgcaaagaatgggttaagatcgagagccactttgaagtgaaaagcaaaaagtacaacgcgctcgag
本发明提供的表达载体中,编码所述融合蛋白的核酸插入在骨架载体中。本发明对构建重组载体的方法没有特殊限制,采用本领域常规方法即可。本发明实施中,所述骨架载体为pET系列载体。具体实施例中,采用的骨架在题为pET22b。
本发明所述转化或转染有表达载体的宿主细胞,优选的以大肠杆菌作为宿主菌;所述大肠杆菌优选的包括E.coli BL21(DE3),NovaBlue,Origami,PlySs,T7 shuffle等DE3系列菌株。本发明对所述重组菌的构建方法没有特殊限制,采用本领域常规方法即可。本发明具体实施过程中,所述重组菌采用以下方法制备得到:所述将表达载体转化E.coliBL21,获得重组菌。
本发明中所述融合蛋白优选的采用以下方法制备得到:培养所述重组菌,诱导获得融合蛋白。所述培养的方法包括活化和发酵。活化步骤中,采用的培养基为LB培养基。发酵步骤中培养基为TB培养基。所述培养温度优选为37℃,所述培养的时间以培养物的OD600达到0.6-0.8为准,所述诱导的方式优选为在培养基中加入终浓度为0.1~1.0mM的异丙基-β-D-硫代吡喃半乳糖苷(IPTG),于16~37℃诱导培养4~28h。
取上述诱导后的发酵液经离心取菌体破碎后取上清液,用于促进岩藻糖基化产物的合成。本发明的具体实施过程中,以GDP-L-岩藻糖和乳糖、乙酰基乳糖等为底物,所述的α-1,2-岩藻糖基转移酶突变体或其重组菌,无辅酶,在20-40℃,与pH值为6.0-8.0的缓冲液构成的体外催化反应体系中反应0.1-2h,得到包括α-1,2-岩藻糖基转移酶突变体的混合酶促反应体系。
一些实施例中,所述岩藻糖基化产物为2’-岩藻糖基乳糖。一些具体实施例中,所述2’-岩藻糖基乳糖的制备方法包括:将发酵菌体裂解后的上清液加入含有GDP-岩藻糖和乳糖的TRIS-HCl缓冲发酵液中,于20-40℃下孵育10-120min,获得含有2’-岩藻糖基乳糖的反应液。
本发明采用的试材皆为普通市售品,皆可于市场购得。下面结合实施例,进一步阐述本发明:
实施例1
(1)异源表达幽门螺杆菌来源的α-1,2-岩藻糖基转移酶
全基因合成NCBI上公布的幽门螺旋杆菌(Helicobacter pylori J166)的α-1,2-岩藻糖基转移酶基因futC序列,通过PCR对futC基因和表达载体pET22b进行扩增,使用DpnI酶消化模板质粒,随后将其转化到大肠杆菌DH5α感受态细胞,过夜培养后转化至大肠杆菌BL21感受态细胞,37℃复苏1h涂布于终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h。最后挑选氨苄霉素抗性平板上的单菌落进行菌落PCR验证,并通过测序确认α-1,2-岩藻糖基转移酶FutC是否构建成功,测序正确的质粒为pET22b-futC。
(2)构建协同优化融合蛋白质粒pET22b-RBS-3×FLAG-futC
合成所需RBS序列、RBS序列-3×FLAG片段和融合于蛋白质N端的外源序列;
以上述步骤(1)中测序正确的重组质粒pET22b-futC为模板,设置合适酶切位点进行酶切,纯化回收pET22b-futC线性化载体片段。然后使用T4连接酶将RBS片段、3×FLAG片段和线性化载体pET22b-futC进行重组连接。其中,RBS序连接到futC基因的N端,构建协同优化融合蛋白序列RBS-futC。RBS和3×FLAG的基因序列按顺序连接到futC基因的N端,构建协同优化融合蛋白序列RBS-3×FLAG-futC。
重组反应体系转化到大肠杆菌DH5α感受态细胞,过夜培养后转化至大肠杆菌BL21感受态细胞,37℃复苏1h涂布终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h。最后挑选氨苄霉素抗性平板上的单菌落进行菌落PCR验证,并通过测序确认融合蛋白RBS-futC(SEQ ID NO:1)、RBS-3×FLAG-futC(SEQ ID NO:6)是否构建成功。
实施例2:
构建协同优化融合蛋白载体pET22b-RBS-SUMO-futC
全基因合成RBS-sumo的基因片段,随后制备pET22b-futC线性化载体片段,步骤同实施例1。然后使用T4连接酶将sumo基因片段和线性化载体pET22b-futC进行重组连接。其中,RBS-sumo的基因序列连接到futC基因的N端,构建协同优化融合蛋白RBS-SUMO-futC。重组反应体系转化到大肠杆菌DH5α感受态细胞,过夜培养后转化至大肠杆菌BL21感受态细胞,37℃复苏1h涂布终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h。最后挑选氨苄霉素抗性平板上的单菌落进行菌落PCR验证,并通过测序确认融合蛋白RBS-SUMO-futC(SEQ ID NO:7)是否构建成功。
实施例3:
构建协同优化融合蛋白载体pET22b-RBS-HA-futC
全基因合成RBS-HA的基因片段,随后制备pET22b-futC线性化载体片段,步骤同实施例1。然后使用T4连接酶将RBS-HA基因和线性化载体pET22b-futC进行重组连接。其中,RBS-HA的基因序列连接到futC基因的N端,构建协同优化融合蛋白RBS-HA-futC。重组反应体系转化到大肠杆菌DH5α感受态细胞,过夜培养后转化至大肠杆菌BL21感受态细胞,37℃复苏1h涂布终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h。最后挑选氨苄霉素抗性平板上的单菌落进行菌落PCR验证,并通过测序确认融合蛋白RBS-HA-futC(SEQ ID NO:8)是否构建成功。
实施例4:
构建协同优化融合蛋白载体pET22b-RBS-cMyc-futC
全基因合成RBS-cMyc的基因序列,随后制备pET22b-futC线性化载体片段,步骤同实施例1。然后使用T4连接酶将RBS-cMyc基因和线性化载体pET22b-futC进行重组连接。其中,RBS-cMyc的基因序列连接到futC基因的N端,构建协同优化融合蛋白RBS-cMyc-futC。重组反应体系转化到大肠杆菌DH5α感受态细胞,过夜培养后转化至大肠杆菌BL21感受态细胞,37℃复苏1h涂布终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h。最后挑选氨苄霉素抗性平板上的单菌落进行菌落PCR验证,并通过测序确认融合蛋白RBS-cMyc-futC(SEQ ID NO:9)是否构建成功。
实施例5:
摇瓶发酵重验证重组菌产酶能力
将上述实施例和对比例测序正确的重组质粒pET22b-futC、、pET22b-RBS-futC、pET22b-RBS-3×FLAG-futC、pET22b-RBS-SUMO-futC、pET22b-RBS-HA-futC和pET22b-RBS-cMyc-futC分别转入BL21感受态中,37℃复苏1h涂布终浓度为0.1mM的氨苄霉素抗性LB平板,37℃培养10-16h,以获得不同含有RBS和N端融合蛋白的的pET22b-RBS-FP-futC发酵重组菌。挑取单菌落到终浓度为0.1mM氨苄霉素的LB培养基(胰蛋白胨10g/L、酵母粉5g/L、NaCl10g/L)中培养8-10h,作为摇瓶发酵的种子液。然后将种子液按1%的接种量接入到装有20-25mL发酵培养基的250mL三角瓶中,同时添加终浓度为0.1mM的氨苄霉素,发酵培养基的配方是:1.2%(W/V)胰蛋白胨,2.4%(W/V)酵母提取物,0.4%(V/V)甘油,磷酸盐缓冲液17mM KH2PO4,72mM K2HPO4。随后将三角瓶置于37℃、200r/min条件下培养2-4h后,添加终浓度为0.25mM的IPTG至摇瓶中,于26℃、150r/min条件下培养2-10h。
首先取20mL发酵液在12000rpm下离心15-20min后,收集菌体,重悬后经超声波破碎,低温高速离心得到细胞破碎上清液。利用组氨酸标签亲和纯化原理,使用Ni-NTA对目标蛋白进行纯化。细胞破碎上清液穿流镍柱三次,后用洗涤液洗(Tris-HCl缓冲体系,10mM咪唑浓度)去除非亲和吸附的杂蛋白,最后用洗脱液(Tris-HCl缓冲体系,500mM咪唑浓度)洗脱目标蛋白,洗脱三次,分别收集。通过透析除去洗脱液中的咪唑,最终得到较纯的重组融合蛋白。
将上清液加入含有GDP-岩藻糖和乳糖的TRIS-HCl缓冲发酵液中,于20-40℃下孵育10-120min。反应结束后,将反应液通过除盐柱进行超滤除杂后,再通过0.22μm的滤膜,备用。对各成分进行SDS-PAGE电泳检测,结果如图1。其中,M:marker FT:穿流液Sup:细胞破碎上清液E2:第二遍洗脱液。CK为未进行RBS和N端协同优化的FUTC蛋白,Ropt为只进行RBS区域优化的融合蛋白,Fhf RBS和HA序列协同优化的融合蛋白、Fmcf RBS和cMYC序列协同优化的融合蛋白、F3Ff RBS和3×FLAG序列协同优化的融合蛋白、Fsf RBS和SUMO序列协同优化的融合蛋白。采用bradford法统计各融合蛋白的表达量,结果如表1。
酶活检测:
首先取20mL发酵液在12000rpm下离心15-20min后,收集菌体,重悬后经超声波破碎,低温高速离心得到细胞破碎上清液。经组氨酸标签纯化得到较纯的酶液,并通过透析除去咪唑、调整缓冲液盐浓度。最终得到的酶液保存备用。
加入100μM GDP-L-岩藻糖100μL和5mM乳糖100μL,而后加入250μL酶液,在20-40℃下孵育10-120min,实现催化生成2'-FL。催化完成后立即置于冰上停止反应。随后在低温下高速离心并通过除盐柱进行超滤除杂后,采用高效液相色谱仪(HPLC)测定催化体系中的2'-FL产量以及底物的剩余量。
将催化得到的反应液,通过0.22μm的滤膜,备用。准备液相色谱检测所需的流动相,流动相A:乙腈,流动相B=0.5%醋酸三乙胺的水溶液。选用amide色谱柱(150mm×2.1um),检测条件为:流动相比例80:20,流速0.2m/L,柱温35℃,检测器使用蒸发光散射检测器,蒸发温度70℃,载气流量为2.0SLM。通过外标法定量产物。HPLC检测结果如图2所示。
在催化体系的样品中,产生了新的物质峰,检测到了产物2'-FL生成,并且观察到GDP-岩藻糖物质峰的减少和消失。通过外标法,利用峰面积计算物质的含量,此时产物产量为4.01μM 2'-FL/mM Lactose。
表1
表达量(g/L) 酶活力(U/mL)
futC 0.09 0.41
RBS-futC 0.46 2.34
RBS-3×FLAG-futC 1.15 6.03
RBS-SUMO-futC 0.84 3.44
RBS-HA-futC 0.70 1.22
RBS-cMyc-futC 0.84 2.14
结果显示:
本发明通过先设计不同强度的RBS序列替换载体上原有部分,然后将亲水性不同的外源序列融合至岩藻糖基转移酶基因N端,并在表达宿主中进行表达,成功将岩藻糖基转移酶的表达量提高至野生型菌株发酵的将近12倍;
将本发明的重组大肠杆菌重组菌诱导培养5h,可使得胞内的岩藻糖基转移酶酶活提高13.71倍;
本发明实现了岩藻糖基转移酶在工程化大肠杆菌中的高效表达,且提高了酶活力,在工业生产中具有巨大的应用前景。
以上仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
序列表
<110> 中南大学;澳优乳业(中国)有限公司;长沙运康生物科技有限公司
<120> 融合蛋白及其制备方法与在制备岩藻糖基化产物中的应用
<130> MP21018069
<160> 13
<170> SIPOSequenceListing 1.0
<210> 1
<211> 303
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 1
Met Asp Met Met Ala Phe Lys Val Val Gln Ile Cys Gly Gly Leu Gly
1 5 10 15
Asn Gln Met Phe Gln Tyr Ala Phe Ala Lys Ser Leu Gln Lys His Leu
20 25 30
Asn Thr Pro Val Leu Leu Asp Ile Thr Ser Phe Asp Trp Ser Asn Arg
35 40 45
Lys Met Gln Leu Glu Leu Phe Pro Ile Asp Leu Pro Tyr Ala Ser Ala
50 55 60
Lys Glu Ile Ala Ile Ala Lys Met Gln His Leu Pro Lys Leu Val Arg
65 70 75 80
Asp Thr Leu Lys Cys Met Gly Phe Asp Arg Val Ser Gln Glu Ile Val
85 90 95
Phe Glu Tyr Glu Pro Gly Leu Leu Lys Pro Ser Arg Leu Thr Tyr Phe
100 105 110
Tyr Gly Tyr Phe Gln Asp Pro Arg Tyr Phe Asp Ala Ile Ser Pro Leu
115 120 125
Ile Lys Gln Thr Phe Thr Leu Pro Pro Pro Glu Asn Gly Asn Asn Lys
130 135 140
Lys Lys Glu Glu Glu Tyr His Arg Lys Leu Ala Leu Ile Leu Ala Ala
145 150 155 160
Lys Asn Ser Val Phe Val His Val Arg Arg Gly Asp Tyr Val Gly Ile
165 170 175
Gly Cys Gln Leu Gly Ile Asp Tyr Gln Lys Lys Ala Leu Glu Tyr Ile
180 185 190
Ala Lys Arg Val Pro Asn Met Glu Leu Phe Val Phe Cys Glu Asp Leu
195 200 205
Lys Phe Thr Gln Asn Leu Asp Leu Gly Tyr Pro Phe Met Asp Met Thr
210 215 220
Thr Arg Asp Lys Glu Glu Glu Ala Tyr Trp Asp Met Leu Leu Met Gln
225 230 235 240
Ser Cys Lys His Gly Ile Ile Ala Asn Ser Thr Tyr Ser Trp Trp Ala
245 250 255
Ala Tyr Leu Ile Asn Asn Pro Glu Lys Ile Ile Ile Gly Pro Lys His
260 265 270
Trp Leu Phe Gly His Glu Asn Ile Leu Cys Lys Glu Trp Val Lys Ile
275 280 285
Glu Ser His Phe Glu Val Lys Ser Lys Lys Tyr Asn Ala Leu Glu
290 295 300
<210> 2
<211> 24
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 2
Asp Tyr Lys Asp Asp Asp Asp Lys Asp Tyr Lys Asp Asp Asp Asp Lys
1 5 10 15
Asp Tyr Lys Asp Asp Asp Asp Lys
20
<210> 3
<211> 221
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 3
Leu Val Pro Glu Leu Asn Glu Lys Asp Asp Asp Gln Val Gln Lys Ala
1 5 10 15
Leu Ala Ser Arg Glu Asn Thr Gln Leu Met Asn Arg Asp Asn Ile Glu
20 25 30
Ile Thr Val Arg Asp Phe Lys Thr Leu Ala Pro Arg Arg Trp Leu Asn
35 40 45
Asp Thr Ile Ile Glu Phe Phe Met Lys Tyr Ile Glu Lys Ser Thr Pro
50 55 60
Asn Thr Val Ala Phe Asn Ser Phe Phe Tyr Thr Asn Leu Ser Glu Arg
65 70 75 80
Gly Tyr Gln Gly Val Arg Arg Trp Met Lys Arg Lys Lys Thr Gln Ile
85 90 95
Asp Lys Leu Asp Lys Ile Phe Thr Pro Ile Asn Leu Asn Gln Ser His
100 105 110
Trp Ala Leu Gly Ile Ile Asp Leu Lys Lys Lys Thr Ile Gly Tyr Val
115 120 125
Asp Ser Leu Ser Asn Gly Pro Asn Ala Met Ser Phe Ala Ile Leu Thr
130 135 140
Asp Leu Gln Lys Tyr Val Met Glu Glu Ser Lys His Thr Ile Gly Glu
145 150 155 160
Asp Phe Asp Leu Ile His Leu Asp Cys Pro Gln Gln Pro Asn Gly Tyr
165 170 175
Asp Cys Gly Ile Tyr Val Cys Met Asn Thr Leu Tyr Gly Ser Ala Asp
180 185 190
Ala Pro Leu Asp Phe Asp Tyr Lys Asp Ala Ile Arg Met Arg Arg Phe
195 200 205
Ile Ala His Leu Ile Leu Thr Asp Ala Leu Lys Ser Ser
210 215 220
<210> 4
<211> 9
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 4
Tyr Pro Tyr Asp Val Pro Asp Tyr Ala
1 5
<210> 5
<211> 10
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 5
Glu Gln Lys Leu Ile Ser Glu Glu Asp Leu
1 5 10
<210> 6
<211> 327
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 6
Asp Tyr Lys Asp Asp Asp Asp Lys Asp Tyr Lys Asp Asp Asp Asp Lys
1 5 10 15
Asp Tyr Lys Asp Asp Asp Asp Lys Met Asp Met Met Ala Phe Lys Val
20 25 30
Val Gln Ile Cys Gly Gly Leu Gly Asn Gln Met Phe Gln Tyr Ala Phe
35 40 45
Ala Lys Ser Leu Gln Lys His Leu Asn Thr Pro Val Leu Leu Asp Ile
50 55 60
Thr Ser Phe Asp Trp Ser Asn Arg Lys Met Gln Leu Glu Leu Phe Pro
65 70 75 80
Ile Asp Leu Pro Tyr Ala Ser Ala Lys Glu Ile Ala Ile Ala Lys Met
85 90 95
Gln His Leu Pro Lys Leu Val Arg Asp Thr Leu Lys Cys Met Gly Phe
100 105 110
Asp Arg Val Ser Gln Glu Ile Val Phe Glu Tyr Glu Pro Gly Leu Leu
115 120 125
Lys Pro Ser Arg Leu Thr Tyr Phe Tyr Gly Tyr Phe Gln Asp Pro Arg
130 135 140
Tyr Phe Asp Ala Ile Ser Pro Leu Ile Lys Gln Thr Phe Thr Leu Pro
145 150 155 160
Pro Pro Glu Asn Gly Asn Asn Lys Lys Lys Glu Glu Glu Tyr His Arg
165 170 175
Lys Leu Ala Leu Ile Leu Ala Ala Lys Asn Ser Val Phe Val His Val
180 185 190
Arg Arg Gly Asp Tyr Val Gly Ile Gly Cys Gln Leu Gly Ile Asp Tyr
195 200 205
Gln Lys Lys Ala Leu Glu Tyr Ile Ala Lys Arg Val Pro Asn Met Glu
210 215 220
Leu Phe Val Phe Cys Glu Asp Leu Lys Phe Thr Gln Asn Leu Asp Leu
225 230 235 240
Gly Tyr Pro Phe Met Asp Met Thr Thr Arg Asp Lys Glu Glu Glu Ala
245 250 255
Tyr Trp Asp Met Leu Leu Met Gln Ser Cys Lys His Gly Ile Ile Ala
260 265 270
Asn Ser Thr Tyr Ser Trp Trp Ala Ala Tyr Leu Ile Asn Asn Pro Glu
275 280 285
Lys Ile Ile Ile Gly Pro Lys His Trp Leu Phe Gly His Glu Asn Ile
290 295 300
Leu Cys Lys Glu Trp Val Lys Ile Glu Ser His Phe Glu Val Lys Ser
305 310 315 320
Lys Lys Tyr Asn Ala Leu Glu
325
<210> 7
<211> 525
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 7
Leu Val Pro Glu Leu Asn Glu Lys Asp Asp Asp Gln Val Gln Lys Ala
1 5 10 15
Leu Ala Ser Arg Glu Asn Thr Gln Leu Met Asn Arg Asp Asn Ile Glu
20 25 30
Ile Thr Val Arg Asp Phe Lys Thr Leu Ala Pro Arg Arg Trp Leu Asn
35 40 45
Asp Thr Ile Ile Glu Phe Phe Met Lys Tyr Ile Glu Lys Ser Thr Pro
50 55 60
Asn Thr Val Ala Phe Asn Ser Phe Phe Tyr Thr Asn Leu Ser Glu Arg
65 70 75 80
Gly Tyr Gln Gly Val Arg Arg Trp Met Lys Arg Lys Lys Thr Gln Ile
85 90 95
Asp Lys Leu Asp Lys Ile Phe Thr Pro Ile Asn Leu Asn Gln Ser His
100 105 110
Trp Ala Leu Gly Ile Ile Asp Leu Lys Lys Lys Thr Ile Gly Tyr Val
115 120 125
Asp Ser Leu Ser Asn Gly Pro Asn Ala Met Ser Phe Ala Ile Leu Thr
130 135 140
Asp Leu Gln Lys Tyr Val Met Glu Glu Ser Lys His Thr Ile Gly Glu
145 150 155 160
Asp Phe Asp Leu Ile His Leu Asp Cys Pro Gln Gln Pro Asn Gly Tyr
165 170 175
Asp Cys Gly Ile Tyr Val Cys Met Asn Thr Leu Tyr Gly Ser Ala Asp
180 185 190
Ala Pro Leu Asp Phe Asp Tyr Lys Asp Ala Ile Arg Met Arg Arg Phe
195 200 205
Ile Ala His Leu Ile Leu Thr Asp Ala Leu Lys Ser Ser His Met Asp
210 215 220
Met Met Ala Phe Lys Val Val Gln Ile Cys Gly Gly Leu Gly Asn Gln
225 230 235 240
Met Phe Gln Tyr Ala Phe Ala Lys Ser Leu Gln Lys His Leu Asn Thr
245 250 255
Pro Val Leu Leu Asp Ile Thr Ser Phe Asp Trp Ser Asn Arg Lys Met
260 265 270
Gln Leu Glu Leu Phe Pro Ile Asp Leu Pro Tyr Ala Ser Ala Lys Glu
275 280 285
Ile Ala Ile Ala Lys Met Gln His Leu Pro Lys Leu Val Arg Asp Thr
290 295 300
Leu Lys Cys Met Gly Phe Asp Arg Val Ser Gln Glu Ile Val Phe Glu
305 310 315 320
Tyr Glu Pro Gly Leu Leu Lys Pro Ser Arg Leu Thr Tyr Phe Tyr Gly
325 330 335
Tyr Phe Gln Asp Pro Arg Tyr Phe Asp Ala Ile Ser Pro Leu Ile Lys
340 345 350
Gln Thr Phe Thr Leu Pro Pro Pro Glu Asn Gly Asn Asn Lys Lys Lys
355 360 365
Glu Glu Glu Tyr His Arg Lys Leu Ala Leu Ile Leu Ala Ala Lys Asn
370 375 380
Ser Val Phe Val His Val Arg Arg Gly Asp Tyr Val Gly Ile Gly Cys
385 390 395 400
Gln Leu Gly Ile Asp Tyr Gln Lys Lys Ala Leu Glu Tyr Ile Ala Lys
405 410 415
Arg Val Pro Asn Met Glu Leu Phe Val Phe Cys Glu Asp Leu Lys Phe
420 425 430
Thr Gln Asn Leu Asp Leu Gly Tyr Pro Phe Met Asp Met Thr Thr Arg
435 440 445
Asp Lys Glu Glu Glu Ala Tyr Trp Asp Met Leu Leu Met Gln Ser Cys
450 455 460
Lys His Gly Ile Ile Ala Asn Ser Thr Tyr Ser Trp Trp Ala Ala Tyr
465 470 475 480
Leu Ile Asn Asn Pro Glu Lys Ile Ile Ile Gly Pro Lys His Trp Leu
485 490 495
Phe Gly His Glu Asn Ile Leu Cys Lys Glu Trp Val Lys Ile Glu Ser
500 505 510
His Phe Glu Val Lys Ser Lys Lys Tyr Asn Ala Leu Glu
515 520 525
<210> 8
<211> 313
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 8
Tyr Pro Tyr Asp Val Pro Asp Tyr Ala His Met Asp Met Met Ala Phe
1 5 10 15
Lys Val Val Gln Ile Cys Gly Gly Leu Gly Asn Gln Met Phe Gln Tyr
20 25 30
Ala Phe Ala Lys Ser Leu Gln Lys His Leu Asn Thr Pro Val Leu Leu
35 40 45
Asp Ile Thr Ser Phe Asp Trp Ser Asn Arg Lys Met Gln Leu Glu Leu
50 55 60
Phe Pro Ile Asp Leu Pro Tyr Ala Ser Ala Lys Glu Ile Ala Ile Ala
65 70 75 80
Lys Met Gln His Leu Pro Lys Leu Val Arg Asp Thr Leu Lys Cys Met
85 90 95
Gly Phe Asp Arg Val Ser Gln Glu Ile Val Phe Glu Tyr Glu Pro Gly
100 105 110
Leu Leu Lys Pro Ser Arg Leu Thr Tyr Phe Tyr Gly Tyr Phe Gln Asp
115 120 125
Pro Arg Tyr Phe Asp Ala Ile Ser Pro Leu Ile Lys Gln Thr Phe Thr
130 135 140
Leu Pro Pro Pro Glu Asn Gly Asn Asn Lys Lys Lys Glu Glu Glu Tyr
145 150 155 160
His Arg Lys Leu Ala Leu Ile Leu Ala Ala Lys Asn Ser Val Phe Val
165 170 175
His Val Arg Arg Gly Asp Tyr Val Gly Ile Gly Cys Gln Leu Gly Ile
180 185 190
Asp Tyr Gln Lys Lys Ala Leu Glu Tyr Ile Ala Lys Arg Val Pro Asn
195 200 205
Met Glu Leu Phe Val Phe Cys Glu Asp Leu Lys Phe Thr Gln Asn Leu
210 215 220
Asp Leu Gly Tyr Pro Phe Met Asp Met Thr Thr Arg Asp Lys Glu Glu
225 230 235 240
Glu Ala Tyr Trp Asp Met Leu Leu Met Gln Ser Cys Lys His Gly Ile
245 250 255
Ile Ala Asn Ser Thr Tyr Ser Trp Trp Ala Ala Tyr Leu Ile Asn Asn
260 265 270
Pro Glu Lys Ile Ile Ile Gly Pro Lys His Trp Leu Phe Gly His Glu
275 280 285
Asn Ile Leu Cys Lys Glu Trp Val Lys Ile Glu Ser His Phe Glu Val
290 295 300
Lys Ser Lys Lys Tyr Asn Ala Leu Glu
305 310
<210> 9
<211> 314
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 9
Glu Gln Lys Leu Ile Ser Glu Glu Asp Leu His Met Asp Met Met Ala
1 5 10 15
Phe Lys Val Val Gln Ile Cys Gly Gly Leu Gly Asn Gln Met Phe Gln
20 25 30
Tyr Ala Phe Ala Lys Ser Leu Gln Lys His Leu Asn Thr Pro Val Leu
35 40 45
Leu Asp Ile Thr Ser Phe Asp Trp Ser Asn Arg Lys Met Gln Leu Glu
50 55 60
Leu Phe Pro Ile Asp Leu Pro Tyr Ala Ser Ala Lys Glu Ile Ala Ile
65 70 75 80
Ala Lys Met Gln His Leu Pro Lys Leu Val Arg Asp Thr Leu Lys Cys
85 90 95
Met Gly Phe Asp Arg Val Ser Gln Glu Ile Val Phe Glu Tyr Glu Pro
100 105 110
Gly Leu Leu Lys Pro Ser Arg Leu Thr Tyr Phe Tyr Gly Tyr Phe Gln
115 120 125
Asp Pro Arg Tyr Phe Asp Ala Ile Ser Pro Leu Ile Lys Gln Thr Phe
130 135 140
Thr Leu Pro Pro Pro Glu Asn Gly Asn Asn Lys Lys Lys Glu Glu Glu
145 150 155 160
Tyr His Arg Lys Leu Ala Leu Ile Leu Ala Ala Lys Asn Ser Val Phe
165 170 175
Val His Val Arg Arg Gly Asp Tyr Val Gly Ile Gly Cys Gln Leu Gly
180 185 190
Ile Asp Tyr Gln Lys Lys Ala Leu Glu Tyr Ile Ala Lys Arg Val Pro
195 200 205
Asn Met Glu Leu Phe Val Phe Cys Glu Asp Leu Lys Phe Thr Gln Asn
210 215 220
Leu Asp Leu Gly Tyr Pro Phe Met Asp Met Thr Thr Arg Asp Lys Glu
225 230 235 240
Glu Glu Ala Tyr Trp Asp Met Leu Leu Met Gln Ser Cys Lys His Gly
245 250 255
Ile Ile Ala Asn Ser Thr Tyr Ser Trp Trp Ala Ala Tyr Leu Ile Asn
260 265 270
Asn Pro Glu Lys Ile Ile Ile Gly Pro Lys His Trp Leu Phe Gly His
275 280 285
Glu Asn Ile Leu Cys Lys Glu Trp Val Lys Ile Glu Ser His Phe Glu
290 295 300
Val Lys Ser Lys Lys Tyr Asn Ala Leu Glu
305 310
<210> 10
<211> 1038
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 10
agcgcgcggc aacctcgcgc gaacaataga gaaagaagat taaggaggtt ttttatggat 60
tacaaggatg acgacgataa ggattacaag gatgacgacg ataaggatta caaggatgac 120
gacgataaga tggatatgat ggcgttcaag gtggttcaga tttgcggtgg cctgggtaac 180
cagatgttcc aatatgcgtt tgcgaaaagc ctgcaaaagc acctgaacac cccggttctg 240
ctggacatta ccagcttcga ttggagcaac cgtaaaatgc agctggagct gtttccgatc 300
gacctgccgt acgcgagcgc gaaagaaatt gcgatcgcga agatgcagca cctgccgaaa 360
ctggtgcgtg acaccctgaa gtgcatgggt ttcgatcgtg ttagccaaga gatcgtgttt 420
gagtatgaac cgggtctgct gaaaccgagc cgtctgacct acttctatgg ctactttcag 480
gacccgcgtt acttcgatgc gattagcccg ctgatcaagc aaacctttac cctgccgccg 540
ccggaaaacg gcaacaacaa gaagaaggaa gaggagtatc accgtaagct ggcgctgatt 600
ctggcggcga aaaacagcgt gtttgttcac gtgcgtcgtg gtgactacgt tggtattggc 660
tgccagctgg gcatcgatta tcagaagaag gcgctggagt acatcgcgaa gcgtgttccg 720
aacatggagc tgttcgtgtt ttgcgaagac ctgaaattca cccagaacct ggatctgggt 780
tatccgttta tggacatgac cacccgtgat aaggaagagg aagcgtactg ggatatgctg 840
ctgatgcaaa gctgcaaaca cggcatcatt gcgaacagca cctattcctg gtgggcggcg 900
tacctgatca acaacccgga aaagatcatt atcggtccga aacactggct gttcggccac 960
gagaacattc tgtgcaaaga atgggttaag atcgagagcc actttgaagt gaaaagcaaa 1020
aagtacaacg cgctcgag 1038
<210> 11
<211> 1613
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 11
aacaattaca ataaaacaac gtaaggaggt tgattatgct ggtgccggaa ctgaatgaga 60
aagacgacga ccaggtgcag aaagccctgg ccagccgtga aaacacccag ctgatgaacc 120
gcgacaacat cgagatcacc gtgcgtgact tcaagacctt agccccgcgc cgctggctga 180
acgataccat tatcgaattt tttatgaaat atattgaaaa aagcaccccg aacaccgtgg 240
catttaacag tttcttttat accaacctga gcgagcgcgg ttatcagggc gtgcgccgct 300
ggatgaaacg taagaaaact cagattgata aactggataa aatcttcacc ccgatcaacc 360
tgaatcagag ccattgggcc ctgggcatta ttgatctgaa gaagaaaact attggctatg 420
ttgatagcct gagcaacggc ccgaacgcca tgagcttcgc catcctgacc gatctgcaga 480
agtatgtgat ggaggagagc aagcacacca tcggcgagga tttcgacctg atccatctgg 540
attgcccgca gcagccgaac ggctacgatt gcggcattta tgtgtgcatg aacaccctgt 600
atggcagcgc cgatgcaccg ctggatttcg actacaagga cgccattcgc atgcgccgct 660
ttattgccca cctgatcctg acagatgccc tgaaaagcag ccatatggat atgatggcgt 720
tcaaggtggt tcagatttgc ggtggcctgg gtaaccagat gttccaatat gcgtttgcga 780
aaagcctgca aaagcacctg aacaccccgg ttctgctgga cattaccagc ttcgattgga 840
gcaaccgtaa aatgcagctg gagctgtttc cgatcgacct gccgtacgcg agcgcgaaag 900
aaattgcgat cgcgaagatg cagcacctgc cgaaactggt gcgtgacacc ctgaagtgca 960
tgggtttcga tcgtgttagc caagagatcg tgtttgagta tgaaccgggt ctgctgaaac 1020
cgagccgtct gacctacttc tatggctact ttcaggaccc gcgttacttc gatgcgatta 1080
gcccgctgat caagcaaacc tttaccctgc cgccgccgga aaacggcaac aacaagaaga 1140
aggaagagga gtatcaccgt aagctggcgc tgattctggc ggcgaaaaac agcgtgtttg 1200
ttcacgtgcg tcgtggtgac tacgttggta ttggctgcca gctgggcatc gattatcaga 1260
agaaggcgct ggagtacatc gcgaagcgtg ttccgaacat ggagctgttc gtgttttgcg 1320
aagacctgaa attcacccag aacctggatc tgggttatcc gtttatggac atgaccaccc 1380
gtgataagga agaggaagcg tactgggata tgctgctgat gcaaagctgc aaacacggca 1440
tcattgcgaa cagcacctat tcctggtggg cggcgtacct gatcaacaac ccggaaaaga 1500
tcattatcgg tccgaaacac tggctgttcg gccacgagaa cattctgtgc aaagaatggg 1560
ttaagatcga gagccacttt gaagtgaaaa gcaaaaagta caacgcgctc gag 1613
<210> 12
<211> 977
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 12
attctaagga aatttgaaga ttaaggaggt tttttatgta cccatacgac gtcccagact 60
acgctcatat ggatatgatg gcgttcaagg tggttcagat ttgcggtggc ctgggtaacc 120
agatgttcca atatgcgttt gcgaaaagcc tgcaaaagca cctgaacacc ccggttctgc 180
tggacattac cagcttcgat tggagcaacc gtaaaatgca gctggagctg tttccgatcg 240
acctgccgta cgcgagcgcg aaagaaattg cgatcgcgaa gatgcagcac ctgccgaaac 300
tggtgcgtga caccctgaag tgcatgggtt tcgatcgtgt tagccaagag atcgtgtttg 360
agtatgaacc gggtctgctg aaaccgagcc gtctgaccta cttctatggc tactttcagg 420
acccgcgtta cttcgatgcg attagcccgc tgatcaagca aacctttacc ctgccgccgc 480
cggaaaacgg caacaacaag aagaaggaag aggagtatca ccgtaagctg gcgctgattc 540
tggcggcgaa aaacagcgtg tttgttcacg tgcgtcgtgg tgactacgtt ggtattggct 600
gccagctggg catcgattat cagaagaagg cgctggagta catcgcgaag cgtgttccga 660
acatggagct gttcgtgttt tgcgaagacc tgaaattcac ccagaacctg gatctgggtt 720
atccgtttat ggacatgacc acccgtgata aggaagagga agcgtactgg gatatgctgc 780
tgatgcaaag ctgcaaacac ggcatcattg cgaacagcac ctattcctgg tgggcggcgt 840
acctgatcaa caacccggaa aagatcatta tcggtccgaa acactggctg ttcggccacg 900
agaacattct gtgcaaagaa tgggttaaga tcgagagcca ctttgaagtg aaaagcaaaa 960
agtacaacgc gctcgag 977
<210> 13
<211> 986
<212> DNA
<213> 人工序列(Artificial Sequence)
<400> 13
gacggacaag tcagcttgta ttataggtaa ggaggtttat tatggagcag aaactcatct 60
ctgaagagga tctgcatatg gatatgatgg cgttcaaggt ggttcagatt tgcggtggcc 120
tgggtaacca gatgttccaa tatgcgtttg cgaaaagcct gcaaaagcac ctgaacaccc 180
cggttctgct ggacattacc agcttcgatt ggagcaaccg taaaatgcag ctggagctgt 240
ttccgatcga cctgccgtac gcgagcgcga aagaaattgc gatcgcgaag atgcagcacc 300
tgccgaaact ggtgcgtgac accctgaagt gcatgggttt cgatcgtgtt agccaagaga 360
tcgtgtttga gtatgaaccg ggtctgctga aaccgagccg tctgacctac ttctatggct 420
actttcagga cccgcgttac ttcgatgcga ttagcccgct gatcaagcaa acctttaccc 480
tgccgccgcc ggaaaacggc aacaacaaga agaaggaaga ggagtatcac cgtaagctgg 540
cgctgattct ggcggcgaaa aacagcgtgt ttgttcacgt gcgtcgtggt gactacgttg 600
gtattggctg ccagctgggc atcgattatc agaagaaggc gctggagtac atcgcgaagc 660
gtgttccgaa catggagctg ttcgtgtttt gcgaagacct gaaattcacc cagaacctgg 720
atctgggtta tccgtttatg gacatgacca cccgtgataa ggaagaggaa gcgtactggg 780
atatgctgct gatgcaaagc tgcaaacacg gcatcattgc gaacagcacc tattcctggt 840
gggcggcgta cctgatcaac aacccggaaa agatcattat cggtccgaaa cactggctgt 900
tcggccacga gaacattctg tgcaaagaat gggttaagat cgagagccac tttgaagtga 960
aaagcaaaaa gtacaacgcg ctcgag 986

Claims (7)

1.核酸,其核苷酸序列如SEQ ID NO:10~13所示。
2.含有权利要求1所述核酸的表达载体。
3.宿主细胞,其转化或转染有权利要求2所述表达载体。
4.融合蛋白的制备方法,其特征在于,包括培养权利要求3所述的宿主细胞,诱导融合蛋白的表达。
5.权利要求1所述的核酸,权利要求2所述的表达载体或权利要求3所述的宿主细胞在岩藻糖基化产物合成中的应用,所述岩藻糖基化产物为2’-岩藻糖基乳糖。
6.一种促进岩藻糖基化产物的合成的生物制剂,其特征在于,包括:权利要求1所述的核酸,权利要求2所述的表达载体或权利要求3所述的宿主细胞。
7.岩藻糖基化产物的合成方法,其特征在于,以乳糖为底物,以权利要求6所述的生物制剂促进岩藻糖基化产物的合成;所述岩藻糖基化产物为2’-岩藻糖基乳糖。
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101724614A (zh) * 2010-01-12 2010-06-09 中南大学 一种酸性β-甘露聚糖酶、基因、工程菌及其构建
WO2013102492A1 (en) * 2012-01-04 2013-07-11 Instytut Biochemii I Biofizyki Pan Synthetic genes encoding peptide fragments of natural myelin proteins for induction of oral tolerance, dna fragment comprising these genes, means of obtaining these peptides in a microbial (bacterial) system and their medical application
WO2015199386A1 (ko) * 2014-06-23 2015-12-30 서울대학교산학협력단 가용성 단백질 발현량이 증대된 헬리코박터 파일로리 유래 α-1,2 푸코실 전달효소의 유전자와 단백질 및 α-1,2 푸코실올리고당 생산에의 응용
CN109554385A (zh) * 2018-07-24 2019-04-02 石家庄葛兰德生物科技有限公司 一种基因工程菌制备2-岩藻糖基乳糖的方法
WO2020072617A1 (en) * 2018-10-02 2020-04-09 Zimitech, Inc. Use of substrate importers for the export of oligosaccharides

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101724614A (zh) * 2010-01-12 2010-06-09 中南大学 一种酸性β-甘露聚糖酶、基因、工程菌及其构建
WO2013102492A1 (en) * 2012-01-04 2013-07-11 Instytut Biochemii I Biofizyki Pan Synthetic genes encoding peptide fragments of natural myelin proteins for induction of oral tolerance, dna fragment comprising these genes, means of obtaining these peptides in a microbial (bacterial) system and their medical application
WO2015199386A1 (ko) * 2014-06-23 2015-12-30 서울대학교산학협력단 가용성 단백질 발현량이 증대된 헬리코박터 파일로리 유래 α-1,2 푸코실 전달효소의 유전자와 단백질 및 α-1,2 푸코실올리고당 생산에의 응용
CN109554385A (zh) * 2018-07-24 2019-04-02 石家庄葛兰德生物科技有限公司 一种基因工程菌制备2-岩藻糖基乳糖的方法
WO2020072617A1 (en) * 2018-10-02 2020-04-09 Zimitech, Inc. Use of substrate importers for the export of oligosaccharides

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
alpha-(1,2) fucosyltransferase [Helicobacter pylori];GenBank;《GenBank》;GenBank: ABO61750.1 *
Direct RBS Engineering of the biosynthetic gene cluster for efficient productivity of violaceins in E. coli;Yuyang Zhang等;《Microbial Cell Factories》;第20卷;第1-13页 *
Enhancing heterologous expression of a key enzyme for the biosynthesis of 20-fucosyllactose;Wenxian Liu等;《J Sci Food Agric》;第102卷;第5162-5171页 *
利用RBS序列策略在大肠杆菌中高效合成异戊二烯;娄陈美等;《生物技术》;第30卷(第5期);第431-438页 *

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