CN111471605A - 一株高产岩藻糖基乳糖的酿酒酵母工程菌株及其应用 - Google Patents

一株高产岩藻糖基乳糖的酿酒酵母工程菌株及其应用 Download PDF

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CN111471605A
CN111471605A CN202010187309.1A CN202010187309A CN111471605A CN 111471605 A CN111471605 A CN 111471605A CN 202010187309 A CN202010187309 A CN 202010187309A CN 111471605 A CN111471605 A CN 111471605A
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孟祥锋
刘巍峰
徐明远
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Abstract

本发明公开了一种高产2’‑岩藻糖基乳糖的酿酒酵母工程菌株,通过代谢工程改造,使得酿酒酵母可以吸收乳糖并在胞内以GDP‑甘露糖为前体合成GDP‑岩藻糖,并通过异源表达来源于蜡样芽孢杆菌中的α‑1,2‑岩藻糖基转移酶,所得到的重组菌株可以高产2’‑岩藻糖基乳糖,为工业化生产2’‑岩藻糖基乳糖提供重要参考。

Description

一株高产岩藻糖基乳糖的酿酒酵母工程菌株及其应用
技术领域
本发明属于基因工程领域,尤其涉及一株高产岩藻糖基乳糖,尤其是高产2’-岩藻糖基乳糖的重组酿酒酵母及其应用。
背景技术
2’-岩藻糖基乳糖(2-FL)作为母乳寡糖中的重要组成部分,可以促进人体肠道内有益微生物如双歧杆菌等的生长,降低肠道内病原体感染的风险,还可以调控免疫应答。目前2-FL已在婴幼儿配方奶粉中作为添加剂使用。2-FL的大量合成具有良好的经济效益。化学合成2-FL过程中需添加有毒试剂,难以应用于食品工业。
在生物体内合成2-FL是行之有效的方法。2-FL的生物合成过程已较为清楚:一分子供体GDP-岩藻糖在α-1,2-岩藻糖基转移酶的作用下与受体乳糖结合,产生一分子2-FL。现有技术中有研究构建了高产2-FL的大肠杆菌重组菌株。但是大肠杆菌可能产生内毒素,影响产品的分离纯化难度及产品安全性;另外大肠杆菌发酵时易受到噬菌体的污染,这使大肠杆菌工业化生产2-FL受到了制约。
酿酒酵母是被普遍认为安全的微生物,已有研究利用酿酒酵母合成2-FL;但是,现有报道中酿酒酵母菌株合成的2-FL产量仅0.5g/L,难以满足工业化生产的需要。制约酿酒酵母中2-FL产量的重要因素之一为α-1,2-岩藻糖基转移酶的酶活性不足。寻找具有高活力的α-1,2-岩藻糖基转移酶可能会提高酿酒酵母中2-FL的产量。
发明内容
本发明通过代谢工程改造,使得酿酒酵母可以吸收乳糖并在胞内以GDP-甘露糖为前体合成GDP-岩藻糖,并通过异源表达来源于蜡样芽孢杆菌中的α-1,2-岩藻糖基转移酶,得到了高产2-FL的酿酒酵母工程菌株。
一方面,本发明提供了一株高产2’-岩藻糖基乳糖的酿酒酵母工程菌株,所述酿酒酵母工程菌株中含有重组的乳糖透性酶(Lactose permease)、重组的GDP-甘露糖脱水酶(GDP-mannose-4,6-dehydratase)、重组的GDP-岩藻糖合酶(GDP-L-fucose synthase)以及重组的α-1,2-岩藻糖基转移酶(α-1,2 fucosyltransferase)。
本发明中,术语“重组”指通过转化将目的基因转移到酿酒酵母中;所述含有重组的目的基因的酿酒酵母工程菌株与其来源的野生型酿酒酵母相比,其已经以遗传方式修饰,从而展示出改变的或不同的基因型和/或表型。可以通过将目的蛋白通过载体在宿主菌中进行表达(包括过表达的方式)来实现,还可以通过将目的蛋白的编码基因重组到宿主菌的基因组上来实现。
含有重组的目的基因的酿酒酵母工程菌株含有至少一个被引入的基因序列,此类基因序列包括但不限于天然存在或不存在酿酒酵母中的基因以及希望引入到酿酒酵母细胞中的其他基因或DNA序列,无论野生型的酿酒酵母中是否已经存在相同或类似的基因或DNA序列;在一些实施方式中,引入的基因序列将通过例如同源重组或定点诱变来修饰或甚至替代内源基因或DNA序列;在其他的实施方式中,引入到酿酒酵母工程菌株中的重组基因可以是与存在酿酒酵母中的DNA序列相同的并且被引入以提供DNA的一个或多个另外的拷贝,从而DNA的基因产物过表达或修饰的表达。
在优选的实施方式中,所述α-1,2-岩藻糖基转移酶来源于蜡样芽孢杆菌(Bacillus cereus),更优选的,所述α-1,2-岩藻糖基转移酶的氨基酸序列如SEQ ID No.11所示。
更优选的,所述酿酒酵母工程菌株包含重组的α-1,2-岩藻糖基转移酶的编码基因;优选的,所述编码基因的序列如SEQ ID No.12所示。
优选的,所述乳糖透性酶来源于乳酸克鲁维斯酵母,更优选的,所述乳糖透性酶的氨基酸序列如SEQ ID No.1所示。
优选的,所述GDP-甘露糖脱水酶和GDP-岩藻糖合酶来源于大肠杆菌,优选,来源于大肠杆菌K12,更优选的,所述GDP-甘露糖脱水酶的氨基酸序列如SEQ ID No.3所示,所述GDP-岩藻糖合酶的氨基酸序列如SEQ ID No.5所示。
在优选的实施方式中,所述酿酒酵母工程菌株的出发菌株为酿酒酵母W303-1a。
另一方面,本发明还提供了所述的酿酒酵母工程菌株的制备方法,所述方法包括将所述目的基因重组到酿酒酵母中的步骤。
优选的,将所述目的基因整合到酿酒酵母的基因组中。
进一步的,所述目的基因的整合位点包括TRP1、URA3或LEU2。
另一方面,本发明还提供了所述酿酒酵母工程菌株在生产2’-岩藻糖基乳糖中的应用。
本发明以酿酒酵母W303-1a为出发菌株。从克鲁维斯酵母总DNA中克隆出乳糖透性酶Lac12,构建表达盒Pgal1-lac12-Tcyc1,并通过无缝融合的方法将表达盒与pRS304连接。所得到的重组载体以限制性内切酶Bsu36I线性化后,通过醋酸锂转化法转入酿酒酵母W303-1a中,并通过色氨酸缺陷的YNB固体平板筛选得到阳性克隆。进一步PCR验证后,所得到的正确转化子命名为FL01。FL01可以吸收胞外添加的乳糖。从大肠杆菌K12总DNA中克隆出GDP-甘露糖脱水酶(Gmd)以及GDP-岩藻糖合成酶(WcaG),以来源于pUMRI-A的双向启动子gal1,10构建双向表达盒Pgal1-gmd-Tcyc1&Pgal10-wcaG-Tadh1。将以上表达盒通过无缝融合的方法与pRS306连接,所得到的重组载体以NcoI限制性内切酶线性化,随后通过醋酸锂转化法转入FL01中,验证正确的重组菌株命名为FL03,该菌株可以吸收胞外的乳糖,同时可以以胞内的GDP-甘露糖为底物,合成GDP-岩藻糖。
以包括Helicobactor pylori、Acetobacter sp.、Bacillus cereus、Bacteroidesunifomis、Bacteroides eggerthii、Neocallimastix californiae等菌株来源的α-1,2-岩藻糖基转移酶为基础,以PCR融合的方法构建表达盒,将表达盒连接在载体pRS305上,并通过醋酸锂转化法转入FL03中,其中,表达来源于Bacillus cereus的α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株可以产生约2.9g/L的2-FL。
现有技术中也有报道在酿酒酵母中合成2-FL,但是,所得到的酿酒酵母重组菌株中的2-FL产量仅为约0.5g/L。而本申请中利用来源于蜡样芽孢杆菌的α-1,2-岩藻糖基转移酶构建的酿酒酵母重组菌株,以半乳糖诱导相关基因的表达,发酵96h后2-FL产量可以达到2.9g/L,这为酿酒酵母工业化生产2-FL提供了重要的参考。
附图说明
图1.表达Lac12的酿酒酵母重组菌株可以将乳糖吸收至胞内;A,葡萄糖标准品;B,半乳糖标准品;C,乳糖标准品;D、E,表达Lac12的酿酒酵母重组菌株S-L胞内裂解液。
图2.异源表达Gmd和WcaG的酿酒酵母重组菌株FL03可以产生GDP-岩藻糖;A,GDP-岩藻糖标准品;B,表达Lac12的酿酒酵母重组菌株FL01;C,表达乳糖转运体Lac12和GDP-岩藻糖合成相关酶WcaG和Gmd的酿酒酵母重组菌株FL03。
图3.重组菌株FL04菌株可以产生2-FL;a,酿酒酵母重组菌株FL03;b的酿酒酵母重组菌株FL04。
图4.表达不同来源α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株中2-FL产量;FL04,表达来源于Helicobacter pylori中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株;FL05,表达来源于Acetobacter sp.中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株;FL06,表达来源于Bacillus cereus中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株;FL07,表达来源于Bacteroides eggerthii中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株;FL08,表达来源于Bacteroides unifomis中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株;FL09,表达来源于Neocallimastix californiae中α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株。以上菌株的出发菌株均为FL03。
实施方式
下面结合实施例对本发明做进一步的说明,以下所述,仅是对本发明的较佳实施例而已,并非对本发明做其他形式的限制,任何熟悉本专业的技术人员可能利用上述揭示的技术内容加以变更为同等变化的等效实施例。凡是未脱离本发明方案内容,依据本发明的技术实质对以下实施例所做的任何简单修改或等同变化,均落在本发明的保护范围内。
实施例一、可吸收乳糖的重组酿酒酵母基因工程菌株的构建
本实施例中的重组工程菌株的构建,以酿酒酵母W303-1a为出发菌株。
利用Omega试剂盒提取乳酸克鲁维斯酵母(Kluyveromyces lactis)的总DNA,使用引物Lac12-F和Lac12-R从其中扩增出乳糖透性酶(Lactose permease)的序列,命名为Lac12,其氨基酸序列如SEQ ID No.1所示,核酸序列如SEQ ID No.2所示。
以酿酒酵母(Saccharomyces cerevisiae)W303-1a总DNA为模板,以BamHI-GAL1-F和GAL1-LAC12-R为引物扩增出gal1启动子,以lac12-CYC1-F和CYC1-XhoI-R扩增出cyc1终止子,通过SOE-PCR构建Pgal1-lac12-Tcyc1表达盒,并通过无缝连接的方法连接在以BamHI和XhoI双酶切后的pRS304载体上,得到重组载体pRS304-Pgal1-lac12-Tcyc1。重组载体pRS304-Pgal1-lac12-Tcyc1以Bsu36I酶切,通过切胶纯化得到线性化片段。
以醋酸锂转化法,将线性化的pRS304-Pgal1-lac12-Tcyc1转入酿酒酵母W303-1a中,整合位点为TRP1。涂布于色氨酸缺陷的YNB固体平板上。转化子长出后挑取于色氨酸缺陷的YNB液体培养基中,提取总DNA进行PCR验证,正确的为阳性克隆子,命名为FL01。
上述引物序列如下表所示:
Figure BDA0002414647740000051
Figure BDA0002414647740000061
FL01菌株吸收乳糖能力验证:将FL01于添加2%半乳糖和0.2%乳糖的YP培养基中培养24h后,离心去上清,菌体冲洗两遍以后破碎,所得到的细胞裂解液进行TLC分析,TLC条件:薄层硅胶板购自Thermo公司,展开剂为水:冰醋酸:异丁醇=1:1:2,10h后,60℃下将硅胶板吹干,随后将硅胶板置于染色液(90%甲醇,10%浓硫酸,0.2%苔黑素)中浸润染色,260℃下吹干,显色。可以检测到胞内存在乳糖,如图1所示。
实施例二、产GDP-岩藻糖的重组酿酒酵母基因工程菌株的构建
从大肠杆菌(Escherichia coli)K12中,以引物GMD-F和GMD-R扩增出GDP-甘露糖脱水酶(GDP-mannose-4,6-dehydratase)的序列,命名为Gmd,其氨基酸序列如SEQ ID No.3所示,其核苷酸序列如SEQ ID No.4所示。以引物WcaG-F和WcaG-R扩增出GDP-岩藻糖合酶(GDP-L-fucose synthase)的序列,命名为WcaG,其氨基酸序列如SEQ ID No.5所示,其核苷酸序列如SEQ ID No.6所示。
以pUMRI-A质粒(Ye,L.,X.Lv,and H.Yu,Assembly of biosynthetic pathwaysin Saccharomyces cerevisiae using a marker recyclable integrative plasmidtoolbox.Frontiers of Chemical Engineering in China,2017.11(1):p.126-132.)为模板,wcag-10-F和10-gmd-R为引物扩增出双向启动子gal1,10。以酿酒酵母W303-1a总DNA为模板,以SacI-ADH1-F和ADH1-wcaG-R引物扩增出adh1终止子序列,以gmd-CYC1-F和CYC1-KpnI-R引物扩增出cyc1终止子序列。通过SOE-PCR的方法,将以上片段依次连接,得到双向基因表达盒Pgal1-gmd-Tcyc1&Pgal10-wcaG-Tadh1。并通过无缝连接的方法连在SacI和KpnI酶切后的载体pRS306上,得到重组载体pRS306-Pgal1-gmd-Tcyc1&Pgal10-wcaG-Tadh1。重组载体pRS306-Pgal1-gmd-Tcyc1&Pgal10-wcaG-Tadh1以NcoI酶线性化,切胶回收。
将线性化后的pRS306-Pgal1-gmd-Tcyc1&Pgal10-wcaG-Tadh1通过醋酸锂转化法转入实施例1得到的菌株FL01中,整合位点为URA3,涂布于色氨酸、尿嘧啶缺陷的YNB固体平板上。转化子长出后挑取于色氨酸、尿嘧啶缺陷的YNB液体培养基中,提取总DNA以引物SacI-ADH1-F和CYC1-KpnI-R进行PCR验证,正确的为阳性克隆子,命名为FL03。
所用引物如下表所示:
Figure BDA0002414647740000071
FL03菌株中GDP-岩藻糖的检测:将FL03于添加2%葡萄糖和2%半乳糖的YP培养基中培养48h后,离心去上清,菌体冲洗两遍以后破碎,所得到的细胞裂解液进行HPLC分析。所用HPLC仪器来自岛津公司,带有UV检测器,使用C18分析柱(Syncronis aQ 250*4.6*5μm,Thermo Fisher Scientific)进行分析,柱温25,℃流动相为20mM三乙胺,添加2%(v/v)乙腈,流速为0.6mL/min,样品进样量15μL,检测波长为254nm;可以检测到胞内存在GDP-岩藻糖,检测结果如图2所示,表明FL03菌株可以产生GDP-岩藻糖。
实施例三、产2’-岩藻糖基乳糖的重组酿酒酵母基因工程菌株的构建
以人类及幽门螺杆菌来源的α-1,2-岩藻糖基转移酶为模板,通过blast分析从Helicobacter pylori、Acetobacter sp.、Bacillus cereus、Bacteroides unifomis、Bacteroides eggerthii、Neocallimastix californiae菌株中发现新的α-1,2-岩藻糖基转移酶,分别命名为Futhp(氨基酸序列如SEQ ID No.7所示,核苷酸序列如SEQ ID No.8所示),Futas(氨基酸序列如SEQ ID No.9所示,核苷酸序列如SEQ ID No.10所示),Futbc(氨基酸序列如SEQ ID No.11所示,核苷酸序列如SEQ ID No.12所示),Futbu(氨基酸序列如SEQ ID No.15所示,核苷酸序列如SEQ ID No.16所示),Futbe(氨基酸序列如SEQ ID No.13所示,核苷酸序列如SEQ ID No.14所示),Futnc(氨基酸序列如SEQ ID No.17所示,核苷酸序列如SEQ ID No.18所示)。
将上述α-1,2-岩藻糖基转移酶编码序列以如下表所示引物扩增。以酿酒酵母W303-1a总DNA为模板分别扩增得到对应以上α-1,2-岩藻糖基转移酶的启动子gal1和终止子cyc1。通过SOE-PCR的方法融合对应片段,得到不同α-1,2-岩藻糖基转移酶的表达盒Pgal1-futC-Tcyc1。将表达盒分别与XbaI和HindIII酶切后的pRS305无缝连接,得到重组载体。所用引物如下表所示:
Figure BDA0002414647740000081
Figure BDA0002414647740000091
以上得到的重组载体均以BspTI酶切后,切胶回收。
将线性化后的上述构建的重组pRS305载体通过醋酸锂转化法转入实施例2得到的菌株FL03中,整合位点为LEU2,涂布于色氨酸、尿嘧啶、亮氨酸缺陷的YNB固体平板上。转化子长出后挑取于色氨酸、尿嘧啶、亮氨酸缺陷的YNB液体培养基中,提取总DNA进行PCR验证,正确的为阳性克隆子,将带有来源于Helicobacter pylori、Acetobacter sp.、Bacilluscereus、Bacteroides unifomis、Bacteroides eggerthii、Neocallimastix californiae菌株的α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株分别命名为FL04,FL05,FL06,FL07,FL08,FL09。
上述重组菌株中2-FL的检测方法:将菌株于添加2%葡萄糖、2%半乳糖和0.2%乳糖的YP培养基中培养96h后,离心取上清为胞外产物,菌体冲洗两遍以后破碎,所得到的细胞裂解液为胞内产物。将胞外及胞内产物进行HPLC分析。所用HPLC仪器来自岛津公司,带有RI检测器,使用Rezex ROA-Organic Acid H+(8%)column(Phenomenex,Torrance,CA,USA)分析柱进行分析,柱温50℃,流动相为0.005N的H2SO4,流速为0.6mL/min,样品进样量15μL,检测结果如图3所示,以重组菌株FL04为例,可在保留时间8min处检测到2-FL。进一步对表达不同来源α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株所产生的2-FL进行定量分析,结果如图4所示,其中,表达来源于Bacillus cereus(蜡样芽孢杆菌)的α-1,2-岩藻糖基转移酶的酿酒酵母重组菌株FL06中2-FL产量可达到约2.9g/L。上述实施例中所述菌株如下表所示:
Figure BDA0002414647740000101
上文中已经用一般性说明及具体实施方案对本发明作了详尽的描述,但在本发明基础上,可以对之作一些修改或改进,这对本领域技术人员而言是显而易见的。因此,在不偏离本发明精神的基础上所做的这些修改或改进,均属于本发明要求保护的范围。
SEQUENCE LISTING
<110> 山东大学
<120> 一株高产岩藻糖基乳糖的酿酒酵母工程菌株及其应用
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<170> PatentIn version 3.5
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Tyr Leu Ile Glu Asn Pro Glu Lys Ile Ile Ile Gly Pro Lys His Trp
260 265 270
Leu Phe Gly His Glu Asn Ile Leu Cys Lys Glu Trp Val Lys Ile Glu
275 280 285
Ser His Phe Glu Val Lys Ser Gln Lys Tyr Asn Ala
290 295 300
<210> 8
<211> 903
<212> DNA
<213> Helicobacter pylori
<400> 8
atggctttta aggtggtgca aatttgcgga gggcttggga atcaaatgtt tcaatacgct 60
ttcgctaaaa gtttgcaaaa acactctaat acgcctgtgc tgttagatat cacttctttt 120
gattggagcg ataggaaaat gcaattagaa cttttcccta ttgatttgcc ctatgcgagc 180
gcgaaagaaa tcgctatagc taaaatgcaa cacctcccca agctagtaag agacgcgctc 240
aaatgcatgg gatttgatag ggtgagtcaa gaaatcgttt ttgaatacga gcctaaattg 300
ctaaagccaa gccgcttgac ttattttttt ggctatttcc aagatccacg atactttgat 360
gctatatccc ctttaatcaa gcaaaccttc actctaccac caccaccaga aaataataag 420
aataataata aaaaagagga agaatatcag tgcaagcttt ctttgatttt agccgctaaa 480
aacagcgtgt ttgtgcatat aagaagaggg gattatgtgg ggattggctg tcagcttggt 540
attgactatc aaaaaaaggc gcttgagtat atggcaaagc gcgtgccaaa catggagctt 600
tttgtgtttt gcgaagactt agaattcacg caaaatcttg atcttggcta cccttttatg 660
gacatgacca ctagggataa agaagaagag gcgtattggg acatgctgct catgcaatct 720
tgtcagcatg gcattatcgc taatagcact tatagctggt gggcggccta tttgatagaa 780
aatccagaaa aaatcattat tggccccaaa cactggcttt ttgggcatga gaatatcctt 840
tgtaaggagt gggtgaaaat agaatcccat tttgaggtaa aatcccaaaa gtataacgct 900
taa 903
<210> 9
<211> 308
<212> PRT
<213> Acetobacter sp.
<400> 9
Met Ala Val Ser Pro Gln Glu Ser Lys Tyr Ser Ala His Val Ser Pro
1 5 10 15
Asp Lys Pro Leu Arg Ile Val Arg Leu Gly Gly Gly Leu Gly Asn Gln
20 25 30
Met Phe Gln Tyr Ala Phe Gly Leu Ala Ala Gly Asp Val Leu Trp Asp
35 40 45
Asn Thr Ser Phe Leu Thr Asn His Tyr Arg Ser Phe Asp Leu Gly Leu
50 55 60
Tyr Asn Ile Ser Gly Asp Phe Ala Ser Asn Glu Gln Ile Lys Lys Cys
65 70 75 80
Lys Asn Glu Ile Arg Phe Lys Asn Ile Leu Pro Arg Ser Ile Arg Lys
85 90 95
Lys Phe Asn Leu Gly Lys Phe Ile Tyr Leu Lys Thr Asn Arg Val Cys
100 105 110
Glu Arg Gln Ile Asn Arg Tyr Glu Pro Glu Leu Leu Ser Lys Asp Gly
115 120 125
Asp Val Tyr Tyr Asp Gly Val Phe Gln Thr Glu Lys Tyr Phe Lys Pro
130 135 140
Leu Arg Glu Arg Leu Leu His Asp Phe Thr Leu Thr Lys Pro Leu Asp
145 150 155 160
Ala Ala Asn Leu Asp Met Leu Ala Lys Ile Arg Ala Ala Asp Ala Val
165 170 175
Ala Val His Ile Arg Arg Gly Asp Tyr Leu Asn Pro Arg Ser Pro Phe
180 185 190
Thr Tyr Leu Asp Lys Asp Tyr Phe Leu Asn Ala Met Asp Tyr Ile Gly
195 200 205
Lys Arg Val Asp Lys Pro His Phe Phe Ile Phe Ser Ser Asp Thr Asp
210 215 220
Trp Val Arg Thr Asn Ile Gln Thr Ala Tyr Pro Gln Thr Ile Val Glu
225 230 235 240
Ile Asn Asp Glu Lys His Gly Tyr Phe Asp Leu Glu Leu Met Arg Asn
245 250 255
Cys Arg His Asn Ile Ile Ala Asn Ser Thr Phe Ser Trp Trp Gly Ala
260 265 270
Trp Leu Asn Thr Asn Pro Asp Lys Ile Val Val Ala Pro Lys Gln Trp
275 280 285
Phe Arg Pro Asp Ala Ala Glu Tyr Ser Gly Asp Ile Val Pro Asn Asp
290 295 300
Trp Ile Lys Leu
305
<210> 10
<211> 927
<212> DNA
<213> Acetobacter sp.
<400> 10
atggctgttt cacctcaaga aagcaaatat tccgcccatg tttccccgga taaaccgctg 60
cgtatcgtca ggctgggcgg agggctcggc aatcagatgt ttcaatatgc cttcggactg 120
gctgccggtg atgttttgtg ggacaatacc agctttttga ccaaccatta ccgcagtttt 180
gatttgggat tgtataacat cagcggagat tttgcctcaa atgaacaaat aaaaaaatgt 240
aaaaacgaaa tcagatttaa aaacattctt ccccgttcca tccgcaaaaa atttaatctg 300
ggaaaattta tttacctgaa aaccaaccgc gtctgcgaaa gacagattaa ccgttacgag 360
ccggaacttc taagcaaaga tggcgacgtt tattatgacg gagttttcca gaccgaaaaa 420
tattttaaac cgctgcgaga aaggctgttg catgatttta cgctgacaaa acctcttgat 480
gcagcgaatc ttgatatgct tgccaaaatc cgggctgccg atgccgttgc cgttcatatc 540
cgtcgcggcg actatcttaa tccgcgcagc ccttttactt atttggataa ggattatttt 600
ctgaatgcga tggattatat cgggaaacgc gttgataaac cgcatttctt tattttttcc 660
agtgatacag actgggttcg gactaatata caaacagcct atccgcagac tatcgttgaa 720
attaatgatg aaaaacacgg ctattttgac ttggaactga tgcggaactg ccgccataac 780
attatcgcca acagcacatt ttcgtggtgg ggagcctggc tgaatacaaa tccggacaag 840
attgtcgttg cgcctaagca atggttcagg ccggacgctg ccgaatattc cggtgatatc 900
gttcctaacg actggataaa gttataa 927
<210> 11
<211> 291
<212> PRT
<213> Bacillus cereus
<400> 11
Met Lys Ile Ile Gln Val Ser Ser Gly Leu Gly Asn Gln Met Phe Gln
1 5 10 15
Tyr Ala Leu Tyr Lys Lys Ile Ser Leu Asn Asp Asn Asp Val Phe Leu
20 25 30
Asp Ser Ser Thr Ser Tyr Met Met Tyr Lys Asn Gln His Asn Gly Tyr
35 40 45
Glu Leu Glu Arg Ile Phe His Ile Lys Pro Arg His Ala Gly Lys Glu
50 55 60
Ile Ile Asp Asn Leu Ser Asp Leu Asp Ser Glu Leu Ile Ser Arg Ile
65 70 75 80
Arg Arg Lys Leu Phe Gly Ala Lys Lys Ser Met Tyr Val Glu Leu Lys
85 90 95
Glu Phe Glu Tyr Asp Pro Ile Ile Phe Glu Lys Lys Glu Thr Tyr Phe
100 105 110
Lys Gly Tyr Trp Gln Asn Tyr Asn Tyr Phe Lys Asp Ile Glu Gln Glu
115 120 125
Leu Arg Lys Asp Phe Val Phe Thr Glu Lys Leu Asp Lys Arg Asn Glu
130 135 140
Lys Leu Ala Asn Glu Ile Arg Asn Lys Asn Ser Val Ser Ile His Ile
145 150 155 160
Arg Arg Gly Asp Tyr Tyr Leu Asn Lys Val Tyr Glu Glu Lys Phe Gly
165 170 175
Asn Ile Ala Asn Leu Glu Tyr Tyr Leu Lys Ala Ile Asn Leu Val Lys
180 185 190
Lys Lys Ile Glu Asp Pro Lys Phe Tyr Ile Phe Ser Asp Asp Ile Asp
195 200 205
Trp Ala Gln Lys Asn Ile Asn Leu Thr Asn Asp Val Val Tyr Ile Ser
210 215 220
His Asn Gln Gly Asn Glu Ser Tyr Lys Asp Met Gln Leu Met Ser Leu
225 230 235 240
Cys Lys His Asn Ile Ile Ala Asn Ser Thr Phe Ser Trp Trp Gly Ala
245 250 255
Phe Leu Asn Asn Asn Asp Asp Lys Ile Val Val Ala Pro Lys Lys Trp
260 265 270
Ile Asn Ile Lys Gly Leu Glu Lys Val Glu Leu Phe Pro Glu Asn Trp
275 280 285
Ile Thr Tyr
290
<210> 12
<211> 876
<212> DNA
<213> Bacillus cereus
<400> 12
atgaagatta ttcaggtgtc ttctggcctg ggcaatcaga tgtttcagta cgcactgtac 60
aagaaaattt ctctgaatga taatgatgtt tttctggact catcaacttc ttatatgatg 120
tacaaaaatc agcataatgg ttatgaactg gaaagaattt ttcatatcaa gccacgtcac 180
gcaggcaagg agattatcga taacctgtca gacctggact cagagctgat ctctcgtatc 240
cgtcgtaagc tgttcggcgc taaaaaatct atgtacgtgg aactgaaaga atttgaatat 300
gatccaatta tttttgagaa aaaagaaact tatttcaaag gttactggca gaactacaat 360
tattttaagg atattgaaca ggaattacgt aaagattttg tttttactga aaaattagat 420
aaaagaaatg aaaaactggc taacgaaatt agaaataaaa attcagtttc aattcacatt 480
agaagaggtg attattatct gaataaagtt tatgaggaaa aatttggtaa tattgcaaat 540
ctggaatatt atctgaaagc tattaatctg gttaaaaaga aaatcgaaga tccaaaattt 600
tatatttttt cagatgatat tgattgggct cagaaaaata ttaatctgac taatgatgtg 660
gtgtatattt ctcataacca gggtaacgag tcatacaagg acatgcagct gatgtctctg 720
tgcaaacata atattattgc taactctact ttctcttggt ggggcgcttt cctgaacaat 780
aatgacgaca aaattgtggt tgctcctaaa aaatggatta atatcaaagg tctggaaaaa 840
gttgaactgt ttccagaaaa ttggattact tattga 876
<210> 13
<211> 281
<212> PRT
<213> Bacteroides eggerthii
<400> 13
Met Arg Leu Ile Lys Met Thr Gly Gly Leu Gly Asn Gln Met Phe Ile
1 5 10 15
Tyr Ala Phe Tyr Leu Arg Met Lys Lys Arg His Thr Asn Thr Arg Ile
20 25 30
Asp Leu Ser Asp Met Met His Tyr Asn Val His His Gly Tyr Glu Met
35 40 45
His Arg Val Phe Asn Leu Pro Lys Thr Glu Phe Cys Ile Asn Gln Pro
50 55 60
Leu Lys Lys Val Ile Glu Phe Leu Phe Phe Lys Lys Ile Tyr Glu Arg
65 70 75 80
Lys Gln Asp Pro Ser Ser Leu Leu Pro Phe Asp Lys Lys Tyr Leu Trp
85 90 95
Pro Leu Leu Tyr Phe Lys Gly Phe Tyr Gln Ser Glu Arg Phe Phe Ala
100 105 110
Asp Met Glu Asn Asp Ile Arg Ile Ala Phe Thr Phe Asn Ser Asp Leu
115 120 125
Phe Asn Glu Lys Thr Gln Ala Met Leu Thr Gln Ile Lys His Asn Glu
130 135 140
His Ala Val Ser Leu His Ile Arg Arg Gly Asp Tyr Leu Glu Pro Lys
145 150 155 160
His Trp Lys Thr Thr Gly Ser Val Cys Gln Leu Pro Tyr Tyr Leu Asn
165 170 175
Ala Ile Thr Glu Met Asn Lys Arg Ile Glu Gln Pro Ser Tyr Tyr Val
180 185 190
Phe Ser Asp Asp Ile Ala Trp Val Lys Glu Asn Leu Pro Leu Pro Gln
195 200 205
Ala Val Phe Ile Asp Trp Asn Lys Gly Ala Glu Ser Trp Gln Asp Met
210 215 220
Met Leu Met Ser His Cys Arg His His Ile Ile Cys Asn Ser Thr Phe
225 230 235 240
Ser Trp Trp Gly Ala Trp Leu Asn Pro Arg Glu Asn Lys Thr Val Ile
245 250 255
Met Pro Glu Arg Trp Phe Gln His Cys Asp Thr Pro Asn Ile Tyr Pro
260 265 270
Asp Gly Trp Ile Lys Val Pro Val Asn
275 280
<210> 14
<211> 846
<212> DNA
<213> Bacteroides eggerthii
<400> 14
atgagactga ttaaaatgac aggcggcctg ggcaaccaaa tgtttatcta cgctttctat 60
ctacgaatga aaaaacgtca tacaaatact cggatcgatt tgtccgacat gatgcattac 120
aacgtccacc atggttatga aatgcaccgc gtgttcaatc ttcccaaaac agaattctgt 180
atcaaccaac ctttgaaaaa ggttatagaa tttcttttct tcaagaaaat ctatgaacgc 240
aaacaagacc catcaagtct cctcccattc gataaaaaat acttatggcc tttgctatac 300
tttaaaggat tctatcagtc ggaaaggttc tttgccgata tggaaaatga catacgtata 360
gcctttacat tcaactcaga cctgttcaat gagaagaccc aagcaatgct aacgcaaata 420
aagcataacg agcatgccgt ttcactacat atccgccggg gagattattt agaacccaaa 480
cattggaaaa caacaggcag tgtgtgccaa ctgccctatt acctcaatgc tattaccgaa 540
atgaacaaac ggatagagca gccttcctat tatgtttttt cggatgacat agcctgggta 600
aaggaaaacc taccgttgcc acaggccgtc ttcattgatt ggaataaagg tgcagaaagc 660
tggcaggaca tgatgctgat gagccattgc cgccaccaca tcatttgcaa cagtacgttt 720
agctggtggg gggcatggtt gaaccccaga gagaataaga cggtaattat gcccgaacgt 780
tggtttcaac attgtgatac gcccaacatc tatcctgacg gttggataaa agtacccgtt 840
aactga 846
<210> 15
<211> 290
<212> PRT
<213> Bacteroides uniformis
<400> 15
Met Lys Ile Val Leu Pro Cys Trp Gly Leu Gly Asn Val Met Phe Gln
1 5 10 15
Tyr Ala Phe Leu Cys Glu Leu Arg Phe Arg Gly Arg Glu Ala Cys Cys
20 25 30
Phe Leu Leu His Lys Lys Leu Arg Phe Glu His Asn Gly Tyr Glu Leu
35 40 45
Asp Lys Leu Phe Lys Val His Pro Tyr Lys Gly Leu Asn Ile Phe Gln
50 55 60
Arg Ile Tyr Ile Arg Leu Val Glu Phe Leu Gly Ala Met Glu Leu Pro
65 70 75 80
Tyr Phe Lys Leu Ile Ser Leu Phe Phe Lys Glu Val Ser Val Lys Glu
85 90 95
Asn Phe Ile Tyr Tyr Asp Glu Val Phe Gln His Pro His Glu Asn Cys
100 105 110
Tyr Phe Lys Gly Thr Trp Gln Ser Pro Leu Tyr Phe Val His Ala Lys
115 120 125
Gln Glu Ile Leu Asp Thr Phe Arg Phe Asp Lys Arg Met Ile Ser Ser
130 135 140
Tyr Thr Arg Asp Val Leu Asn Gln Ile Glu Lys Thr Pro Asn Ser Val
145 150 155 160
Ser Leu His Val Arg Arg Gly Asp Tyr Leu Lys Pro Asp Phe Glu Gly
165 170 175
Leu Ser Lys Cys Cys Pro Asn Asp Tyr Phe Glu Arg Ala Ile Gln Tyr
180 185 190
Met Lys Glu His Met Asp Thr Pro Val Phe Tyr Val Phe Ser Asp Asp
195 200 205
Met Asp Tyr Val Lys Glu Asn Ile Lys Leu Glu Asp Ala Phe Tyr Ile
210 215 220
Asp Gly Asn Arg Gly Asn Asp Ser Trp Gln Asp Met Phe Leu Met Ser
225 230 235 240
Ser Cys Asn His Asn Ile Ile Ala Asn Ser Thr Phe Ser Trp Trp Ser
245 250 255
Ala Phe Leu Asn Ser His Asp Asn Lys Ile Val Ile Ala Pro Lys Arg
260 265 270
Trp Trp Tyr Tyr Phe Glu Thr Asp Asp Val Val Pro Glu Glu Trp Ile
275 280 285
Arg Met
290
<210> 16
<211> 873
<212> DNA
<213> Bacteroides uniformis
<400> 16
atgaaaatag tattgccatg ttggggatta ggaaatgtta tgtttcagta cgcattttta 60
tgtgaactgc gttttagagg aagagaagct tgttgtttct tattacataa aaaattacgt 120
tttgaacata atggatatga gcttgataaa ttgtttaaag tacatcctta taaaggactt 180
aatattttcc aaaggatata tatacgttta gtagagttct tgggggctat ggaattacct 240
tattttaaat taatcagcct tttctttaaa gaggtaagtg ttaaagaaaa ttttatatat 300
tatgatgagg tatttcaaca tccacatgaa aattgctatt ttaaaggaac ttggcagagt 360
cctttgtatt ttgttcatgc caagcaagag atattggata catttcgatt tgacaaaaga 420
atgatttctt cttatacaag agatgtttta aaccaaatag aaaagactcc taacagtgta 480
agtttgcatg tacgtcgcgg tgattatttg aaaccagatt ttgaaggatt gagtaaatgt 540
tgtcctaacg attattttga aagggcaatt caatatatga aagagcatat ggataccccg 600
gttttctatg tcttttctga tgatatggat tatgtgaagg aaaatataaa gttggaagac 660
gctttctata ttgatggtaa tagggggaat gattcttggc aagatatgtt tctaatgagt 720
tcatgcaatc ataatattat agctaattct acatttagtt ggtggagtgc ttttcttaat 780
tcccatgaca ataaaattgt tattgcacca aaacgctggt ggtattattt tgagacggat 840
gatgttgtac cggaagaatg gataagaatg tga 873
<210> 17
<211> 313
<212> PRT
<213> Neocallimastix californiae
<400> 17
Met Lys Ile Leu Ile Phe Ser Val Ser Phe Ser Phe Phe Tyr Leu Leu
1 5 10 15
His Leu Phe Phe Ile Leu Tyr Tyr Ile Ile Ser Lys Ala Ser Lys Glu
20 25 30
Ile Arg Ile Val Lys Leu Cys Gly Gly Leu Gly Asn Gln Met Phe Gln
35 40 45
Tyr Ala Tyr Gly Lys Ser Leu Glu His Lys Leu Gln Glu Lys Val Leu
50 55 60
Phe Asp Val Ser Trp Tyr Lys Tyr Leu Asn Lys Lys Lys Asn Glu Lys
65 70 75 80
Leu Thr Lys Arg Glu Tyr Gly Leu Gly Ile Phe Asn Leu Lys Ile Ser
85 90 95
Phe Pro Thr Lys Lys Gln Leu Lys Lys Cys Asn Asn Lys Thr Phe Glu
100 105 110
Lys Lys Ser Tyr Ile Tyr Asp Glu Glu Leu Leu Gln Asn Lys Gly Ser
115 120 125
Ser Tyr Tyr Val Gly Tyr Phe Gln Asn Glu Lys Tyr Phe Lys Asp Ile
130 135 140
Lys Asp Asn Ile Lys Lys Ile Tyr Thr Phe Pro Lys Ile His Asp Thr
145 150 155 160
Asp Lys Phe Asn Gln Gln Trp Ile Asn Lys Ile Lys Asn Val Lys Asn
165 170 175
Ser Val Phe Ile His Ile Arg Arg Ala Asp Tyr Ile Tyr Leu Asp Gly
180 185 190
Trp Val Leu Ser Met Asp Tyr Tyr Lys Lys Ala Ile Glu Tyr Ile Lys
195 200 205
Lys Asn Val Glu Asn Pro Thr Phe Phe Ile Phe Cys Tyr Gln Cys Lys
210 215 220
Asp Tyr Val Glu Glu Gln Phe Lys Leu Asp Asp Thr Ile Gln Phe Ile
225 230 235 240
Gly Glu Thr Asn Ser Ile Asn Asn Glu Asn Trp Lys Asp Met Val Leu
245 250 255
Met Lys Glu Cys Lys Tyr Ala Ile Ile Ala Asn Ser Ser Phe Ser Trp
260 265 270
Trp Ala Ala Trp Leu Gly Arg Ala Asn Glu Glu Gly Ile Val Ile Ala
275 280 285
Pro Ser Pro Phe Ile Lys Asn Asn Asp Glu Ile Ile Cys Asp Asn Trp
290 295 300
Ile Lys Ile Asn Ser Asn Asn Ser Ser
305 310
<210> 18
<211> 942
<212> DNA
<213> Neocallimastix californiae
<400> 18
atgaaaatat taatattctc tgtttctttt tcctttttct atttattaca tttatttttc 60
atactttact atattatttc taaagcatcc aaagaaataa gaatagtaaa actatgtgga 120
ggtttaggaa atcaaatgtt tcaatatgct tatgggaaat ctcttgaaca caaattacaa 180
gaaaaggtat tatttgatgt ttcatggtat aaatatttga ataaaaagaa aaatgaaaaa 240
ttaactaaaa gggaatatgg attgggtata tttaatttaa aaatatcttt tcctactaaa 300
aaacaactaa aaaaatgtaa taataaaaca tttgaaaaga agagttacat atatgatgaa 360
gaattattac aaaataaagg atcatcgtat tatgtgggat attttcaaaa tgaaaaatat 420
tttaaagata ttaaagataa tataaaaaaa atatatacat ttccaaaaat tcatgatact 480
gataaattta atcaacaatg gataaataaa ataaaaaacg tcaaaaattc cgtctttatt 540
catatcagaa gagcagatta tatatattta gatggatggg ttctttcaat ggattattat 600
aaaaaggcaa ttgagtatat aaaaaaaaat gtagaaaatc ctacattttt catattttgt 660
taccaatgta aagattatgt tgaagagcaa ttcaaattag atgatacaat tcagtttata 720
ggagaaacaa attcaattaa taatgaaaat tggaaagata tggttttaat gaaggaatgt 780
aaatatgcaa taatagcaaa ttcatcattt agttggtggg cagcatggct tggaagagcc 840
aatgaagaag gcattgtaat tgctccttct ccatttatta aaaataatga tgaaataata 900
tgtgataatt ggattaaaat taatagtaat aattcttcat ag 942

Claims (10)

1.一株高产2’-岩藻糖基乳糖的酿酒酵母工程菌株,其特征在于,所述酿酒酵母工程菌株中含有重组的乳糖透性酶(Lactose permease)、重组的GDP-甘露糖脱水酶(GDP-mannose-4,6-dehydratase)、重组的GDP-岩藻糖合酶(GDP-L-fucose synthase)以及重组的α-1,2-岩藻糖基转移酶(α-1,2fucosyltransferase)。
2.根据权利要求1所述的酿酒酵母工程菌株,其特征在于,所述α-1,2-岩藻糖基转移酶来源于蜡样芽孢杆菌(Bacillus cereus);优选的,所述α-1,2-岩藻糖基转移酶的氨基酸序列如SEQ ID No.11所示。
3.根据权利要求1所述的酿酒酵母工程菌株,其特征在于,所述乳糖透性酶来源于乳酸克鲁维斯酵母;优选的,所述乳糖透性酶的氨基酸序列如SEQ ID No.1所示。
4.根据权利要求1所述的酿酒酵母工程菌株,其特征在于,所述GDP-甘露糖脱水酶来源于大肠杆菌;优选的,所述GDP-甘露糖脱水酶的氨基酸序列如SEQ ID No.3所示。
5.根据权利要求1所述的酿酒酵母工程菌株,其特征在于,所述GDP-岩藻糖合酶来源于大肠杆菌;优选的,所述GDP-岩藻糖合酶的氨基酸序列如SEQ ID No.5所示。
6.根据权利要求1-5任一所述的酿酒酵母工程菌株,其特征在于,所述酿酒酵母工程菌株的出发菌株为酿酒酵母W303-1a。
7.权利要求1-6任一所述的酿酒酵母工程菌株的制备方法,其特征在于,所述方法包括将所述目的基因重组到酿酒酵母中的步骤。
8.根据权利要求7所述的方法,其特征在于,所述方法包括将所述目的基因整合到酿酒酵母的基因组中的步骤。
9.根据权利要求8所述的方法,其特征在于,所述目的基因的整合位点包括TRP1、URA3或LEU2。
10.权利要求1-6任一所述的酿酒酵母工程菌株在生产2’-岩藻糖基乳糖中的应用。
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CN113502297A (zh) * 2021-06-11 2021-10-15 华南理工大学 一种合成鸟苷二磷酸岩藻糖的重组毕赤酵母及其构建方法与应用
CN113528480A (zh) * 2021-07-07 2021-10-22 上海交通大学 一种α-1,2-岩藻糖基转移酶突变体及其构建方法和应用
CN114634883A (zh) * 2022-05-17 2022-06-17 中国海洋大学 产2′-岩藻糖基乳糖的重组工程菌及其构建方法与应用
WO2024067774A1 (zh) * 2022-09-28 2024-04-04 山东大学 一种提高基因表达水平的酿酒酵母工程菌及其构建方法与应用

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