CN113817698B - 一种朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶及其应用 - Google Patents

一种朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶及其应用 Download PDF

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CN113817698B
CN113817698B CN202111098375.2A CN202111098375A CN113817698B CN 113817698 B CN113817698 B CN 113817698B CN 202111098375 A CN202111098375 A CN 202111098375A CN 113817698 B CN113817698 B CN 113817698B
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周景文
余世琴
陈坚
曾伟主
高松
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Abstract

本发明公开了一种朝鲜淫羊藿来源的黄酮8‑异戊烯基转移酶及其应用,属于基因和代谢工程领域。本发明筛选获得了朝鲜淫羊藿来源的EkF8DT3,并构建了表达该酶的重组酿酒酵母。该重组酿酒酵母具有催化山奈酚合成8‑异戊烯基山奈酚的能力,在250mL摇瓶进行发酵,外源添加200mg/L的山奈酚,可以获得118.3mg/L的8‑异戊烯基山奈酚,较已报道的EsPT2增产356.8%,对于推动高产淫羊藿素在工业中的应用具有重要意义。

Description

一种朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶及其应用
技术领域
本发明涉及一种朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶及其应用,属于基因和代谢工程领域。
背景技术
淫羊藿素是中药淫羊藿的主要药用成分之一,属于高附加值黄酮类化合物。淫羊藿素的合成需要一个重要的基因:异戊烯基转移酶(prenyltransferase,PT)的催化才能合成。但是近十年来仅有9个异戊烯基转移酶被报道。2008年,Sasaki等克隆表达了第一个植物苦参(Sophora flavescens)来源的黄酮异戊烯基转移酶SfN8DT。此后,Akashi等克隆得到了催化大豆抗毒素4位异戊烯基化的GmG4DT26,Sasaki等得到的SfG6DT和Shen等得到的LaPT1分别作用于染料木素的6位和3′位,Karamat等获得的PcPT催化7-羟基香豆素发生6位和8位异戊烯基化。然而,除SfN8DT外,上述获得的异戊烯基转移酶,催化底物仅为异黄酮或者香豆素,无法特异性的催化黄酮母核柚皮素的异戊烯基化。最近报道了一个来源于箭叶淫羊藿(Epimedium sagittatum)的异戊烯基转移酶EsPT2可以催化山奈酚获得8-异戊烯基山奈酚,但是产量仅25.9mg/L。因此。对新型、高效且特异性催化黄酮8位异戊烯化的异戊烯基转移酶对微生物法合成高附加值淫羊藿素具有重要意义。
异戊烯基转移酶广泛存在于生物界,参与6万种以上天然产物的合成。植物是巨大的异戊烯基转移酶基因库。其中朝鲜淫羊藿(Epimedium koreanum Nakai)作为淫羊藿的道地药材,药用价值高,对其相关异戊烯基转移酶的研究具有重要的学术和经济意义。
发明内容
本发明提供了朝鲜淫羊藿来源的潜在黄酮8-异戊烯基转移酶(Flavonoid8-Dimethylallyltransferase,F8DT),为(a)或(b):
(a)由SEQ ID NO.3所示的氨基酸序列组成的蛋白质;
(b)在(a)限定的氨基酸序列中经过取代、缺失或添加一个或几个氨基酸且具有黄酮8-异戊烯基转移酶活性的由(a)衍生的蛋白质。
本发明还提供了编码所述黄酮8-异戊烯基转移酶的基因。
在一种实施方式中,所述基因具有如SEQ ID NO.8所示的核苷酸序列。
本发明还提供一种表达载体,所述的表达载体携带SEQ ID NO.8所示的核苷酸序列。
本发明提供一种含有所述基因或表达所述8-异戊烯基转移酶的微生物细胞。
本发明还提供了含有所述基因或所述表达载体的微生物细胞。
在一种实施方式中,所述微生物细胞的基因组上整合了SEQ ID NO.8所示的基因。
在一种实施方式中,所述微生物细胞中含有携带所述基因的重组质粒。
在一种实施方式中,所述微生物细胞为酿酒酵母菌株C800(CEN.PK2-1D;MATα;ura3-52;leu2-3,112;trp1-289;his3Δ1;MAL2-8C;SUC2;gal80::KanMX)(公开于论文Gao,S.;Zhou,H.;Zhou,J.,et al.,Promoter-library-based pathway optimization forefficient(2S)-naringenin production from p-coumaric acid in Saccharomycescerevisiae[J].J Agric Food Chem 2020,68(25),6884-6891.)。
在一种实施方式中,所述重组质粒为pY26-PGAL7-EGFP(公开于论文Gao,S.;Xu,X.Y.;Zeng,W.Z.,et al.,Efficient biosynthesis of(2S)-eriodictyol from(2S)-naringenin in Saccharomyces cerevisiae through a combination of promoteradjustment and directed evolution[J].ACS Synth Biol 2020,9(12),3288-3297.)。
在一种实施方式中,所述重组微生物细胞是以酿酒酵母菌株C800为宿主,表达SEQID NO.3所示的8-异戊烯基转移酶或含有连接了SEQ ID NO.8所示基因的重组质粒。
本发明提供了构建所述重组微生物细胞的方法,所述方法是将SEQ ID NO.3所示的基因连接至pY26-PGAL7-EGFP中EGFP基因所在位置,替换EGFP基因,再将重组质粒转入酿酒酵母C800中,构建得到重组酿酒酵母。
在一种实施方式中,所述表达载体是将SEQ ID NO.8所示的核苷酸序列连接至常用质粒pET28a(+)中BamHI和HindIII之间的位置,再将重组质粒转入到大肠杆菌BL21(DE3)中,构建得到重组大肠杆菌。
本发明还提供了一种产EkF8DT3酶的方法,是将所述大肠杆菌接种至TB培养基中,于35~40℃培养至OD600为0.04~0.06,加入终浓度为0.01~1mM的IPTG,于28~30℃诱导表达至少8h。
本发明还提供一种生产8-异戊烯基山奈酚的方法,是将所述重组酿酒酵母接种至含山奈酚的培养基中,将山奈酚转化为8-异戊烯基山奈酚。
在一种实施方式中,所述方法是将所述重组酿酒酵母接种至培养基中培养,并在接种后每10~14h加入底物山奈酚,培养至少72h。
在一种实施方式中,所述方法是将每0.6mg的EkF8NDT3酶添加到含172.6μM山奈酚的反应体系中,30℃反应至少1h。
本发明还提供所述重组酿酒酵母在制备微生物细胞催化剂方面的应用。
本发明还提供所述重组酿酒酵母在生产含8-异戊烯基山奈酚的医用营养品或药物中的应用。
本发明的有益效果:本发明筛选和验证的8-异戊烯基转移酶及EkF8DT3基因,较已报道的EsPT2,在酿酒酵母中表达,可以合成更多的8-异戊烯基山奈酚。在250mL摇瓶进行发酵,外源添加200mg/L的山奈酚,可以获得118.3mg/L的8-异戊烯基山奈酚,较已报道的在酿酒酵母中最高产量25.9mg/L,增产356.8%。高产8-异戊烯基山奈酚菌株的获得对于推动高产淫羊藿素在工业中的应用具有重要意义。
附图说明
图1为山奈酚经过EkF8DT3催化产8-异戊烯基山奈酚示意图。
图2为验证EkF8DT3催化能力的高效液相结果;山奈酚标准品的出峰时间为16.376min,8-异戊烯基山奈酚标准品的出峰时间为22.544min。
图3为验证EkF8DT3催化能力的液相-质谱联用结果。A1:山奈酚标准品和8-异戊烯基山奈酚标准品在液质-质谱联用中液相结果;山奈酚标准品和8-异戊烯基山奈酚标准品的出峰时间分别为8.70min和10.03min;A2:山奈酚标准品的质谱结果,山奈酚在负离子模式下出现285.0336的离子峰;A3:8-异戊烯基山奈酚标准品的质谱结果,8-异戊烯基山奈酚在负离子模式下出现353.0894的离子峰;B1:实施例3表达EkF8DT3的酿酒酵母发酵液在液相-质谱联用中的液相结果,在对应时间有山奈酚和8-异戊烯基山奈酚目标峰;B2:实施例3表达EkF8DT3的酿酒酵母发酵液中的底物山奈酚在质谱的检测结果,可以看到对应离子峰出现,与标准品山奈酚一致;B3:实施例3表达EkF8DT3的酿酒酵母发酵液中8-异戊烯基山奈酚的质谱检测结果,可以看到对应离子峰出现,与标准品8-异戊烯基山奈酚一致。
图4为EkF8DT3的酶促反应动力学曲线。
具体实施方式
YNB培养基:0.72g/L酵母氮源基础培养基、20g/L葡萄糖、50mg/L亮氨酸、50mg/L色氨酸、50mg/L组氨酸。
YPD培养基:10g/L酵母粉、20g/L蛋白胨、20g/L葡萄糖。
TB培养基:24g/L酵母粉、12g/L蛋白胨、4mL/L甘油。
固体培养基中添加20g/L的琼脂粉。
缓冲液A:20mM K2HPO4,20mM KH2PO4,50mM NaCl,pH 7.4。
缓冲液B:20mM K2HPO4,20mM KH2PO4,50mM NaCl,500mM咪唑,pH 7.4。
PBS缓冲液:160mL的20mM NaH2PO4与840mL的20mM Na2HPO4混合(pH 7.5)。
山奈酚、8-异戊烯基山奈酚的检测方法:
样品使用岛津高效液相检测(Prominence LC-20A instrument),C18反相色谱柱(4.6mm×250mm,Thermo),柱温25℃。流动相为乙腈(A):水(B),并添加1‰的三氟乙酸。流速1mL/min,进样量10μL,检测波长为350nm。流动相条件为0-10min(B:10-40%),10-30min(B:40-80%),30-35min(B:80%),35-37min(B:80-10%),37-40min(B:10%)。山奈酚标样出峰时间为16.376min,8-异戊烯基山奈酚出峰时间为22.544min。
8-异戊烯基转移酶的酶活测定方法:
取600μL酶液于1.5mL离心管中,依次加入200μL溶于PBS中且浓度为5mM的二甲烯丙基焦磷酸(DMAPP)、200μL溶于PBS中且浓度为1mM的山奈酚(94.7U/g)。使用移液器充分混匀后置于30℃水浴锅孵育1h后取出。吸取500μL反应液与500μL的乙酸乙酯混合,充分震荡混匀后,14000rpm离心5min,取上层乙酸乙酯过0.22μm尼龙膜后使用高效液相色谱检测产物8-异戊烯基山奈酚的生成。
定义在pH7.5的PBS缓冲液,30℃条件下,每分钟催化1μmol的底物山奈酚转化为产物8-异戊烯基山奈酚所需的酶量为1个酶活单位(1U)。
实施例1:EkF8DT基因的筛选
以已知功能的SfN8DT(Sophora flavescens,NCBI蛋白质登录号GI(Geninfoidentifier):GI:169658914)的氨基酸序列为模板,通过tBLASTn(Lv,Y.et al.,Spatialorganization of silybin biosynthesis in milk thistle[Silybum marianum(L.)Gaertn].2017,Plant J 92(6),995–1004),从淫羊藿RNA-seq数据库中预测到5条潜在的同源基因,依次对应c213652、c203632、c218750、c198229和c203562,分别被命名为EkF8DT1、EkF8DT2、EkF8DT3、EkF8DT4和EkF8DT5,原始核苷酸序列如序列表SEQ ID NO.1、SEQ IDNO.2、SEQ ID NO.3、SEQ ID NO.4和SEQ ID NO.5中所示,分别对序列进行优化后获得SEQID NO.6、SEQ ID NO.7、SEQ ID NO.8、SEQ ID NO.9和SEQ ID NO.10所示,对应的氨基酸序列如序列表SEQ ID NO.11、SEQ ID NO.12、SEQ ID NO.13、SEQ ID NO.14和SEQ ID NO.15中所示。
本发明中tBLASTn的预测序列及评分见表1,预测的序列在朝鲜淫羊藿不同组织中的分布见表2,菌株和质粒的基因型见表3。
表1tBLASTn预测序列及评分
*:SfN8DT作为tBLASTn的模板
表2预测的序列在朝鲜淫羊藿不同组织中的分布*
*:其中的数字代表RNA-Seq结果中各个基因的FPKM值(Fragments Per Kilobaseof exon model per Million mapped fragments,即每千个碱基的转录在每百万映射读取的数值),用于表征特定基因的丰度,数值越大,表示基因的丰度越高。
表3菌株和质粒的基因型
实施例2:表达朝鲜淫羊藿F8NDT的重组菌株的构建
(1)重组质粒的构建
将合成的如SEQ ID NO.6~10所示基因分别整合在pY26-PGAL7-EGFP中,将SEQ IDNO.6~10所示基因分别完全取代EGFP的DNA序列,并使用强启动子PGAL7起始转录,依次获得重组质粒pY26-EkN8DT1、pY26-EkN8DT2、pY26-EkN8DT3、pY26-EkN8DT4和pY26-EkN8DT5。
将合成的基因SEQ ID NO.8所示基因分别整合在pET28a(+)的BamHI/HindIII位置处,获得质粒pET28-EkF8DT3。
(2)重组酿酒酵母和重组大肠杆菌的构建
通过酿酒酵母的高效转化方法,将步骤(1)构建的重组质粒pY26-EkN8DT1、pY26-EkN8DT2、pY26-EkN8DT3、pY26-EkN8DT4和pY26-EkN8DT5分别转化到酿酒酵母菌株C800中,将转化液涂布在YNB固体平板上,30℃培养3-5天直至长出单菌落,即为重组菌。依次将重组菌命名为C800FT1、C800FT2、C800FT3、C800FT4和C800FT5。
通过大肠杆菌的化学转化方法,将步骤(1)中构建的重组质粒pET28-EkF8DT3转化到大肠杆菌BL21(DE3)中,获得重组大肠杆菌EFT3。
实施例3:表达朝鲜淫羊藿F8NDT的重组酿酒酵母菌株生产淫羊藿素
将实施例2构建的重组酿酒酵母菌株用于发酵验证,以柚皮素、二氢山奈酚、芹菜素、山奈酚和山奈素等5种化合物为底物添加到发酵液中,检测有无底物消耗和新物质生成。
分别将菌株C800NT1、C800NT2、C800NT3、C800NT4和C800NT5在250mL摇瓶中发酵,具体步骤为:挑取至少10个单菌落接种在含有20mL YNB液体培养基的250mL摇瓶中,30℃,220rpm培养16-18h,获得种子培养基。将种子培养基以2%(V/V)转接到含有20mL新鲜YPD液体培养基的250mL摇瓶中,在第12、24、36和48h时,分别向培养基中添加50mg/L的山奈酚,累计共添加200mg/L的山奈酚,30℃,220rpm培养72小时后结束发酵。
取500μL的发酵液于2mL的破碎管中,13500rpm离心5min,去上清液。将菌体沉淀添加0.5mm玻璃珠和500μL的乙酸乙酯,使用MP震荡破碎仪破碎细胞,按照推荐程序震荡8-10个循环,每个循环40s。将破碎液13500rpm离心5min后,使用尼龙膜过滤后备用检测。结果显示,重组酿酒酵母菌株经过72h发酵后(此时菌体OD600约为80),可以催化200mg/L的山奈酚,获得118.3mg/L的8-异戊烯基山奈酚,转化率为47.8%。
实施例4:EkF8NDT酶学性质检测
将实施例2构建的重组大肠菌株EFT3单菌落接种在含有25mL LB培养基的250mL摇瓶中,培养基中添加终浓度为50g/mL的卡那霉素,37℃,220rpm培养10-12h后,按照起始OD600=0.01转接到含有50mL新鲜TB培养基的250mL摇瓶中,培养基中添加终浓度为50μg/mL的卡那霉素,37℃,220rpm培养3-4h后,待OD600达到2-3之间时,添加终浓度为1mM的IPTG进行诱导表达,同时将温度降低为30℃。诱导表达8h后,将发酵液于4℃,5000rpm离心10min后去除上清液,沉淀使用50mL PBS缓冲液重悬2次后,4℃,5000rpm离心10min去除上清液。沉淀使用50mL的PBS重悬后加入已经预冷到4℃的高压均质机中。将高压均质机调节为850bar,开机并破碎2次后收集裂解液。裂解液4℃,14000rpm离心10min保留上清液。上清液过0.45μm的滤膜备用。过滤液即为粗酶液。
使用亲和层析法回收带有His标签的EkF8DT3蛋白质。使用缓冲液A平衡1mL镍柱,然后以1mL/min流速上粗酶液,以1mL/min流速冲洗10个镍柱体积的缓冲液A,随后以1mL/min流速使用缓冲液B冲洗镍柱,根据UV值收集洗脱峰。将收集到的洗脱峰使用脱盐柱(Hitrap Desalting,5mL)进行脱盐处理,用pH 7.5的PBS以5mL/min的流速洗脱回收目标蛋白。使用NanoDrop对回收的目标蛋白进行定量,并用pH 7.5的PBS稀释到1mg/mL置于4℃冰上备用。
经过检测600μL粗酶液的酶活约5.4U,8-异戊烯基山奈酚的浓度为61.2mg/L(172.6μM),转化率为86.3%。体外催化酶促反应进一步验证了EkF8DT3的催化底物为山奈酚,产物为8-异戊烯基山奈酚。经检测,EkF8DT3的Vmax、Km、kcat和Kcat/Km依次为9.04μM/(min·mg)、177.09μmol/L、6.48/s和0.0366μmol/(L·s)。
虽然本发明已以较佳实施例公开如上,但其并非用以限定本发明,任何熟悉此技术的人,在不脱离本发明的精神和范围内,都可做各种的改动与修饰,因此本发明的保护范围应该以权利要求书所界定的为准。
SEQUENCE LISTING
<110> 江南大学
<120> 一种朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶及其应用
<130> BAA210494A
<160> 15
<170> PatentIn version 3.3
<210> 1
<211> 407
<212> PRT
<213> Epimedium koreanum Nakai
<400> 1
Met Asp Ser Leu Leu Leu Leu Gly Ser Val Ser Lys Pro Cys Trp Arg
1 5 10 15
Leu Ser Phe Ser Ala Ser Ala Lys Leu Ser Thr Ala Thr Arg Gly Tyr
20 25 30
His Val Pro Ile Arg Phe Ala Asn Ser Ser Ala Trp Ser Thr Gln Glu
35 40 45
Arg Arg Tyr Phe Gly Gln Leu Gln Gly His Leu Ile Asn His His Ile
50 55 60
Thr Ile Asp Ala Glu Lys Ser Ser Phe Tyr Arg Arg Ala Asp Lys Lys
65 70 75 80
Gly Leu Val Asn Ala Thr Ser Glu Pro Pro Phe Ala Ser Glu Pro Glu
85 90 95
Ser Tyr Asn Pro Asn Asn Phe Trp Arg Ser Met Gln Ser Ala Thr Asp
100 105 110
Ala Phe Tyr Arg Phe Ser Arg Pro His Thr Val Ile Gly Thr Ala Leu
115 120 125
Ser Ile Leu Ser Val Ser Leu Leu Ala Ile Glu Arg Leu Ser Asp Leu
130 135 140
Ser Pro Leu Phe Phe Thr Gly Leu Leu Glu Ala Ile Val Ala Ala Leu
145 150 155 160
Phe Met Asn Ile Tyr Ile Val Gly Leu Asn Gln Leu Phe Asp Val Glu
165 170 175
Ile Asp Lys Val Asn Lys Pro Tyr Leu Pro Leu Ala Ser Gly Glu Tyr
180 185 190
Ser Ile Gly Thr Gly Ile Leu Ile Val Ala Ala Phe Ala Val Met Ser
195 200 205
Phe Trp Leu Gly Trp Phe Val Gly Ser Gly Pro Leu Leu Trp Ala Leu
210 215 220
Ser Ile Ser Phe Ile Leu Gly Thr Ala Tyr Ser Ile Asn Leu Pro Leu
225 230 235 240
Leu Arg Trp Lys Arg Phe Ala Leu Val Ala Ala Met Cys Ile Leu Val
245 250 255
Val Arg Ala Val Ile Val Gln Leu Ala Phe Phe Leu His Ile Gln Thr
260 265 270
Phe Val Tyr Arg Arg Pro Ala Ile Leu Thr Arg Pro Leu Ile Phe Ala
275 280 285
Thr Ala Phe Met Ser Phe Phe Ser Val Val Ile Ala Leu Phe Lys Asp
290 295 300
Ile Pro Asp Ile Glu Gly Asp Ala Ile Phe Gly Ile Arg Ser Phe Thr
305 310 315 320
Val Arg Leu Gly Gln Lys Arg Val Phe Trp Ile Cys Val Tyr Leu Leu
325 330 335
Glu Met Ala Tyr Gly Val Ala Val Leu Val Gly Ala Ala Ser Pro Ser
340 345 350
Pro Trp Ser Lys Leu Val Thr Val Leu Gly His Val Val Leu Ala Ser
355 360 365
Ile Leu Trp Leu Asn Ala Lys Ser Val Asp Leu Thr Asn Lys Thr Ala
370 375 380
Ile Thr Ser Phe Tyr Met Phe Ile Trp Lys Leu Phe Tyr Ala Glu Tyr
385 390 395 400
Leu Leu Ile Pro Leu Val Arg
405
<210> 2
<211> 397
<212> PRT
<213> Epimedium koreanum Nakai
<400> 2
Met Val Ser Ser Phe Ser Phe Pro Ser Phe Ala Val Thr Lys Tyr Thr
1 5 10 15
Pro Gln Gln Gly Phe Leu Leu Arg Lys Leu Arg Pro Phe Ser Ser Gln
20 25 30
Arg Arg Asp Ala Asp Ile Ala Leu Leu Phe Lys Val Gln Thr Glu Asn
35 40 45
Lys Ile Phe Ser Ala Leu Lys Ser Ser Asp Pro Gln Ser Ser Tyr Asn
50 55 60
Leu Asp Lys Pro Leu Leu Arg His Thr Ser Ser Ile Arg Lys Leu Ser
65 70 75 80
Pro Pro Ala Ala Thr Thr Ser Glu His Glu Asn Val Pro Leu Ser Ser
85 90 95
Leu Ser Lys Ala Ile Asp Ile Phe Phe Arg Phe Ile Arg Pro Tyr Ala
100 105 110
Ile Val Cys Thr Met Phe Gly Ile Met Ser Val Ser Leu Leu Pro Val
115 120 125
Glu Thr Leu Ala Asp Leu Thr Pro Lys Phe Phe Leu Gly Leu Gly Lys
130 135 140
Ala Met Ile Ala Val Val Ser Met Asn Leu Phe Ser Val Ser Val Asn
145 150 155 160
Gln Phe Tyr Asp Val Glu Leu Asp Lys Val Asn Lys Pro Tyr Leu Pro
165 170 175
Leu Ala Ser Gly Glu Leu Ser Met Glu Ala Gly Ala Ala Phe Val Ile
180 185 190
Leu Ala Ser Ser Met Gly Ile Ser Phe Gly Leu Met Leu Gln Ser Pro
195 200 205
Pro Leu Leu Cys Thr Ile Leu Thr Phe Phe Leu Phe Gly Gly Ala Tyr
210 215 220
Ser Ile Asp Leu Pro Phe Leu Arg Trp Lys Lys His Pro Val Leu Ala
225 230 235 240
Val Val Cys Ile Thr Ala Met Arg Gly Leu Ala Leu Gln Leu Gly Val
245 250 255
Phe Phe His Ile Gln Lys Tyr Val Leu Gly Lys Pro Met Ala Leu Thr
260 265 270
Arg Ser Val Val Phe Val Thr Ile Phe Met Cys Val Phe Asn Ile Ala
275 280 285
Ile Ser Leu Ile Lys Asp Leu Pro Asp Val Asp Gly Asp Lys Ala His
290 295 300
Gly Phe Gln Asn Met Thr Ile Arg Phe Gly Lys Glu Lys Val Phe Trp
305 310 315 320
Gly Cys Thr Ser Leu Met Leu Ala Thr Tyr Gly Ala Ala Val Ala Met
325 330 335
Gly Phe Ser Ser Pro Phe Leu Ala Thr Lys Leu Ile Thr Val Ile Ala
340 345 350
His Ser Ala Leu Gly Leu Phe Val Leu Leu Arg Ala Arg Ser Ile Lys
355 360 365
Leu Asp Asp Asp Glu Ser Thr Gln Ser Tyr Tyr Leu Leu Leu Trp Asp
370 375 380
Leu Cys Lys Ile Glu Tyr Leu Leu Ala Pro Phe Val Arg
385 390 395
<210> 3
<211> 391
<212> PRT
<213> Epimedium koreanum Nakai
<400> 3
Met Val Ser Arg Cys Ala Ser Pro Ser Phe Ser Ile Thr Lys Tyr Thr
1 5 10 15
Pro His Gln Gly Ser Leu Leu Thr Ser Leu Lys Pro Phe Ser Ser Gln
20 25 30
Lys Pro Gly Ala Arg Ile Glu Tyr Lys Leu Gln Gln Asn His Ile Phe
35 40 45
Cys Ala Leu Arg Lys Asp Ser His Ala Ser Leu Thr His Thr His Glu
50 55 60
Asn Glu Leu Leu Phe Lys Asp Lys Ser Pro Thr Arg Glu Lys Gly Arg
65 70 75 80
Leu Ser Ala Thr Ser Ser Glu Asn Ala Pro Ser Ser Phe Ser Thr Lys
85 90 95
Leu Asp Met Phe Ile Lys Phe Val Arg Pro Tyr Ala Thr Ile Gly Ile
100 105 110
Ile Gly Asn Thr Ile Cys Met Cys Ile Leu Pro Val Gln Thr Met Ala
115 120 125
Asp Leu Ser Pro Arg Phe Phe Ile Gly Val Ala Gln Ala Ile Ala Ser
130 135 140
Met Val Leu Met Asn Leu Phe Asn Val Ala Val Asn Gln Val Tyr Asp
145 150 155 160
Val Glu Leu Asp Lys Val Asn Lys Pro Tyr Leu Pro Leu Ala Ser Gly
165 170 175
Gly Val Ser Met Thr Ser Ala Thr Leu Phe Thr Ile Leu Thr Ala Ala
180 185 190
Leu Ser Ile Ala Leu Gly Tyr Phe Ser Ser Pro Ala Leu Phe Tyr Gly
195 200 205
Ser Ile Ala Phe Phe Leu Ser Ala Ser Ala Tyr Ser Val Asn Phe Pro
210 215 220
Leu Leu Arg Trp Lys His Asn Ala Leu Gly Ala Ile Ile Ser Leu Met
225 230 235 240
Leu Trp Gly Ile Ser Leu Gln Thr Gly Val Phe Phe His Ile Gln Gln
245 250 255
Tyr Val Leu Gly Lys Pro Met Val Leu Lys Asn Ser Phe Ile Tyr Ala
260 265 270
Ile Ile Phe Gln Ser Leu Phe Ser Ile Val Val Ala Thr Leu Lys Asp
275 280 285
Leu Pro Asp Val Glu Gly Asp Gln Ala Asn Gly Ser Thr Asn Leu Thr
290 295 300
Ile Leu Ile Gly Lys Glu Lys Val Phe Trp Gly Cys Thr Ser Leu Met
305 310 315 320
Leu Ala Thr Tyr Ile Gly Thr Ala Ala Phe Gly Ala Thr Leu Pro Ile
325 330 335
Leu Lys Asn Lys Leu Val Thr Met Val Ala His Ser Ala Leu Ala Val
340 345 350
Phe Leu Trp Leu Gln Ala Lys Gln Ile Asp Leu Ala Asp Asp Ala Ser
355 360 365
Thr Gln Ser Tyr Tyr Leu Leu Met Trp Lys Leu Cys Asn Ile Glu Tyr
370 375 380
Leu Leu Ile Pro Phe Val Gly
385 390
<210> 4
<211> 394
<212> PRT
<213> Epimedium koreanum Nakai
<400> 4
Met Asp Leu Arg Ser Leu Tyr Ser Pro Cys Ser Ala Thr Ser Val Leu
1 5 10 15
Thr Pro His His Gln Lys Ile Leu Thr Ala Lys Pro Thr Val Gln Ser
20 25 30
Ser Lys Ile Ser Phe Lys Phe Ser Ser Ser Ser Ser Ser Leu Thr Thr
35 40 45
Ile Gly Ile Ser His Ser His Asn Ile Lys Ser Ala Pro Val Lys His
50 55 60
Thr Lys Arg Leu Ser Ile Leu Ala Cys Ser Pro Ile Asp Tyr Ala Ala
65 70 75 80
Gly Ser Gly Ser Gly Ser Gly Ser Asp Pro Leu Leu Val Lys Leu Ser
85 90 95
Glu Phe Arg Asp Ala Ser Trp Arg Phe Leu Arg Pro His Thr Ile Arg
100 105 110
Gly Thr Ala Leu Gly Ser Cys Ala Leu Val Ala Arg Ala Leu Val Glu
115 120 125
Asn Thr His Leu Ile Arg Trp Ser Leu Leu Leu Lys Ala Leu Ser Gly
130 135 140
Val Phe Ala Leu Ile Cys Gly Asn Gly Tyr Ile Val Gly Ile Asn Gln
145 150 155 160
Ile Tyr Asp Ile Gly Ile Asp Lys Val Asn Lys Pro Tyr Leu Pro Ile
165 170 175
Ala Ala Gly Asp Leu Ser Val Gln Ser Ala Trp Tyr Leu Val Val Phe
180 185 190
Phe Ala Val Ala Gly Leu Leu Ile Val Ser Phe Asn Phe Gly Thr Phe
195 200 205
Ile Thr Ser Leu Tyr Cys Leu Gly Leu Phe Leu Gly Thr Val Tyr Ser
210 215 220
Val Pro Pro Phe Arg Met Lys Lys Tyr Pro Val Ala Ala Phe Leu Ile
225 230 235 240
Ile Ala Thr Val Arg Gly Phe Leu Leu Asn Phe Gly Val Tyr His Ala
245 250 255
Thr Arg Ala Ala Leu Gly Leu Thr Phe Glu Trp Ser Ser Pro Val Ala
260 265 270
Phe Ile Thr Thr Phe Val Thr Met Phe Ala Leu Val Ile Ala Ile Thr
275 280 285
Lys Asp Leu Pro Asp Val Glu Gly Asp Arg Lys Phe Gln Ile Ser Thr
290 295 300
Leu Ala Thr Thr Leu Gly Val Arg Asn Ile Ala Leu Leu Gly Ser Gly
305 310 315 320
Leu Leu Leu Ala Asn Tyr Leu Gly Ala Ile Phe Ala Ala Val Tyr Met
325 330 335
Pro Gln Ala Phe Arg Ser Ser Leu Met Ile Pro Val His Ala Ile Leu
340 345 350
Leu Leu Ser Leu Ile Phe Gln Ala Trp Ile Leu Glu Arg Ala Asn Tyr
355 360 365
Thr Lys Glu Ala Ile Leu Ala Phe Tyr Arg Phe Ile Trp Asn Leu Phe
370 375 380
Tyr Ala Glu Tyr Ile Val Phe Pro Phe Ile
385 390
<210> 5
<211> 369
<212> PRT
<213> Epimedium koreanum Nakai
<400> 5
Met Ala Thr Leu Leu Asn Thr Leu Ser Leu Ser Ser Ala Lys Leu Thr
1 5 10 15
Asn Arg Arg Thr Gln Ser His Gln Pro Ser Ser Phe Phe Phe Leu Pro
20 25 30
Val Ser Thr Pro Ser Phe Thr Arg Arg Ile Leu Val Val Arg Ala Ala
35 40 45
Glu Thr Asp Thr Asn Glu Val Lys Pro Ser Ser Gly Ser Ser Ile Asn
50 55 60
Gln Leu Leu Gly Ile Lys Gly Ala Ser Gln Glu Thr Asn Lys Trp Lys
65 70 75 80
Ile Arg Leu Gln Leu Met Lys Pro Val Thr Trp Pro Pro Leu Val Trp
85 90 95
Gly Val Val Cys Gly Ala Ala Ala Ser Gly Asn Phe His Trp Asn Val
100 105 110
Glu Asp Val Gly Lys Ser Ile Leu Cys Met Ile Met Ser Gly Pro Cys
115 120 125
Leu Thr Gly Tyr Thr Gln Thr Leu Asn Asp Trp Tyr Asp Arg Glu Ile
130 135 140
Asp Ala Ile Asn Glu Pro Tyr Arg Pro Ile Pro Ser Gly Ala Val Ser
145 150 155 160
Glu Asn Glu Val Thr Thr Gln Ile Trp Val Leu Leu Leu Gly Gly Leu
165 170 175
Gly Leu Ala Gly Leu Leu Asp Val Leu Ala Gly His Asn Phe Pro Ile
180 185 190
Val Phe Tyr Leu Ala Leu Gly Gly Ser Leu Leu Ser Tyr Ile Tyr Ser
195 200 205
Ala Pro Pro Leu Lys Leu Lys Gln Phe Gly Trp Val Gly Asn Phe Ala
210 215 220
Leu Gly Ala Ser Tyr Ile Ser Leu Pro Trp Trp Ala Gly Gln Ala Leu
225 230 235 240
Phe Gly Thr Leu Thr Pro Asp Val Ile Val Leu Thr Leu Leu Tyr Ser
245 250 255
Ile Ala Gly Leu Gly Ile Ala Ile Ile Asn Asp Phe Lys Ser Ile Glu
260 265 270
Gly Asp Arg Ala Leu Gly Leu Gln Ser Leu Pro Val Ala Phe Gly Val
275 280 285
Asp Thr Ala Lys Trp Ile Cys Val Gly Ala Ile Asp Ile Thr Gln Leu
290 295 300
Ser Ile Ala Gly Tyr Leu Leu Gly Val Gly Lys Gln Tyr Tyr Gly Leu
305 310 315 320
Ala Leu Leu Gly Leu Ile Ile Pro Gln Val Ile Phe Gln Phe Gln Tyr
325 330 335
Phe Leu Lys Asp Pro Ile Lys Tyr Asp Val Lys Tyr Gln Ala Ser Ala
340 345 350
Gln Pro Phe Leu Val Leu Gly Ile Leu Val Thr Ala Leu Ala Thr Ser
355 360 365
His
<210> 6
<211> 1224
<212> DNA
<213> 人工序列
<400> 6
atggattcct tgttgttgtt gggttctgtt tctaagccat gttggagatt gtctttctct 60
gcttctgcta aattgtctac tgctactaga ggttaccatg ttcctattag attcgctaac 120
tcttccgctt ggtccactca agaaagaaga tacttcggtc aattgcaagg tcatttgatt 180
aatcatcata tcaccattga tgctgaaaaa tcttcttttt acagaagggc tgataagaag 240
ggtttagtta acgctacttc tgaacctcca tttgcttctg aaccagaatc atataaccca 300
aataactttt ggagatctat gcaatcagct actgatgcct tctatagatt ttctagacca 360
cacactgtta ttggtactgc tttgtctatt ttgtctgtct ctttattagc aattgaaaga 420
ttatctgatc tatcaccatt gttcttcact ggtttgctag aagctatcgt cgctgccttg 480
tttatgaata tctacatcgt tggtttgaac caattattcg acgttgaaat cgataaagtt 540
aataagccat acttgccatt agctagtggt gaatattcca ttggtactgg tattttgatc 600
gttgctgctt ttgctgttat gagtttctgg ttgggttggt ttgttggttc aggtccttta 660
ctttgggctt tatccatctc ttttatcttg ggtactgctt attctattaa tttgccattg 720
ttaagatgga aaagatttgc cttagttgct gctatgtgta tcttagttgt tagagctgtt 780
attgttcaat tagctttctt tttgcatatt caaactttcg tttaccgtag accagctatt 840
ttaactagac cattaatttt cgctactgcc ttcatgtcat tcttctctgt cgttattgct 900
ttgtttaaag atattccaga tattgaaggt gacgctattt tcgggattag atctttcact 960
gttagattgg gtcaaaagag agttttctgg atctgtgtct acctattgga aatggcttac 1020
ggtgttgctg ttttagtcgg tgcagcttct ccatctccat ggtctaagtt ggttaccgtt 1080
ttaggtcatg ttgttttggc ttccatttta tggttgaatg ctaagtccgt tgatttgact 1140
aacaaaactg ctattacttc tttctacatg ttcatttgga agttgttcta cgctgaatat 1200
ttgttgattc cattggttag ataa 1224
<210> 7
<211> 1194
<212> DNA
<213> 人工序列
<400> 7
atggtatcat ccttcagctt tccttctttt gcagttacca agtacacccc tcaacaaggt 60
tttttactac gtaaattgag accattcagt agtcaacgta gagatgctga tattgctttg 120
ttgtttaaag ttcaaaccga aaataagatt ttcagtgcgc taaaaagttc agatccacaa 180
agtagttaca atttggataa gccattgtta aggcatactt ctagtatcag aaagctgtct 240
ccacctgcag ccactacgtc tgaacatgaa aatgtacctt tgagtagctt gtctaaagcc 300
attgacattt tttttagatt tataagaccc tatgcgatag tatgcacaat gtttggaata 360
atgagcgtta gcttattacc agttgaaacc ctggctgact taacaccgaa attttttctt 420
ggattaggta aggccatgat tgcagtggtc tcaatgaact tattctctgt cagtgttaac 480
caattttatg acgttgaatt agataaagta aacaaacctt atttgccctt agcatccggt 540
gagttgtcaa tggaagcggg tgctgcattt gttatcttgg cttcttcaat gggtatcagc 600
tttggtttga tgctacaatc accaccttta ttgtgtacga ttttaacatt ctttctattc 660
ggaggagctt atagtattga tttaccgttc ttgagatgga aaaaacatcc tgttttggcc 720
gtagtatgca ttactgcgat gagaggttta gctctgcagc tgggggtctt cttccatatc 780
caaaaatatg tattaggaaa gcctatggct ctaactcgta gtgtggtgtt cgtcaccatt 840
ttcatgtgtg tcttcaacat cgctatttca ttaattaaag atttaccgga tgttgatggt 900
gacaaggcac acggcttcca gaatatgacc attagattcg gaaaagaaaa agtgttttgg 960
gggtgcacct ctttaatgtt agccacatat ggtgctgcag tggcaatggg tttctcctct 1020
ccttttcttg ctactaaact tataactgtg atagcccata gcgcactagg gctatttgtg 1080
ttacttagag cgagaagcat aaaactagac gacgacgaat caacacaatc ttactactta 1140
cttttgtggg atctgtgcaa gattgaatac ttgttagcac catttgttag ataa 1194
<210> 8
<211> 1176
<212> DNA
<213> 人工序列
<400> 8
atggttagta gatgtgcttc tccatctttt tctattacta aatatactcc acatcaaggt 60
agtttattaa cttctttaaa accttttagt tctcaaaaac caggtgctag aattgaatat 120
aaattacaac aaaatcatat attttgtgct ttaagaaaag attctcatgc ttctttgact 180
catacacatg aaaatgaatt gttgtttaaa gataaatctc caactagaga aaaaggtaga 240
ttgtcagcta ctagttctga aaatgctcca tcatcttttt ctactaaatt agatatgttt 300
attaagtttg ttagaccata tgctactatt ggaattattg gtaatactat ttgtatgtgt 360
attttaccag ttcaaactat ggctgatttg tctcctagat tctttattgg tgttgctcaa 420
gctattgcat ctatggtttt gatgaatttg tttaatgttg ctgttaatca agtttatgat 480
gttgaattag ataaagtaaa caaaccatat ttgcctttag cttcaggtgg tgtttctatg 540
acttctgcta ctttgtttac aattttaaca gctgctttat caattgcttt aggttatttt 600
tcttctccag cattatttta tggtagtata gctttctttt tatctgcttc agcttacagt 660
gttaattttc cattgttgag atggaaacat aatgctttag gtgcaattat ttctttaatg 720
ttatggggta tttcattgca aactggtgtt ttctttcata ttcaacaata tgttttaggt 780
aaaccaatgg ttttaaaaaa ttctttcata tatgcaatta tttttcaatc attgttttct 840
attgttgttg ctactttaaa ggatttgcca gatgttgaag gagatcaagc taatggttct 900
acaaacttaa caattttgat tggtaaagaa aaagttttct ggggttgtac ttcattgatg 960
ttggctacat atattggtac tgctgctttt ggtgctactt tacctatttt gaaaaataag 1020
ttggttacaa tggttgcaca ttctgcattg gcagtatttt tgtggttaca agctaaacaa 1080
atagatttgg ctgatgatgc ttctactcaa tcttattact tgttgatgtg gaaattgtgt 1140
aatattgaat atttgttgat tccattcgtt ggttaa 1176
<210> 9
<211> 1185
<212> DNA
<213> 人工序列
<400> 9
atggatttga gatccttgta ctctccatgt tctgctacat ctgttttgac tccacatcat 60
caaaaaattt tgactgctaa gccaactgtt caatcttcta aaatttcttt caagttctct 120
tcatcttctt cttccttaac tactattggt atttcccatt ctcataacat taagtctgcc 180
ccagtcaagc acactaagag attgtcaatt ttggcttgtt ctccaattga ctatgctgct 240
ggttctggtt ccggatctgg ttctgatcca ttattagtta aattgtcaga attccgtgac 300
gcttcctgga gattcttgag accacatact atcagaggta cagctttggg ttcttgtgct 360
ttggtggcta gggccttggt tgaaaacact cacttaatca gatggtcttt gttgttgaag 420
gctttgtctg gtgtttttgc tttaatttgt ggtaacggct acattgttgg tattaaccaa 480
atctatgaca ttggtattga taaggttaat aagccttatt tgccaattgc tgctggcgat 540
ttgtctgttc aatccgcttg gtacttggtc gttttcttcg ctgttgctgg tttgttgatt 600
gttagtttta actttggtac ttttattact tctttgtact gtttgggttt gtttttaggt 660
actgtttact ctgttcctcc attcagaatg aaaaagtatc cagttgctgc cttcttgatt 720
attgctaccg ttagaggttt cttgttgaac tttggtgttt accacgccac tagagctgct 780
ttgggtttga ctttcgaatg gtctagccct gttgctttca ttactacttt tgttactatg 840
ttcgctttgg ttatcgctat tactaaggac ttaccagatg ttgaaggaga tagaaagttt 900
caaatctcta ctttggctac caccttgggt gttagaaata ttgctttatt aggttcaggt 960
ttattattag ctaattactt gggtgctatt tttgctgctg tttacatgcc acaagctttt 1020
agatcttcat tgatgattcc agttcatgct attttattat tatctttgat ttttcaagcc 1080
tggatcttag aaagagctaa ttacactaaa gaagctattt tggctttcta tagattcatt 1140
tggaacttgt tctatgctga atacattgtt tttccattca tctaa 1185
<210> 10
<211> 1110
<212> DNA
<213> 人工序列
<400> 10
atggcaacat tgttgaatac attatcatta agttccgcta aattaactaa tagaagaaca 60
caatctcatc aaccatcttc atttttcttt ttaccagttt ctactccttc ttttactaga 120
agaattttag ttgttagagc tgctgaaact gatactaatg aagtaaaacc atcttctggt 180
tcatctatta atcaattgtt aggtattaag ggtgcttcac aagaaactaa taagtggaaa 240
attagattgc aattgatgaa accagttact tggccaccat tagtttgggg tgttgtttgt 300
ggtgctgctg catctggtaa ttttcattgg aatgttgaag atgtaggtaa atctattttg 360
tgtatgataa tgtctggtcc atgtttaact ggttatactc aaactttgaa tgattggtat 420
gatagagaaa ttgatgctat taatgaacca tatagaccaa ttccatcagg agctgtttct 480
gaaaatgaag tgactactca aatttgggtt ttgttgttag gtggtttagg tttagcaggt 540
ttattagatg ttttagctgg tcataatttt cctattgtat tttatctagc tttaggtggt 600
tctttattat catatatata ttctgctcct ccattgaaat tgaaacaatt tggttgggtt 660
ggtaattttg cattgggtgc ttcttatatt tctttaccat ggtgggctgg tcaagcttta 720
tttggtacat taactcctga tgttattgtt ttgactttat tatattctat tgcaggttta 780
ggtattgcta ttattaatga ttttaaatct attgaaggcg atagagcttt gggtttgcaa 840
tctttaccag ttgcatttgg tgttgataca gctaagtgga tttgtgtagg tgctattgat 900
atcactcaat tgtctattgc tggttatcta ttaggtgttg gtaaacaata ttatggtttg 960
gcattgttag gtttgattat tccacaagtg atttttcaat ttcaatattt cttaaaagat 1020
ccaattaagt atgatgttaa atatcaagct tctgctcaac catttttagt tttaggtatt 1080
ttagttacag ctttagctac ttctcattaa 1110
<210> 11
<211> 1224
<212> DNA
<213> Epimedium koreanum Nakai
<400> 11
atggattctc tactccttct tgggtctgta tcgaaacctt gttggcgtct ttcgttttca 60
gcttctgcca agctatcaac tgctacaagg ggttatcatg taccaattag atttgcaaac 120
tcatcagcat ggtctactca agaaagacgc tactttggac agttacaggg acatcttatt 180
aatcatcaca tcacaattga tgcagaaaaa tcttcatttt ataggagggc cgacaagaag 240
gggttagtga atgctacttc agaaccacct tttgcatcgg agcctgaatc ttataatcca 300
aacaactttt ggagatctat gcaaagcgcc acagatgcct tttatcggtt ttcacggccc 360
catactgtca taggcacagc attaagtata ctctcagtat cattacttgc tattgagagg 420
ttatcagatc tttctccatt gttcttcact gggttgctgg aggcaattgt tgcggctctg 480
ttcatgaata tttacatagt cgggttaaat caactctttg acgtagaaat agataaggtt 540
aacaagccct atcttcctct tgcatctgga gaatactcca ttggaacggg catcctgatc 600
gttgcagctt ttgccgtgat gagcttttgg ctaggatggt ttgttggttc tgggccatta 660
ttatgggcac tttccattag ctttattctt gggactgcat attcaattaa tttaccatta 720
ttgagatgga agcgatttgc tttagttgct gcaatgtgta tcctggttgt ccgagcggtg 780
attgttcaac ttgcgttttt tctgcacata cagacatttg tttatagaag accagccatc 840
ttgacgaggc cattgatatt tgcaactgca ttcatgagct tcttctcagt tgttatagct 900
ctattcaagg atatacctga tattgaggga gacgcgattt ttggcatccg ttcttttact 960
gtccgccttg ggcaaaagcg ggtattctgg atttgtgtat accttcttga aatggcttat 1020
ggtgtcgccg tattggttgg agctgcttct ccctcccctt ggagcaaact tgttacggtt 1080
ttaggtcatg tagtcttggc ttcaatcctg tggctcaatg ctaaatccgt ggacctgaca 1140
aacaaaactg caataacatc cttttatatg tttatttgga agctctttta tgcagagtat 1200
ttgctcatcc cattggtcag atga 1224
<210> 12
<211> 1194
<212> DNA
<213> Epimedium koreanum Nakai
<400> 12
atggtttcaa gcttttcttt tccatctttt gcagtcacca aatacactcc tcaacaaggt 60
tttcttttga gaaagctgag accttttagt tcccaaagga gagatgcaga tattgctcta 120
ctgttcaagg tccaaacaga gaataaaatc ttcagtgctt tgaagagtag tgatccacaa 180
agctcttata atcttgataa accactcttg aggcacacaa gttcaattag gaaactctct 240
ccaccagctg ctactacatc agagcatgaa aatgtaccat taagtagtct ttccaaggca 300
atagatatat ttttcaggtt tattcgcccg tatgcaattg tttgcacgat gttcggcata 360
atgtctgttt cccttcttcc agtagaaaca ttggctgatc taactccaaa atttttcctc 420
ggtctaggga aggcaatgat agcagtggtg tctatgaatc tctttagtgt gtccgtaaat 480
caattttacg atgttgagct tgataaggtt aacaagccat atctccccct tgcttcagga 540
gaactttcta tggaggctgg ggcagccttt gttatcttgg caagttccat gggaatttct 600
tttgggttga tgcttcagtc tccaccgttg ttatgtacaa ttctgacatt cttcctcttt 660
ggtggtgctt attcaattga tcttcccttc ctgagatgga agaaacatcc agtcctagct 720
gtggtatgta tcactgccat gagagggctt gctttacaac taggtgtatt ttttcacatt 780
cagaaatatg tgcttgggaa gcctatggcc ttgacaagat cagtagtctt tgtaacgatt 840
ttcatgtgtg tcttcaacat tgccatttca ttaatcaagg atttacctga tgtggatgga 900
gacaaagctc atggcttcca aaacatgact atacgcttcg gtaaagaaaa ggtattttgg 960
ggttgcactt ccctcatgtt ggcaacttat ggcgctgcag tggcaatggg gttctcttcg 1020
ccattcctgg caactaagct aatcactgta attgcacata gtgcacttgg tttgtttgtc 1080
ttgcttcgtg ctcgatcaat taaacttgat gatgatgaat caacacagtc atattaccta 1140
cttctatggg atctttgtaa aattgagtac ttgcttgccc cattcgttcg ttga 1194
<210> 13
<211> 1176
<212> DNA
<213> Epimedium koreanum Nakai
<400> 13
atggtttcta gatgtgcttc tccgtctttc tccatcacca aatacactcc tcatcaaggt 60
tcacttttaa caagtctaaa acccttcagt tcccaaaaac caggagctag aatagaatat 120
aaattgcaac aaaatcatat attttgtgct ctgagaaaag attcacatgc atccctcaca 180
catactcatg aaaatgagct gctcttcaaa gacaagagcc caaccagaga aaaaggacgc 240
ctttctgcaa caagttctga aaacgcaccc tcaagttttt ccactaaatt agatatgttt 300
atcaagtttg ttcgtcccta tgcaaccatc ggcattattg ggaatacaat atgcatgtgc 360
atacttccag tgcaaacaat ggctgatctg tctccaaggt tttttattgg tgtagctcag 420
gcaatagcaa gcatggtgct tatgaatcta tttaatgttg ccgtgaatca agtatatgac 480
gttgagctcg ataaggtaaa caagccatat ttacctcttg cttctggagg agtctctatg 540
acaagtgcta ctctatttac aatcttgaca gccgctctga gcattgcatt gggatacttt 600
tcatctccag cactgtttta cggatctatt gctttctttc tctctgcctc cgcatactct 660
gtcaatttcc ccttattgag atggaaacac aatgcactgg gtgccattat aagtctcatg 720
ctttggggga tttcactaca aactggtgtc ttcttccaca ttcagcaata cgtgcttgga 780
aagcccatgg ttttaaaaaa ttcgttcatc tatgcaataa ttttccagtc cctattcagc 840
attgtcgtcg caacactcaa ggatttacct gatgtcgaag gcgaccaagc taacggctct 900
accaacttga ctatactaat cggtaaagaa aaagtatttt ggggttgcac tagtctcatg 960
ttggcaacat atattggtac agcagccttt ggggcaactt taccgatcct gaagaacaag 1020
ctcgtcacta tggtagcgca cagtgcactt gctgtcttcc tttggcttca ggctaaacag 1080
attgatcttg cagatgatgc ctctacacaa tcttattact tgcttatgtg gaagctttgc 1140
aatatcgagt acttactcat tccattcgtt ggttaa 1176
<210> 14
<211> 1185
<212> DNA
<213> Epimedium koreanum Nakai
<400> 14
atggatctcc gctccttgta ttctccttgt tctgcaactt cagttcttac ccctcatcac 60
cagaagatac tcactgcaaa acccactgtc caatcctcca aaatttcctt taaattctcc 120
agcagttcct catcactgac caccattggc atttctcaca gccacaacat caaatccgcg 180
ccggtcaagc acacaaagcg tttatctatc ttggcttgta gtccaattga ctatgcggct 240
gggtctgggt ccgggtctgg gtctgacccg ttgttggtaa aattgtcaga attcagagat 300
gcatcctgga gatttctaag gcctcacacc attcgtggga cggcgttggg atcctgtgct 360
ttggtagcaa gagccttagt tgaaaacacg catctgataa gatggtcgtt gctgttgaag 420
gcattatccg gagtttttgc ccttatatgt ggcaatgggt atatagtggg gattaaccag 480
atctatgaca ttggaattga caaagtaaat aagccttatt tacctatagc tgcaggggat 540
ctttcagttc agtcagcatg gtatttggtg gtgttttttg cagttgctgg actattaatt 600
gtcagtttta actttggtac attcattaca tccctctact gtctcggtct cttcctcggc 660
accgtctatt ctgttcctcc attcaggatg aagaaatatc ctgttgcagc gtttctcatc 720
attgccactg ttcgtggatt tcttctaaat tttggagtct atcatgctac aagagctgca 780
ttaggactta catttgaatg gagttcacct gtggctttta tcacaacctt tgtgacaatg 840
tttgcactcg ttatagcaat aacaaaagac ctcccagatg tagagggaga ccgcaagttt 900
caaatatcga ccttggccac aacgcttggt gttagaaata ttgcattact tggttcaggg 960
cttctgctgg ctaattatct tggcgctata tttgcagcag tttacatgcc tcaggctttt 1020
agaagcagct tgatgatacc agttcatgca atcctactgt tgagtttgat attccaggca 1080
tggatattag aacgggccaa ttacaccaag gaagccatct tagcgttcta tcggtttatc 1140
tggaatctct tctatgcaga atatattgta ttccccttta tttaa 1185
<210> 15
<211> 1110
<212> DNA
<213> Epimedium koreanum Nakai
<400> 15
atggcaacct tgctaaacac tctctccttg tcttccgcaa aattaacaaa cagaagaacc 60
caatctcatc aaccttcttc tttctttttc ctaccggttt ccacaccatc cttcacccgg 120
agaatacttg tagtcagagc agctgaaact gatacaaatg aagttaaacc ctcaagtggt 180
tcgagcatca atcaacttct tggcattaaa ggagcttccc aagagacaaa caaatggaag 240
attcgtctcc aacttatgaa gcctgtgaca tggcctcctt tggtctgggg agtagtctgt 300
ggagctgctg cttctgggaa cttccactgg aatgtggaag atgttggaaa atcaattctc 360
tgtatgataa tgtctggacc atgtctcact ggctatacac aaacccttaa tgattggtat 420
gatcgagaaa ttgatgcaat aaatgagccc tatcgtccaa ttccttctgg ggcagtatct 480
gagaatgagg tgactacaca gatatgggtg ctgcttttag gtggccttgg cttggctggg 540
ttattagatg tattggcagg acataacttt cctatagttt tttaccttgc acttggtgga 600
tccttgcttt catacatata ttctgctccg ccattaaagc tcaaacagtt tggatgggtt 660
ggaaactttg ctcttggagc aagctacatt agcttgccat ggtgggctgg ccaagcttta 720
tttggaactc ttacacctga cgtaattgta cttacacttc tatatagcat agctgggctt 780
ggtatcgcca tcattaatga cttcaaaagt atcgaaggag atagggcact tggactgcag 840
tctcttccgg tggcttttgg cgttgatact gctaaatgga tatgcgttgg cgcaatagac 900
ataactcagc tttctattgc tggttatctt cttggggtgg gtaaacaata ttatggcttg 960
gccctattag gtttgataat tccgcaagtc atttttcagt ttcagtattt cctgaaggac 1020
ccaatcaagt atgatgtcaa atatcaggct agtgcacaac catttcttgt gcttggaata 1080
ttggtaacag ctctagcaac gagccactga 1110

Claims (10)

1.朝鲜淫羊藿来源的黄酮8-异戊烯基转移酶,其特征在于,氨基酸序列如SEQ ID NO.3所示。
2.编码权利要求1所述黄酮8-异戊烯基转移酶的基因。
3.携带权利要求2所述的基因的表达载体。
4.表达权利要求1所述8-异戊烯基转移酶的微生物细胞。
5.根据权利要求4所述的微生物细胞,其特征在于,在基因组上整合了SEQ ID NO.8所示的基因,或含有携带SEQ ID NO.8所示基因的重组质粒。
6.一种生产黄酮8-异戊烯基转移酶的方法,其特征在于,将权利要求4或5所述的微生物细胞接种至培养基中,于28~40℃培养至少12 h,收集黄酮8-异戊烯基转移酶。
7.根据权利要求6所述的方法,其特征在于,将表达权利要求1所述黄酮8-异戊烯基转移酶的大肠杆菌在培养基中,于35~40℃培养至OD600为0.04~0.06,加入终浓度为0.01~1 mM的IPTG,于28~30℃诱导表达至少8 h。
8.权利要求1所述的黄酮8-异戊烯基转移酶在催化山奈酚生产8-异戊烯基山奈酚,或在催化山奈酚生产含8-异戊烯基山奈酚的医用营养品或药物中的应用。
9.一种生产8-异戊烯基山奈酚的方法,其特征在于,将权利要求4或5所述的微生物细胞或其代谢产物接种至含山奈酚的培养基中,将山奈酚转化为8-异戊烯基山奈酚;所述代谢产物含黄酮8-异戊烯基转移酶。
10.权利要求1所述的黄酮8-异戊烯基转移酶,或权利要求4或5所述的微生物细胞在制备微生物细胞催化剂方面的应用。
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CN104894080A (zh) * 2015-05-14 2015-09-09 中国科学院华南植物园 一种类黄酮异戊烯基转移酶AhFDT3及其编码基因和应用
CN109207448A (zh) * 2017-06-30 2019-01-15 中国科学院上海生命科学研究院 新型黄酮异戊烯基转移酶及其应用

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CN104894080A (zh) * 2015-05-14 2015-09-09 中国科学院华南植物园 一种类黄酮异戊烯基转移酶AhFDT3及其编码基因和应用
CN109207448A (zh) * 2017-06-30 2019-01-15 中国科学院上海生命科学研究院 新型黄酮异戊烯基转移酶及其应用

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