CN108251461B - 一种制备右旋龙脑的方法 - Google Patents

一种制备右旋龙脑的方法 Download PDF

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CN108251461B
CN108251461B CN201810147374.4A CN201810147374A CN108251461B CN 108251461 B CN108251461 B CN 108251461B CN 201810147374 A CN201810147374 A CN 201810147374A CN 108251461 B CN108251461 B CN 108251461B
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谢新开
黄晓飞
杜好勉
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Suzhou Lead Biotechnology Co ltd
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Abstract

本发明提供一种以廉价易得的天然右旋樟脑为原料在酮还原酶的作用下制备右旋龙脑的方法。

Description

一种制备右旋龙脑的方法
技术领域
本发明属于生物制药和生物化工技术领域,具体涉及一种右旋龙脑的制备方法。
背景技术
右旋龙脑又叫做天然冰片,是一种重要的药材。右旋龙脑对于人们中枢神经的兴奋具有重要的调节功效,常被作为药引应用到各种中药的配方中,帮助中药提升其治疗效果。很多名贵的中成药都把它作为主要成分之一,如六神丸、健心片、牛黄上清丸等。右旋龙脑也是一种历史悠久的香料,常用于化妆品以及古龙水等。
目前,右旋龙脑都是从香樟、龙脑樟等植物中提取的,生产成本高,资源稀缺,市场缺口非常大。合成冰片(含有左旋龙脑,右旋龙脑以及异龙脑)一度得到广泛的应用,但是由于其中右旋龙脑的含量比较低(20%左右),其在药物和香料方面的应用价值无法跟天然冰片相比拟。因此探索一种温和、高效、经济的方法制备高纯度的右旋龙脑是非常有意义的。
右旋龙脑,其结构式如下所示:
Figure BDA0001579167520000011
工业制备右旋龙脑主要是从天然的右旋樟脑出发,还原制备右旋龙脑。主要是通过碱金属/NH3的方法(J.Org.Chem.,1979,44(4),594-599;J.Am.Chem.Soc.,1968,90(23),6486-6492;Tetrahedron Lett.;1987,28(29);3315-3318)。比如:Huffman等考察了各种碱金属在液氨中不对称还原樟脑,虽然选择性最高能做到85%,但是此类方法需要在-40℃以下的低温进行并且对环境不友好,因此很难得到工业化应用。其他一些还原方法也有一些报道(Tetrahedron Lett.;1981,22(3);179-180;现代有机合成方法与技术。北京:化学工业出版社.2003),比如连二亚硫酸钠作为还原剂、三异丙醇铝-异丙醇体系等。这些方法都存在转化率低,选择性差等缺点,无法进行产业化。
化学工作者还发展了一些其他制备右旋龙脑的方法。比如中国科学院广州化学研究所在1987年报道了(广州化工,1987,3,12-15),选用一种高旋光度的右旋松节油作原料合成右旋龙脑,虽然龙脑与异龙脑的比例高达94:6,比旋度在25以上,但是反应的收率只有20%左右,产业化价值不大。
发明内容
本发明针对现有技术的不足,提供了一种简单易行的合成右旋龙脑的新方法,该方法操作简单,条件温和,大幅度降低了生产的成本,适合大规模的工业化生产。
本发明公开了一种以廉价易得的天然右旋樟脑为原料在酮还原酶的作用下制备右旋龙脑的方法,反应流程如下:
Figure BDA0001579167520000031
具体包括如下步骤:取右旋樟脑置于缓冲溶液中,再向其中加入所述酮还原酶,得到混合溶液,使所述混合溶液在20-40℃下反应,得所述右旋龙脑。
优选地,所述酮还原酶的DNA序列具有与SEQ ID No.1、SEQ ID No.2和SEQ IDNo.3所示的任一序列90%以上相同。
更优选地,所述酮还原酶的DNA序列为SEQ ID No.1、SEQ ID No.2和SEQ ID No.3所示的任一序列。
优选地,所述酮还原酶的蛋白质序列具有与SEQ ID No.4、SEQ ID No.5和SEQ IDNo.6所示的任一序列90%以上的同源性。
更优选地,所述酮还原酶的蛋白质序列为SEQ ID No.4、SEQ ID No.5和SEQ IDNo.6所示的任一序列。
优选地,所述缓冲溶液为pH值为6.0-8.0,浓度为0.01-0.5mol/L的PBS缓冲溶液。
优选地,所述右旋樟脑和酮还原酶的重量比为20:1-50:1。
优选地,向所述缓冲溶液中加入右旋樟脑时,还加入葡萄糖、异丙醇、甲酸铵中的一种。
优选地,在所述混合溶液中,右旋樟脑与葡萄糖的摩尔比为1:(1.2-1.5);右旋樟脑与异丙醇的摩尔比为1:(5-10);右旋樟脑与甲酸铵的摩尔比为1:(1.2-1.5)。
优选地,向所述缓冲溶液中加入所述酮还原酶后,还加入葡萄糖脱氢酶、甲酸脱氢酶、NAD+、NADP+中的一种或多种。
优选地,所述葡萄糖脱氢酶采购自苏州引航生物科技有限公司,商品编号YH1901,所述甲酸脱氢酶采购自苏州引航生物科技有限公司,商品编号YH1805。
具体实施方式
本发明旨在提供一种生物催化制备右旋龙脑的方法,所述右旋龙脑结构式如下:
Figure BDA0001579167520000041
下面结合具体实施例对本发明做进一步详细的说明,但本发明并不限于以下实施例。
实施例1:
右旋樟脑2.5g、葡萄糖3.6g置于100mL的三口烧瓶,加入50mL pH=6.5,0.05M的PBS缓冲液。将三口烧瓶放入反应锅中,设置转速850rpm,温度30℃。然后分别加入5mg NADP+,100mg葡萄糖脱氢酶(采购自苏州引航生物科技有限公司:商品编号YH1901)、以及100mg酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2022)。开始反应,反应过程中用2M的NaOH溶液将pH维持在6.5左右,HPLC监测。24小时后反应转化率>99%,右旋龙脑:异龙脑97:3。
实施例2:
右旋樟脑2.5g、葡萄糖3.6g置于100mL的三口烧瓶,加入50mL pH=6.5,0.05M的PBS缓冲液。将三口烧瓶放入反应锅中,设置转速850rpm,温度30℃。然后分别加入5mg NADP+,100mg葡萄糖脱氢酶(采购自苏州引航生物科技有限公司:商品编号YH1901)、以及100mg酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2067)。开始反应,反应过程中用2M的NaOH溶液将pH维持在6.5左右,HPLC监测。24小时后反应转化率98%,右旋龙脑:异龙脑>99.5:0.5。
实施例3:
右旋樟脑2.5g、葡萄糖3.6g置于100mL的三口烧瓶,加入50mL pH=6.5,0.05M的PBS缓冲液。将三口烧瓶放入反应锅中,设置转速850rpm,温度30℃。然后分别加入5mg NADP+,100mg葡萄糖脱氢酶(采购自苏州引航生物科技有限公司:商品编号YH1901)、以及100mg酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2069)。开始反应,反应过程中用2M的NaOH溶液将pH维持在6.5左右,HPLC监测。24小时后反应转化率95%,右旋龙脑:异龙脑96:4。
实施例4:
右旋樟脑2.5g、异丙醇10mL加至装有80mL pH=6.5,0.1M PBS缓冲液的250mL反应器中搅拌均匀。依次加入酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2067)100mg,NADP+5mg。在30℃搅拌24h,HPLC监测反应转化率>99.5%,右旋龙脑:异龙脑>99.8:0.2。
实施例5:
右旋樟脑2.5g、甲酸铵2g加至装有100mL pH=6.5,0.1M PBS缓冲液的250mL反应器中搅拌均匀。依次加入NADP+5mg,酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2067)100mg,甲酸脱氢酶100mg(采购自苏州引航生物科技有限公司:商品编号YH1805)。开始反应,在30℃搅拌24h,HPLC监测反应转化率>98%,右旋龙脑:异龙脑>97:3。
实施例6:
右旋樟脑25g、异丙醇100mL加至装有800mL pH=6.5,0.1M PBS缓冲液的2000mL反应器中搅拌均匀。依次加入酮还原酶粉(采购自苏州引航生物科技有限公司:商品编号YH2067)1g,NADP+50mg。在30℃搅拌24h,HPLC监测反应转化率>99.5%,右旋龙脑:异龙脑>99.8:0.2。反应完毕,反应体系用二氯甲烷萃取,合并有机相,干燥,脱溶,得到右旋龙脑粗品24.8克。
上述实施例中,所使用的酮还原酶YH2022、YH2067、YH2069分别具有SEQ ID No.1、SEQ ID No.2和SEQ ID No.3所示的DNA序列和SEQ ID No.4、SEQ ID No.5和SEQ ID No.6所示的蛋白质序列:
SEQ ID No.1:
ATGGTTAAGCAAGAATTCTTTAAGCTGAACAATGGCCATGAGATGCCCGGTGTGGCCATCGTTGGTACCGGTACCAAGTGGCACAAGGTTAATGAGACAGATGAGAACTTCTCACAGACACTGGTAGATCAATTGAAATACGCTCTGTCTCTGCCAGGTGTTGTTCATCTGGATGCCGCTGAATTTTATATGACCTATAGAGAGGTCGGACGTGCACTAGCTGAGACTTCGAAGCCCCGTGATGAGATATTCATCACTGATAAATACTGGACTTTGAGCAAAGTTACTGAGAATCCCATTGTAGGTTTAGAGACTGGGTTGAAAAGACTCGGATTAGAGTACGTAGACTTGTACCTGTTGCATAGTCCCTTTATCTCTAAGGAAACCAACGGGTTCTCATTAGAGGAGGCCTGGGGTATGATGGAGGAATTATATCACAGTGGTAAAGCCAAGAATATTGGCGTCTCCAACTTTGCTAAGGAGGACTTAGAGAGAGTTTTGAAGGTCTGCAAAGTCAAGCCACAGGTCAATCAAATTGAGTTTAATGCCTTCTTACAAAACCAAACTCCTGGTATCTACAACTTTTGCAAGCAAAATGACATTCAATTAGCTGCATATTCTCCTCTAGGTCCTTTACAGAAAAAGCCAGCCGACGGTAATTCACAACCATTTTATAGCTATATCAACAAGCTGGCACAGCACTACAACAAAACCCCCGGTCAGGTTTTGTTGAGATGGGTTACCAAGCGTGGTGTCGTTGCTGTTACCACTTCTGAGAAGAAGGAGAGAATTAAACAAGCTCAGGAGATATTTGAATTTGATTTGAAAGATGATGAAGTTACTGAAATTACTAAACTAGGTCTAGACCACGAGCCTTTGAGACTGTATTGGCATGATCAATACAATAAGTACAACTCAGAGTCCCAGAAGGCCTAA
SEQ ID No.2:
ATGTCTAACGGTAAAACCTTCACCCTGTCTAACGGTGTTAAAATCCCGGGTGTTGGTTTCGGTACCTTCGCTTCTGAAGGTTCTAAAGGTGAAACCTACACCGCTGTTACCACCGCTCTGAAAACCGGTTACCGTCACCTGGACTGCGCTTGGTACTACCTGAACGAAGGTGAAGTTGGTGAAGGTATCCGTGACTTCCTGAAAGAAAACCCGTCTGTTAAACGTGAAGACATCTTCGTTTGCACCAAAGTTTGGAACCACCTGCACCGTTACGAAGACGTTCTGTGGTCTATCGACGACTCTCTGAAACGTCTGGGTCTGGACTACGTTGACATGTTCCTGGTTCACTGGCCGATCGCTGCTGAAAAAAACGGTCAGGGTGAACCGAAAATCGGTCCGGACGGTAAATACGTTATCCTGAAAGACCTGACCGAAAACCCGGAACCGACCTGGCGTGCTATGGAAAAAATCTACGAAGACCGTAAAGCTCGTTCTATCGGTGTTTCTAACTGGACCATCGCTGACCTGGAAAAAATGTCTAAATTCGCTAAAGTTATGCCGCACGCTAACCAGATCGAAATCCACCCGTTCCTGCCGAACGAAGAACTGGTTCAGTACTGCTTCTCTAAAAACATCATGCCGGTTGCTTACTCTCCGCTGGGTTCTCAGAACCAGGTTCCGACCACCGGTGAACGTGTTTCTGAAAACAAAACCCTGAACGAAATCGCTGAAAAAGGTGGTAACACCCTGGCTCAGGTTCTGATCGCTTGGGGTCTGCGTCGTGGTTACGTTGTTCTGCCGAAATCTTCTAACCCGAAACGTATCGAATCTAACTTCAAATCTATCGAACTGTCTGACGCTGACTTCGAAGCTATCAACGCTGTTGCTAAAGGTCGTCACTTCCGTTTCGTTAACATGAAAGACACCTTCGGTTACGACGTTTGGCCGGAAGAAACCGCTAAAAACCTGTCTGCTTAA
SEQ ID No.3:
ATGACCAACCGcCTGCAGGGTAAAGTCGCACTGGTTACCGGTGGTGCTTCCGGTGTGGGCCTGGAAGTAGTGAAACTGCTCCTGGGTGAAGGCGCGAAAGTAGCGTTCAGCGACATCAACGAAGCAGCAGGGCAGCAGTTAGCAGCTGAGCTGGGCGAACGTAGTATGTTCGTGCGTCATGATGTCAGCAGCGAGGCAGATTGGACCCTGGTTATGGCAGCAGTACAGCGTCGCCTGGGTACCCTGAACGTGCTGGTGAACAACGCGGGTATTCTGCTGCCGGGCGACATGGAGACCGGTCGCCTGGAGGATTTTTCGCGCCTGCTGAAAATCAACACCGAAAGCGTGTTCATCGGTTGCCAGCAGGGCATTGCGGCCATGAAAGAAACTGGTGGTTCAATCATCAACATGGCTTCTGTTTCGTCTTGGCTGCCAATCGAACAATATGCAGGCTACAGCGCCTCAAAAGCAGCTGTCAGCGCCCTGACTCGCGCCGCAGCGCTTTCGTGTCGTAAACAAGGTTACGCTATCCGTGTTAACTCGATCCACCCGGATGGTATCTACACCCCGATGATGCAGGCGTCCCTGCCAAAAGGCGTGTCTAAGGAAATGGTGTTGCACGACCCAAAGCTGAACCGCGCGGGTCGTGCTTACATGCCGGAACGTATCGCGCAGCTGGTTCTGTTCCTTGCAAGCGACGAATCCAGCGTGATGTCCGGGAGTGAGCTGCACGCGGATAACAGCATTCTGGGTATGGGGCTGTAA
SEQ ID No.4:
MVKQEFFKLNNGHEMPGVAIVGTGTKWHKVNETDENFSQTLVDQLKYALSLPGVVHLDAAEFYMTYREVGRALAETSKPRDEIFITDKYWTLSKVTENPIVGLETGLKRLGLEYVDLYLLHSPFISKETNGFSLEEAWGMMEELYHSGKAKNIGVSNFAKEDLERVLKVCKVKPQVNQIEFNAFLQNQTPGIYNFCKQNDIQLAAYSPLGPLQKKPADGNSQPFYSYINKLAQHYNKTPGQVLLRWVTKRGVVAVTTSEKKERIKQAQEIFEFDLKDDEVTEITKLGLDHEPLRLYWHDQYNKYNSESQKA*
SEQ ID No.5:
MSNGKTFTLSNGVKIPGVGFGTFASEGSKGETYTAVTTALKTGYRHLDCAWYYLNEGEVGEGIRDFLKENPSVKREDIFVCTKVWNHLHRYEDVLWSIDDSLKRLGLDYVDMFLVHWPIAAEKNGQGEPKIGPDGKYVILKDLTENPEPTWRAMEKIYEDRKARSIGVSNWTIADLEKMSKFAKVMPHANQIEIHPFLPNEELVQYCFSKNIMPVAYSPLGSQNQVPTTGERVSENKTLNEIAEKGGNTLAQVLIAWGLRRGYVVLPKSSNPKRIESNFKSIELSDADFEAINAVAKGRHFRFVNMKDTFGYDVWPEETAKNLSA*
SEQ ID No.6:
MTNRLQGKVALVTGGASGVGLEVVKLLLGEGAKVAFSDINEAAGQQLAAELGERSMFVRHDVSSEADWTLVMAAVQRRLGTLNVLVNNAGILLPGDMETGRLEDFSRLLKINTESVFIGCQQGIAAMKETGGSIINMASVSSWLPIEQYAGYSASKAAVSALTRAAALSCRKQGYAIRVNSIHPDGIYTPMMQASLPKGVSKEMVLHDPKLNRAGRAYMPERIAQLVLFLASDESSVMSGSELHADNSILGMGL*
上述实施例只为说明本发明的技术构思及特点,其目的在于让熟悉此项技术的人士能够了解本发明的内容并据以实施,并不能以此限制本发明的保护范围。凡根据本发明精神实质所作的等效变化或修饰,都应涵盖在本发明的保护范围之内。
序列表
<110> 苏州引航生物科技有限公司
<120> 一种制备右旋龙脑的方法
<130> 2018
<160> 6
<170> SIPOSequenceListing 1.0
<210> 1
<211> 936
<212> DNA
<213> 人工序列(未知)
<400> 1
atggttaagc aagaattctt taagctgaac aatggccatg agatgcccgg tgtggccatc 60
gttggtaccg gtaccaagtg gcacaaggtt aatgagacag atgagaactt ctcacagaca 120
ctggtagatc aattgaaata cgctctgtct ctgccaggtg ttgttcatct ggatgccgct 180
gaattttata tgacctatag agaggtcgga cgtgcactag ctgagacttc gaagccccgt 240
gatgagatat tcatcactga taaatactgg actttgagca aagttactga gaatcccatt 300
gtaggtttag agactgggtt gaaaagactc ggattagagt acgtagactt gtacctgttg 360
catagtccct ttatctctaa ggaaaccaac gggttctcat tagaggaggc ctggggtatg 420
atggaggaat tatatcacag tggtaaagcc aagaatattg gcgtctccaa ctttgctaag 480
gaggacttag agagagtttt gaaggtctgc aaagtcaagc cacaggtcaa tcaaattgag 540
tttaatgcct tcttacaaaa ccaaactcct ggtatctaca acttttgcaa gcaaaatgac 600
attcaattag ctgcatattc tcctctaggt cctttacaga aaaagccagc cgacggtaat 660
tcacaaccat tttatagcta tatcaacaag ctggcacagc actacaacaa aacccccggt 720
caggttttgt tgagatgggt taccaagcgt ggtgtcgttg ctgttaccac ttctgagaag 780
aaggagagaa ttaaacaagc tcaggagata tttgaatttg atttgaaaga tgatgaagtt 840
actgaaatta ctaaactagg tctagaccac gagcctttga gactgtattg gcatgatcaa 900
tacaataagt acaactcaga gtcccagaag gcctaa 936
<210> 2
<211> 978
<212> DNA
<213> 人工序列(未知)
<400> 2
atgtctaacg gtaaaacctt caccctgtct aacggtgtta aaatcccggg tgttggtttc 60
ggtaccttcg cttctgaagg ttctaaaggt gaaacctaca ccgctgttac caccgctctg 120
aaaaccggtt accgtcacct ggactgcgct tggtactacc tgaacgaagg tgaagttggt 180
gaaggtatcc gtgacttcct gaaagaaaac ccgtctgtta aacgtgaaga catcttcgtt 240
tgcaccaaag tttggaacca cctgcaccgt tacgaagacg ttctgtggtc tatcgacgac 300
tctctgaaac gtctgggtct ggactacgtt gacatgttcc tggttcactg gccgatcgct 360
gctgaaaaaa acggtcaggg tgaaccgaaa atcggtccgg acggtaaata cgttatcctg 420
aaagacctga ccgaaaaccc ggaaccgacc tggcgtgcta tggaaaaaat ctacgaagac 480
cgtaaagctc gttctatcgg tgtttctaac tggaccatcg ctgacctgga aaaaatgtct 540
aaattcgcta aagttatgcc gcacgctaac cagatcgaaa tccacccgtt cctgccgaac 600
gaagaactgg ttcagtactg cttctctaaa aacatcatgc cggttgctta ctctccgctg 660
ggttctcaga accaggttcc gaccaccggt gaacgtgttt ctgaaaacaa aaccctgaac 720
gaaatcgctg aaaaaggtgg taacaccctg gctcaggttc tgatcgcttg gggtctgcgt 780
cgtggttacg ttgttctgcc gaaatcttct aacccgaaac gtatcgaatc taacttcaaa 840
tctatcgaac tgtctgacgc tgacttcgaa gctatcaacg ctgttgctaa aggtcgtcac 900
ttccgtttcg ttaacatgaa agacaccttc ggttacgacg tttggccgga agaaaccgct 960
aaaaacctgt ctgcttaa 978
<210> 3
<211> 765
<212> DNA
<213> 人工序列(未知)
<400> 3
atgaccaacc gcctgcaggg taaagtcgca ctggttaccg gtggtgcttc cggtgtgggc 60
ctggaagtag tgaaactgct cctgggtgaa ggcgcgaaag tagcgttcag cgacatcaac 120
gaagcagcag ggcagcagtt agcagctgag ctgggcgaac gtagtatgtt cgtgcgtcat 180
gatgtcagca gcgaggcaga ttggaccctg gttatggcag cagtacagcg tcgcctgggt 240
accctgaacg tgctggtgaa caacgcgggt attctgctgc cgggcgacat ggagaccggt 300
cgcctggagg atttttcgcg cctgctgaaa atcaacaccg aaagcgtgtt catcggttgc 360
cagcagggca ttgcggccat gaaagaaact ggtggttcaa tcatcaacat ggcttctgtt 420
tcgtcttggc tgccaatcga acaatatgca ggctacagcg cctcaaaagc agctgtcagc 480
gccctgactc gcgccgcagc gctttcgtgt cgtaaacaag gttacgctat ccgtgttaac 540
tcgatccacc cggatggtat ctacaccccg atgatgcagg cgtccctgcc aaaaggcgtg 600
tctaaggaaa tggtgttgca cgacccaaag ctgaaccgcg cgggtcgtgc ttacatgccg 660
gaacgtatcg cgcagctggt tctgttcctt gcaagcgacg aatccagcgt gatgtccggg 720
agtgagctgc acgcggataa cagcattctg ggtatggggc tgtaa 765
<210> 4
<211> 311
<212> PRT
<213> 人工序列(未知)
<400> 4
Met Val Lys Gln Glu Phe Phe Lys Leu Asn Asn Gly His Glu Met Pro
1 5 10 15
Gly Val Ala Ile Val Gly Thr Gly Thr Lys Trp His Lys Val Asn Glu
20 25 30
Thr Asp Glu Asn Phe Ser Gln Thr Leu Val Asp Gln Leu Lys Tyr Ala
35 40 45
Leu Ser Leu Pro Gly Val Val His Leu Asp Ala Ala Glu Phe Tyr Met
50 55 60
Thr Tyr Arg Glu Val Gly Arg Ala Leu Ala Glu Thr Ser Lys Pro Arg
65 70 75 80
Asp Glu Ile Phe Ile Thr Asp Lys Tyr Trp Thr Leu Ser Lys Val Thr
85 90 95
Glu Asn Pro Ile Val Gly Leu Glu Thr Gly Leu Lys Arg Leu Gly Leu
100 105 110
Glu Tyr Val Asp Leu Tyr Leu Leu His Ser Pro Phe Ile Ser Lys Glu
115 120 125
Thr Asn Gly Phe Ser Leu Glu Glu Ala Trp Gly Met Met Glu Glu Leu
130 135 140
Tyr His Ser Gly Lys Ala Lys Asn Ile Gly Val Ser Asn Phe Ala Lys
145 150 155 160
Glu Asp Leu Glu Arg Val Leu Lys Val Cys Lys Val Lys Pro Gln Val
165 170 175
Asn Gln Ile Glu Phe Asn Ala Phe Leu Gln Asn Gln Thr Pro Gly Ile
180 185 190
Tyr Asn Phe Cys Lys Gln Asn Asp Ile Gln Leu Ala Ala Tyr Ser Pro
195 200 205
Leu Gly Pro Leu Gln Lys Lys Pro Ala Asp Gly Asn Ser Gln Pro Phe
210 215 220
Tyr Ser Tyr Ile Asn Lys Leu Ala Gln His Tyr Asn Lys Thr Pro Gly
225 230 235 240
Gln Val Leu Leu Arg Trp Val Thr Lys Arg Gly Val Val Ala Val Thr
245 250 255
Thr Ser Glu Lys Lys Glu Arg Ile Lys Gln Ala Gln Glu Ile Phe Glu
260 265 270
Phe Asp Leu Lys Asp Asp Glu Val Thr Glu Ile Thr Lys Leu Gly Leu
275 280 285
Asp His Glu Pro Leu Arg Leu Tyr Trp His Asp Gln Tyr Asn Lys Tyr
290 295 300
Asn Ser Glu Ser Gln Lys Ala
305 310
<210> 5
<211> 325
<212> PRT
<213> 人工序列(未知)
<400> 5
Met Ser Asn Gly Lys Thr Phe Thr Leu Ser Asn Gly Val Lys Ile Pro
1 5 10 15
Gly Val Gly Phe Gly Thr Phe Ala Ser Glu Gly Ser Lys Gly Glu Thr
20 25 30
Tyr Thr Ala Val Thr Thr Ala Leu Lys Thr Gly Tyr Arg His Leu Asp
35 40 45
Cys Ala Trp Tyr Tyr Leu Asn Glu Gly Glu Val Gly Glu Gly Ile Arg
50 55 60
Asp Phe Leu Lys Glu Asn Pro Ser Val Lys Arg Glu Asp Ile Phe Val
65 70 75 80
Cys Thr Lys Val Trp Asn His Leu His Arg Tyr Glu Asp Val Leu Trp
85 90 95
Ser Ile Asp Asp Ser Leu Lys Arg Leu Gly Leu Asp Tyr Val Asp Met
100 105 110
Phe Leu Val His Trp Pro Ile Ala Ala Glu Lys Asn Gly Gln Gly Glu
115 120 125
Pro Lys Ile Gly Pro Asp Gly Lys Tyr Val Ile Leu Lys Asp Leu Thr
130 135 140
Glu Asn Pro Glu Pro Thr Trp Arg Ala Met Glu Lys Ile Tyr Glu Asp
145 150 155 160
Arg Lys Ala Arg Ser Ile Gly Val Ser Asn Trp Thr Ile Ala Asp Leu
165 170 175
Glu Lys Met Ser Lys Phe Ala Lys Val Met Pro His Ala Asn Gln Ile
180 185 190
Glu Ile His Pro Phe Leu Pro Asn Glu Glu Leu Val Gln Tyr Cys Phe
195 200 205
Ser Lys Asn Ile Met Pro Val Ala Tyr Ser Pro Leu Gly Ser Gln Asn
210 215 220
Gln Val Pro Thr Thr Gly Glu Arg Val Ser Glu Asn Lys Thr Leu Asn
225 230 235 240
Glu Ile Ala Glu Lys Gly Gly Asn Thr Leu Ala Gln Val Leu Ile Ala
245 250 255
Trp Gly Leu Arg Arg Gly Tyr Val Val Leu Pro Lys Ser Ser Asn Pro
260 265 270
Lys Arg Ile Glu Ser Asn Phe Lys Ser Ile Glu Leu Ser Asp Ala Asp
275 280 285
Phe Glu Ala Ile Asn Ala Val Ala Lys Gly Arg His Phe Arg Phe Val
290 295 300
Asn Met Lys Asp Thr Phe Gly Tyr Asp Val Trp Pro Glu Glu Thr Ala
305 310 315 320
Lys Asn Leu Ser Ala
325
<210> 6
<211> 254
<212> PRT
<213> 人工序列(未知)
<400> 6
Met Thr Asn Arg Leu Gln Gly Lys Val Ala Leu Val Thr Gly Gly Ala
1 5 10 15
Ser Gly Val Gly Leu Glu Val Val Lys Leu Leu Leu Gly Glu Gly Ala
20 25 30
Lys Val Ala Phe Ser Asp Ile Asn Glu Ala Ala Gly Gln Gln Leu Ala
35 40 45
Ala Glu Leu Gly Glu Arg Ser Met Phe Val Arg His Asp Val Ser Ser
50 55 60
Glu Ala Asp Trp Thr Leu Val Met Ala Ala Val Gln Arg Arg Leu Gly
65 70 75 80
Thr Leu Asn Val Leu Val Asn Asn Ala Gly Ile Leu Leu Pro Gly Asp
85 90 95
Met Glu Thr Gly Arg Leu Glu Asp Phe Ser Arg Leu Leu Lys Ile Asn
100 105 110
Thr Glu Ser Val Phe Ile Gly Cys Gln Gln Gly Ile Ala Ala Met Lys
115 120 125
Glu Thr Gly Gly Ser Ile Ile Asn Met Ala Ser Val Ser Ser Trp Leu
130 135 140
Pro Ile Glu Gln Tyr Ala Gly Tyr Ser Ala Ser Lys Ala Ala Val Ser
145 150 155 160
Ala Leu Thr Arg Ala Ala Ala Leu Ser Cys Arg Lys Gln Gly Tyr Ala
165 170 175
Ile Arg Val Asn Ser Ile His Pro Asp Gly Ile Tyr Thr Pro Met Met
180 185 190
Gln Ala Ser Leu Pro Lys Gly Val Ser Lys Glu Met Val Leu His Asp
195 200 205
Pro Lys Leu Asn Arg Ala Gly Arg Ala Tyr Met Pro Glu Arg Ile Ala
210 215 220
Gln Leu Val Leu Phe Leu Ala Ser Asp Glu Ser Ser Val Met Ser Gly
225 230 235 240
Ser Glu Leu His Ala Asp Asn Ser Ile Leu Gly Met Gly Leu
245 250

Claims (8)

1.一种右旋樟脑在酮还原酶的作用下制备右旋龙脑的方法,其特征在于,反应式为:
Figure 783367DEST_PATH_IMAGE001
所述酮还原酶的DNA序列为SEQ ID No.1、SEQ ID No.2和SEQ ID No.3所示的任一序列,或者,所述酮还原酶的蛋白质序列为SEQ ID No.4、SEQ ID No.5和SEQ ID No.6所示的任一序列。
2.如权利要求1所述的方法,其具体步骤包括:取右旋樟脑置于缓冲溶液中,再向其中加入所述酮还原酶,得到混合溶液,使所述混合溶液在20-40℃下反应,得所述右旋龙脑。
3.如权利要求2所述的方法,其特征在于,所述缓冲溶液为pH值为6.0-8.0,浓度为0.01-0.5mol/L的PBS缓冲溶液。
4.如权利要求1-3任一项所述的方法,其特征在于,所述右旋樟脑和酮还原酶的重量比为20:1 - 50:1。
5.如权利要求1-3任一项所述的方法,其特征在于,向所述缓冲溶液中加入右旋樟脑时,还加入葡萄糖、异丙醇、甲酸铵中的一种。
6.如权利要求5所述的方法,其特征在于,在所述混合溶液中,右旋樟脑与葡萄糖的摩尔比为1:(1.2-1.5);右旋樟脑与异丙醇的摩尔比为1:(5-10);右旋樟脑与甲酸铵的摩尔比为1:(1.2-1.5)。
7.如权利要求1-3任一项所述的方法,其特征在于,向所述缓冲溶液中加入所述酮还原酶后,还加入葡萄糖脱氢酶、NADP+、甲酸脱氢酶中的一种或多种。
8.如权利要求7所述的方法,其特征在于,所述葡萄糖脱氢酶采购自苏州引航生物科技有限公司,商品编号YH1901,所述甲酸脱氢酶采购自苏州引航生物科技有限公司,商品编号YH1805。
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101284876A (zh) * 2008-05-28 2008-10-15 武汉大学 融合蛋白Penharpin及制备方法和用途
CN102492668A (zh) * 2011-11-29 2012-06-13 华东理工大学 一种羰基还原酶及其基因和在不对称还原羰基化合物中的应用
CN103074360A (zh) * 2012-12-13 2013-05-01 长春理工大学 睾丸酮丛毛单胞菌3,17β-羟基类固醇脱氢酶基因增强菌株构建及应用

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN85102398B (zh) * 1985-04-01 1986-11-26 中国科学院广州化学研究所 直接催化水合法制备龙脑
CN102876734B (zh) * 2012-10-30 2014-01-01 华东理工大学 一种羰基还原酶、基因及其在不对称还原前手性羰基化合物中的应用

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101284876A (zh) * 2008-05-28 2008-10-15 武汉大学 融合蛋白Penharpin及制备方法和用途
CN102492668A (zh) * 2011-11-29 2012-06-13 华东理工大学 一种羰基还原酶及其基因和在不对称还原羰基化合物中的应用
CN103074360A (zh) * 2012-12-13 2013-05-01 长春理工大学 睾丸酮丛毛单胞菌3,17β-羟基类固醇脱氢酶基因增强菌株构建及应用

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"hypothetical protein PENSTE_c007G06744 [Penicillium steckii] ACCESSION NO: OQE24597";Nielsen,J.C.et al.;《GENBANK DATABASE》;20170324;参见FEATURES和ORIGIN *
"Molecular cloning and functional identification of a novel borneoldehydrogenase from Artemisia annua L.";Na Tian et al.;《Industrial Crops and Products》;20150908;第77卷;参见190页右栏第1段-191页左栏的1段 *
"PBS 缓冲液配制";无天20101225;《百度文库》;20161018;参见第1页第1-20段 *
"Practical chiral alcohol manufacture using ketoreductases";Gjalt W Huisman, Jack Liang and Anke Krebber;《 Current Opinion in Chemical Biology》;20100112;第14卷(第2期);参见摘要,第123页左栏第1段-右栏第1段,表1-3,图1 *
"樟脑不对称合成右旋龙脑";王宁辉;《中国优秀博硕士学位论文全文数据库(硕士)工程科技I辑》;20070115(第1期);参见摘要,1.1. 2 、1. 1. 3. 3 、1. 2. 3. 5. 2 、3.1-4.7部分 *

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