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序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
21	GENES AND PROCESSES FOR THE PRODUCTION OF CLAVINE-TYPE ALKALOIDS	US14421872	2013-08-13	US20150211036A1	2015-07-30	Michael Naesby; Christophe Folly; Curt Aimé Friis Nielsen; Anaelle Hatsch; Markus Schwab; Oskar Zelder; Stefan Haefner; Hartwig Schroeder; Birgit Hoff; Andrea Molt; Klaus Ditrich; Michael Breuer; Holger Hartmann; Karsten Koerber
Microorganisms and processes for the recombinant manufacture of clavine-type alkaloids such as cycloclavine, festuclavine, agroclavine, chanoclavine and chanoclavine aldehyde, as well as polypeptides, polynucleotides and vectors comprising such polynucleotides which can be applied in a method for the manufacture of clavine-type alkaloids are provided.
22	Aromatic prenyltransferase from Cannabis	US13389815	2010-08-04	US08884100B2	2014-11-11	Jonathan E. Page; Zakia Boubakir
Nucleic acid molecules from Cannabis sativa (cannabis, hemp, marijuana) have been isolated and characterized, and encode polypeptides having aromatic prenyltransferase activity. Specifically, the enzyme, CsPT1, is a geranylpyrophosphate olivetolate geranyltransferase, active in the cannabinoid biosynthesis step of prenylation of olivetolic acid to form cannabigerolic acid (CBGA). Expression or over-expression of the nucleic acids alters levels of cannabinoid compounds. The polypeptides may be used in vivo or in vitro to produce cannabinoid compounds.
23	METHOD FOR PRODUCING PYRIPYROPENE	US13575159	2011-01-19	US20130023017A1	2013-01-24	Hiroyuki Anzai; Kentaro Yamamoto; Kazuhiko Oyama; Mariko Tsuchida; Kimihiko Goto; Masaaki Mitomi
There is provided a method for culturing a microorganism in which a particular polynucleotide or a recombinant vector comprising it/them is introduced with an intermediate compound necessary for biosynthesis of pyripyropene. A. The method of the present invention allows for the production of pyripyropene.
24	メバロン酸、イソプレノイド前駆体、及びイソプレンの産生におけるホスホケトラーゼの使用	JP2014534810	2012-10-05	JP6420147B2	2018-11-07	ベック、ザッカリー・キュー; エリオット、アンドリュー・シー; ペレス、キャロライン・エム; ヴァヴィライン、ドミートリ・ヴィ

25	サイトカイニンシンターゼ酵素、構築物、および関連する方法	JP2016567970	2015-05-21	JP2017522001A	2017-08-10	ティー．ビーソン，アイヴィ，ウィリアム; ジョンウェストフォール，パトリック
本開示は、2つのドメイン:イソペンテニル転移(IPT)様ドメイン、およびサイトカイニンヌクレオチドホスホリボヒドロラーゼ(PRH)様ドメインを有する新たなクラスのサイトカイニン生合成酵素であるサイトカイニンシンターゼに関する。本発明は、サイトカイニンシンターゼの組換え産生のための組成物および方法、サイトカイニンシンターゼを含む宿主細胞および形質転換体、ならびに開示されるサイトカイニンシンターゼを含む組成物および製剤を提供する。
26	ピリピロペンの製造法	JP2011551815	2011-01-19	JP5898960B2	2016-04-06	安西弘行; 山本憲太朗; 尾山和彦; 土田麻里子; 後藤公彦; 三冨正明

27	ピリピロペン生合成遺伝子群およびマーカー遺伝子を含む核酸構築物	JP2011551816	2011-01-19	JP5864267B2	2016-02-17	相原智; 隅田奈緒美; 村島弘一郎; 矢内耕二; 安西弘行; 山本憲太朗

28	クラビン類アルカロイドを製造するための遺伝子およびプロセス	JP2015527987	2013-08-13	JP2015530879A	2015-10-29	ゼルダー，オスカー; ヘフナー，シュテファン; シュレーダー，ハルトヴィッヒ; ホフ，ビルジット; モルト，アンドレア; ディトリッヒ，クラウス; ブロイアー，ミヒャエル; ハルトマン，ホルガー; ケルバー，カルステン; ネスビー，ミヒャエル; シュワブ，マルクス; アイムフリスニールセン，クルト; フォーリー，クリストフ; ハッシュ，アネル
シクロクラビン、フェスツクラビン、アグロクラビン、カノクラビン、およびカノクラビンアルデヒドなどのクラビン類アルカロイドを、組換え技術により製造するための微生物およびプロセス、ならびに、クラビン類アルカロイドを製造するための方法に適用することができるポリペプチド、ポリヌクレオチド、およびそうしたポリヌクレオチドを含有するベクターを提供する。【選択図】なし
29	Production of Tetrahydrocannabinolic Acid in Yeast	US16122702	2018-09-05	US20180371507A1	2018-12-27	Jason L. Poulos; Anthony N. Farnia
Exemplary embodiments provided herein include genetically engineering microorganisms, such as yeast or bacteria, to produce cannabinoids by inserting genes that produce the appropriate enzymes for the metabolic production of a desired compound.
30	Production of cannabidiolic acid in yeast	US15815651	2017-11-16	US10093949B2	2018-10-09	Jason L. Poulos; Anthony N. Farnia
Exemplary embodiments provided herein include genetically engineering microorganisms, such as yeast or bacteria, to produce cannabinoids by inserting genes that produce the appropriate enzymes for the metabolic production of a desired compound.
31	Genes and processes for the production of clavine-type alkaloids	US14421872	2013-08-13	US09828617B2	2017-11-28	Michael Naesby; Christophe Folly; Curt Aimé Friis Nielsen; Anaelle Hatsch; Markus Schwab; Oskar Zelder; Stefan Haefner; Hartwig Schroeder; Birgit Hoff; Andrea Molt; Klaus Ditrich; Michael Breuer; Holger Hartmann; Karsten Koerber
Microorganisms and processes for the recombinant manufacture of clavine-type alkaloids such as cycloclavine, festuclavine, agroclavine, chanoclavine and chanoclavine aldehyde, as well as polypeptides, polynucleotides and vectors comprising such polynucleotides which can be applied in a method for the manufacture of clavine-type alkaloids are provided.
32	METHODS OF PRODUCTION OF PRODUCTS OF METABOLIC PATHWAYS	US15611803	2017-06-02	US20170268030A1	2017-09-21	Ron MILO; Lior ZELCBUCH; Niv ANTONOVSKY
A plurality of isolated polynucleotide sequences encoding enzymes of the astaxanthin pathway is disclosed. The polynucleotides include: (i) a polynucleotide which encodes Phytoene dehydrogenase (crtI) and a first transcriptional regulatory sequence; (ii) a polynucleotide which encodes Beta-lycopene cyclase (lcy-B) and a second transcriptional regulatory sequence; (iii) a polynucleotide which encodes Beta-carotene ketolase (crtW) and a third transcriptional regulatory sequence; and wherein the first, second and third regulatory sequence are selected such that the expression of the Icy-B and the crtW is greater than a level of expression of the crtI. Methods of generating astaxanthin using the plurality of polynucleotide are also disclosed as well as bacterial cells comprising high levels of astaxanthin.
33	Aromatic prenyltransferase from cannabis	US14510232	2014-10-09	US09765308B2	2017-09-19	Jonathan E. Page; Zakia Boubakir
Nucleic acid molecules from cannabis has been isolated and characterized and encode polypeptides having aromatic prenyltransferase activity. Expression or over-expression of the nucleic acids alters levels of cannabinoid compounds. The polypeptides may be used in vivo or in vitro to produce cannabinoid compounds.
34	Vectors and strains for producing myrcene and method of producing myrcene using the same	US14950425	2015-11-24	US09719095B2	2017-08-01	Han Min Woo; Eun Mi Kim; Youngsoon Um; Gyeongtaek Gong; Sun Mi Lee; Yunje Kim
Disclosed herein are an expression vector capable of expressing myrcene, an Escherichia coli strain transformed with the vector and having improved capability of producing myrcene and a method for producing myrcene and a method for recycling glycerol using the same. In an aspect, the transformed Escherichia coli strain of the present disclosure can produce myrcene with high purity on a large scale using glycerol or glucose as a carbon source. Also, the Escherichia coli strain of the present disclosure is economical and environment-friendly because it can produce high value-added myrcene using waste glycerol as a carbon source. In addition, the strongly volatile myrcene can be produced and isolated at the same time.
35	UTILIZATION OF PHOSPHOKETOLASE IN THE PRODUCTION OF MEVALONATE, ISOPRENOID PRECURSORS, AND ISOPRENE	US15279184	2016-09-28	US20170198311A1	2017-07-13	Zachary Q. BECK; Caroline M. PERES; Dmitrii V. VAVILINE; Andrew C. ELIOT
The invention provides for methods for the production of mevalonate, isoprene, isoprenoid precursor molecules, and/or isoprenoids in cells via the heterologous expression of phosphoketolase enzymes.
36	Methods for Recombinant Production of Saffron Compounds	US15123198	2015-03-06	US20170067063A1	2017-03-09	A.S. Sathish Kumar
Recombinant microorganisms and methods for producing saffron compounds including crocetin, crocetin dialdehyde, crocin or picrocrocin are disclosed herein.
37	VECTORS AND STRAINS FOR PRODUCING MYRCENE AND METHOD OF PRODUCING MYRCENE USING THE SAME	US14950425	2015-11-24	US20170009240A1	2017-01-12	Han Min WOO; Eun Mi KIM; Youngsoon UM; Gyeongtaek GONG; Sun Mi LEE; Yunje KIM
Disclosed herein are an expression vector capable of expressing myrcene, an Escherichia coli strain transformed with the vector and having improved capability of producing myrcene and a method for producing myrcene and a method for recycling glycerol using the same. In an aspect, the transformed Escherichia coli strain of the present disclosure can produce myrcene with high purity on a large scale using glycerol or glucose as a carbon source. Also, the Escherichia coli strain of the present disclosure is economical and environment-friendly because it can produce high value-added myrcene using waste glycerol as a carbon source. In addition, the strongly volatile myrcene can be produced and isolated at the same time.
38	Utilization of phosphoketolase in the production of mevalonate, isoprenoid precursors, and isoprene	US14625487	2015-02-18	US09493791B2	2016-11-15	Zachary Q. Beck; Andrew C. Eliot; Caroline M. Peres; Dmitrii V. Vaviline
The invention provides for methods for the production of mevalonate, isoprene, isoprenoid precursor molecules, and/or isoprenoids in cells via the heterologous expression of phosphoketolase enzymes.
39	VECTOR COMPRISING SPECIFIC PROMOTER AND GENE ENCODING SPECIFIC PROTEIN, TRANSGENIC PLANT INTO WHICH THE VECTOR HAS BEEN INTRODUCED, AND METHOD FOR IMPROVING POLYISOPRENOID PRODUCTION BY INTRODUCING THE VECTOR INTO PLANT	US15018504	2016-02-08	US20160244774A1	2016-08-25	Yukino INOUE; Akari OKADA; Haruhiko YAMAGUCHI; Satoshi KURODA
Provided is a vector capable of improving polyisoprenoid production through the introduction of the vector into a plant using gene recombination techniques. A vector comprising: a promoter of a gene encoding Hevein 2.1; and a gene encoding a protein involved in polyisoprenoid biosynthesis, the gene being functionally linked to the promoter.
40	CYTOKININ SYNTHASE ENZYMES, CONSTRUCTS, AND RELATED METHODS	US14718585	2015-05-21	US20160076010A1	2016-03-17	William T. Beeson, IV; Patrick John Westfall
The present disclosure relates to a new class of cytokinin biosynthetic enzymes, cytokinin synthases, which have two domains: an isopentenyl transfer (IPT)-like domain and a cytokinin nucleotide phosphoribohydrolase (PRH)-like domain. The invention provides compositions and methods for the recombinant production of cytokinin synthase, host cells and transformants that include the cytokinin synthases, as well as compositions and formulations that include the disclosed cytokinin synthase.

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