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公开(公告)号:US09719122B2
公开(公告)日:2017-08-01
申请号:US14415612
申请日:2013-07-17
Applicant: Yeda Research and Development Co. Ltd.
Inventor: Ron Milo , Lior Zelcbuch , Niv Antonovsky
CPC classification number: C12P23/00 , C12N9/0004 , C12N9/001 , C12N9/0073 , C12N9/1085 , C12N9/90 , C12N15/52 , C12N15/67 , C12N15/70 , C12Y114/13129 , C12Y205/01 , C12Y205/01029 , C12Y505/01019
Abstract: 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.
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公开(公告)号:US20150211040A1
公开(公告)日:2015-07-30
申请号:US14415612
申请日:2013-07-17
Applicant: Yeda Research and Development Co. Ltd.
Inventor: Ron Milo , Lior Zelcbuch , Niv Antonovsky
CPC classification number: C12P23/00 , C12N9/0004 , C12N9/001 , C12N9/0073 , C12N9/1085 , C12N9/90 , C12N15/52 , C12N15/67 , C12N15/70 , C12Y114/13129 , C12Y205/01 , C12Y205/01029 , C12Y505/01019
Abstract: 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.
Abstract translation: 公开了编码虾青素途径酶的多个分离的多核苷酸序列。 多核苷酸包括:(i)编码叶绿素脱氢酶(crtI)和第一转录调控序列的多核苷酸; (ii)编码β-番茄红素环化酶(lcy-B)和第二转录调控序列的多核苷酸; (iii)编码β-胡萝卜素酮醇酶(crtW)和第三转录调节序列的多核苷酸; 并且其中选择第一,第二和第三调节序列使得Icy-B和crtW的表达大于crtI的表达水平。 还公开了使用多种多核苷酸产生虾青素的方法以及包含高水平的虾青素的细菌细胞。
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公开(公告)号:US10294482B2
公开(公告)日:2019-05-21
申请号:US15312734
申请日:2015-05-21
Applicant: Yeda Research and Development Co. Ltd.
Inventor: Ron Milo , Niv Antonovsky , Elad Noor , Arren Bar-Even , Yehudit Zohar , Lior Zelcbuch , Shmuel Gleizer , Shira Amram
IPC: C12N15/70 , C12N15/52 , C12N15/74 , C07K14/195 , C07K14/245 , C12N1/20 , C12N9/04 , C12N9/10 , C12N9/12 , C12N9/88 , C12N9/90
Abstract: A microorganism which is genetically modified so that it produces a first essential biomass precursor by metabolizing CO2 using a recombinant carbon fixation enzyme is disclosed. The microorganism produces a second biomass precursor by metabolizing an organic carbon source and not by metabolizing CO2. The microorganism does not use the organic carbon source for producing the first essential biomass precursor.
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公开(公告)号:US12031138B2
公开(公告)日:2024-07-09
申请号:US16362897
申请日:2019-03-25
Applicant: Yeda Research and Development Co. Ltd.
Inventor: Ron Milo , Niv Antonovsky , Elad Noor , Arren Bar-Even , Yehudit Zohar , Lior Zelcbuch , Shmuel Gleizer , Shira Amram
IPC: C12N15/70 , C07K14/195 , C07K14/245 , C12N1/20 , C12N9/04 , C12N9/10 , C12N9/12 , C12N9/88 , C12N9/90
CPC classification number: C12N15/70 , C07K14/195 , C07K14/245 , C12N1/20 , C12N9/0006 , C12N9/1025 , C12N9/1205 , C12N9/88 , C12N9/90 , C12Y101/01049 , C12Y203/03009 , C12Y207/01011 , C12Y207/01019 , C12Y401/01039 , C12Y402/01011 , C12Y504/02
Abstract: A microorganism which is genetically modified so that it produces a first essential biomass precursor by metabolizing CO2 using a recombinant carbon fixation enzyme is disclosed. The microorganism produces a second biomass precursor by metabolizing an organic carbon source and not by metabolizing CO2. The microorganism does not use the organic carbon source for producing the first essential biomass precursor.
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公开(公告)号:US10053712B2
公开(公告)日:2018-08-21
申请号:US15101097
申请日:2014-12-10
Applicant: Yeda Research and Development Co. Ltd.
Inventor: Arren Bar-Even , Ron Milo , Elad Noor , Lior Zelcbuch
IPC: C12P7/40 , C12N1/20 , C12N9/10 , C12N15/52 , C12P5/00 , C12P5/02 , C12P7/06 , C12P7/16 , C12P7/26 , C12P7/64
CPC classification number: C12P7/40 , C12N1/20 , C12N9/1029 , C12N15/52 , C12P5/007 , C12P5/023 , C12P5/026 , C12P7/06 , C12P7/16 , C12P7/26 , C12P7/649 , C12Y203/01054 , Y02E50/17 , Y02E50/343
Abstract: An isolated microorganism is disclosed being genetically modified to express pyruvate formate lyase (PFL) or 2-ketobutyrate formate lyase, wherein acetyl-CoA of the microorganism is converted to pyruvate in the presence of formate in a single step reaction, wherein the net flux of the reaction is in the direction of pyruvate synthesis.Uses of the microorganism and products comprising same are also disclosed.
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