語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Characterization of Nannochloropsis ...
~
Michigan State University.
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development./
作者:
Poliner, Eric.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
面頁冊數:
218 p.
附註:
Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.
Contained By:
Dissertation Abstracts International79-03B(E).
標題:
Molecular biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10685216
ISBN:
9780355515473
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development.
Poliner, Eric.
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 218 p.
Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.
Thesis (Ph.D.)--Michigan State University, 2017.
Nannochloropsis is a genus of fast-growing microalgae that have a high lipid content. Nannochloropsis species have a high triacylglycerol (TAG) content and contain a large amount of the omega-3 long-chain polyunsaturated fatty acid, eicosapentaenoic acid (EPA). There is a growing interest in Nannochloropsis species as models for the study of microalga lipid metabolism and as a platform for synthetic biology. Genome sequences are available for several species, and genetic engineering techniques are being introduced. In this study, I developed a new generation of transgenic vectors for gene stacking and marker-free gene disruption in Nannochloropsis oceanica CCMP1779. These tools enable gene specific studies and were applied to investigate a lipid biosynthetic pathway that is co-expressed under different light conditions. As for all photosynthetic organisms, light plays an important role in driving metabolism and regulation by photosensing in Nannochloropsis species. Each day photosynthetic organisms must maximize their energy capture during the day and be able to sustain themselves during the night. Nannochloropsis cultures synchronize cell division during a light:dark cycle, with cell division occurring at night, along with the usage of stored metabolites that are accumulated during the day. RNA-sequencing measures global transcript abundance, that ultimately might lead to changes in enzymatic activity, metabolism and physiology. I investigated the role of transcriptional regulation on metabolite levels and cell physiology using RNA-sequencing. In the study I found coordination between cell growth, triacylglycerol and hexose content, and transcript abundance of the genes in relevant pathways. Briefly anabolic processes were phased to the light period and catabolic processes phased to the dark period. Furthermore, promoters for transgenic expression were chosen based on transcriptomic measurements gathered in this study. Eicosapentaenoic acid is a high-value fatty acid that is a necessary nutrient for humans, with a biosynthetic pathway consisting of 5 fatty acids desaturases (FADs) and a fatty acid elongase (FAE). Interestingly, the genes of this biosynthetic pathway were strongly co-expressed during light:dark cycles, and I set out to characterize the pathway. Expression of isolated cDNAs in S. cerevisiae resulted in the production of the expected long-chain polyunsaturated fatty acids (LC-PUFAs), and ultimately EPA when all 4 LC-PUFA FADs and an FAE were co-expressed. Selected FADs were overexpressed in N. oceanica and resulted in increased LC-PUFA and EPA content. CRISPR/Cas9 is a potent tool for gene editing. The RNA-guided nuclease, Cas9, was tested as a fusion with green fluorescent protein (GFP) and NanoLuciferase (Nlux) reporters, and the Cas9-Nlux fusion was readily detectable for efficient screening of transformants for recombinant protein production. Single-guide RNAs (sgRNAs) when fused to 5' and 3' self-cleaving ribozymes efficiently targeted genes. The two components of the system were expressed from a bidirectional promoter. N. oceanica is capable of expressing transgenes from circular episomal DNA, and an episomal CRISPR construct was generated. The nitrate reductase gene was targeted and the mutants generated with frame-shifts in the coding sequence were unable to grow on nitrate. When antibiotic selection was removed, the episome was lost, and a mutant line that was "cured" of the episome was isolated. These tools are being utilized for gene specific studies in N. oceanica.
ISBN: 9780355515473Subjects--Topical Terms:
583443
Molecular biology.
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development.
LDR
:04578nam a2200301 4500
001
890764
005
20180727091503.5
008
180907s2017 ||||||||||||||||| ||eng d
020
$a
9780355515473
035
$a
(MiAaPQ)AAI10685216
035
$a
(MiAaPQ)grad.msu:15746
035
$a
AAI10685216
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Poliner, Eric.
$3
1148664
245
1 0
$a
Characterization of Nannochloropsis oceanica CCMP1779 Grown in Light:Dark Cycles Informs Genetic Engineering Tool Development.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2017
300
$a
218 p.
500
$a
Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.
500
$a
Advisers: Eva M. Farre; Christoph Benning.
502
$a
Thesis (Ph.D.)--Michigan State University, 2017.
520
$a
Nannochloropsis is a genus of fast-growing microalgae that have a high lipid content. Nannochloropsis species have a high triacylglycerol (TAG) content and contain a large amount of the omega-3 long-chain polyunsaturated fatty acid, eicosapentaenoic acid (EPA). There is a growing interest in Nannochloropsis species as models for the study of microalga lipid metabolism and as a platform for synthetic biology. Genome sequences are available for several species, and genetic engineering techniques are being introduced. In this study, I developed a new generation of transgenic vectors for gene stacking and marker-free gene disruption in Nannochloropsis oceanica CCMP1779. These tools enable gene specific studies and were applied to investigate a lipid biosynthetic pathway that is co-expressed under different light conditions. As for all photosynthetic organisms, light plays an important role in driving metabolism and regulation by photosensing in Nannochloropsis species. Each day photosynthetic organisms must maximize their energy capture during the day and be able to sustain themselves during the night. Nannochloropsis cultures synchronize cell division during a light:dark cycle, with cell division occurring at night, along with the usage of stored metabolites that are accumulated during the day. RNA-sequencing measures global transcript abundance, that ultimately might lead to changes in enzymatic activity, metabolism and physiology. I investigated the role of transcriptional regulation on metabolite levels and cell physiology using RNA-sequencing. In the study I found coordination between cell growth, triacylglycerol and hexose content, and transcript abundance of the genes in relevant pathways. Briefly anabolic processes were phased to the light period and catabolic processes phased to the dark period. Furthermore, promoters for transgenic expression were chosen based on transcriptomic measurements gathered in this study. Eicosapentaenoic acid is a high-value fatty acid that is a necessary nutrient for humans, with a biosynthetic pathway consisting of 5 fatty acids desaturases (FADs) and a fatty acid elongase (FAE). Interestingly, the genes of this biosynthetic pathway were strongly co-expressed during light:dark cycles, and I set out to characterize the pathway. Expression of isolated cDNAs in S. cerevisiae resulted in the production of the expected long-chain polyunsaturated fatty acids (LC-PUFAs), and ultimately EPA when all 4 LC-PUFA FADs and an FAE were co-expressed. Selected FADs were overexpressed in N. oceanica and resulted in increased LC-PUFA and EPA content. CRISPR/Cas9 is a potent tool for gene editing. The RNA-guided nuclease, Cas9, was tested as a fusion with green fluorescent protein (GFP) and NanoLuciferase (Nlux) reporters, and the Cas9-Nlux fusion was readily detectable for efficient screening of transformants for recombinant protein production. Single-guide RNAs (sgRNAs) when fused to 5' and 3' self-cleaving ribozymes efficiently targeted genes. The two components of the system were expressed from a bidirectional promoter. N. oceanica is capable of expressing transgenes from circular episomal DNA, and an episomal CRISPR construct was generated. The nitrate reductase gene was targeted and the mutants generated with frame-shifts in the coding sequence were unable to grow on nitrate. When antibiotic selection was removed, the episome was lost, and a mutant line that was "cured" of the episome was isolated. These tools are being utilized for gene specific studies in N. oceanica.
590
$a
School code: 0128.
650
4
$a
Molecular biology.
$3
583443
650
4
$a
Cellular biology.
$3
1148666
690
$a
0307
690
$a
0379
710
2
$a
Michigan State University.
$b
Cell and Molecular Biology.
$3
1148665
773
0
$t
Dissertation Abstracts International
$g
79-03B(E).
790
$a
0128
791
$a
Ph.D.
792
$a
2017
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10685216
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入