Metabolic engineering strategies for increasing lipid production in oleaginous yeast

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2015.

Bibliographic Details
Main Author: Silverman, Andrew Michael
Other Authors: Gregory N. Stephanopoulos.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2016
Subjects:
Online Access:http://hdl.handle.net/1721.1/103274
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author Silverman, Andrew Michael
author2 Gregory N. Stephanopoulos.
author_facet Gregory N. Stephanopoulos.
Silverman, Andrew Michael
author_sort Silverman, Andrew Michael
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description Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2015.
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spelling mit-1721.1/1032742019-04-11T13:18:29Z Metabolic engineering strategies for increasing lipid production in oleaginous yeast Silverman, Andrew Michael Gregory N. Stephanopoulos. Massachusetts Institute of Technology. Department of Chemical Engineering. Massachusetts Institute of Technology. Department of Chemical Engineering. Chemical Engineering. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2015. Page 11 out of sequence; inserted between page 4 and page 5. Page 209 blank. Cataloged from PDF version of thesis. Includes bibliographical references. Although petroleum and other fossil fuels have traditionally been used to fulfill our energy needs, rising concerns over energy security and the climate-changing effects of our continual greenhouse gas emissions have led to great interest in developing a domestic source of renewable fuel with low net carbon emissions. Biodiesel is an attractive option for replacing petroleum-based fuels used in the transportation sector due to its compatibility with existing infrastructure. Single cell oils from heterotrophic oleaginous microorganisms as a source of bio diesel allow for high productivity from a wide array of potential feedstocks, including agroindustrial and municipal waste streams. The goal of this work is to use the tools of rational metabolic engineering to improve lipid production in the non-conventional oleaginous yeast Yarrowia lipoytica on two representative carbon sources, glucose and acetate. Previous work in this area achieved considerable success with the simultaneous overexpression of the native acetyl-CoA carboxylase (ACC 1) and diacylglycerol acyltransferase (DGA2) genes; the resulting strain was used as a benchmark to evaluate our own efforts. We began with the compilation of a set of 44 genes and evaluated the effects of the individual overexpression of each gene on the ability of the resulting strain to produce lipids in fermentations of glucose and acetate. The genes tested here represent many different functions potentially important to lipid production, including the Kennedy pathway, fatty acid synthesis, central carbon metabolism, NADPH generation, regulation, and metabolite transport. Our results demonstrate that a diverse subset of gene overexpressions led to significant improvements in lipid production on at least one substrate. The largest improvements unsurprisingly came from overexpressing genes directly related to triacylglycerol synthesis, such as diacylglycerol acyltransferase DGAI, which on glucose increased the lipid titer, content and yield by 236%. 165%, and 246%, respectively, over our wild-type control strain, and the acylglycerolphosphate acyltransferase SLC1 gene, which increased titer/content/yield on glucose by 86%/73%/87% and on acetate by 99%/91%/151%. Significant improvements were also detected from genes that more indirectly effect lipogenesis, such as glycerol-3-phosphate dehydrogenase GPD (which produces head groups for triacylglycerol molecules) and the 6-phosphogluconolactoase SOL3 (catalyzing the middle step of the NADPH-producing oxidative pentose phosphate pathway). We next chose the aforementioned SLCl, GPD, and SOL3 genes for use in continued rational engineering of our benchmark strain due to the significance of their effects and the lack of redundancy in their likely mechanism of improving lipogenesis when overexpressed along with ACC I and DGA2. The results of this investigation indicate that the strain overexpressing ACC 1, DGA2,'and SLC 1 may be superior to our benchmark strain, increasing lipid content and yield by 24% and 20%, respectively, with a statistically equivalent titer on acetate. This strain produces the highest reported overall lipid yield of an oleaginous yeast on acetate, at 0.207 g lipids/g acetate. by Andrew Michael Silverman. Ph. D. 2016-06-22T17:54:59Z 2016-06-22T17:54:59Z 2015 2015 Thesis http://hdl.handle.net/1721.1/103274 951809726 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 209 pages application/pdf Massachusetts Institute of Technology
spellingShingle Chemical Engineering.
Silverman, Andrew Michael
Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title_full Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title_fullStr Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title_full_unstemmed Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title_short Metabolic engineering strategies for increasing lipid production in oleaginous yeast
title_sort metabolic engineering strategies for increasing lipid production in oleaginous yeast
topic Chemical Engineering.
url http://hdl.handle.net/1721.1/103274
work_keys_str_mv AT silvermanandrewmichael metabolicengineeringstrategiesforincreasinglipidproductioninoleaginousyeast