Cargando…
Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass
Despite the capacity to accumulate ~70% w/w of lipids, commercially produced unicellular green alga A. protothecoides may become compromised due to the high cost of phosphate fertilizers. To address this limitation A. protothecoides was selected for adaptation to conditions of 100× and 5× lower phos...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007911/ https://www.ncbi.nlm.nih.gov/pubmed/29920531 http://dx.doi.org/10.1371/journal.pone.0198953 |
_version_ | 1783333109968666624 |
---|---|
author | Park, Sang-Hyuck Kyndt, John Chougule, Kapeel Park, Jeong-Jin Brown, Judith K. |
author_facet | Park, Sang-Hyuck Kyndt, John Chougule, Kapeel Park, Jeong-Jin Brown, Judith K. |
author_sort | Park, Sang-Hyuck |
collection | PubMed |
description | Despite the capacity to accumulate ~70% w/w of lipids, commercially produced unicellular green alga A. protothecoides may become compromised due to the high cost of phosphate fertilizers. To address this limitation A. protothecoides was selected for adaptation to conditions of 100× and 5× lower phosphate and peptone, respectively, compared to ‘wild-type media’. The A. protothecoides showed initial signs of adaptation by 45–50 days, and steady state growth at ~100 days. The low phosphate (P)-adapted strain produced up to ~30% greater biomass, while total lipids (~10% w/w) remained about the same, compared to the wild-type strain. Metabolomic analyses indicated that the low P-adapted produced 3.3-fold more saturated palmitic acid (16:0) and 2.2-fold less linolenic acid (18:3), compared to the wild-type strain, resulting in an ~11% increase in caloric value, from 19.5kJ/g for the wild-type strain to 21.6kJ/g for the low P-adapted strain, due to the amounts and composition of certain saturated fatty acids, compared to the wild type strain. Biochemical changes in A. protothecoides adapted to lower phosphate conditions were assessed by comparative RNA-Seq analysis, which yielded 27,279 transcripts. Among them, 2,667 and 15 genes were significantly down- and up-regulated, at >999-fold and >3-fold (adjusted p-value <0.1), respectively. The expression of genes encoding proteins involved in cellular processes such as division, growth, and membrane biosynthesis, showed a trend toward down-regulation. At the genomic level, synonymous SNPs and Indels were observed primarily in coding regions, with the 40S ribosomal subunit gene harboring substantial SNPs. Overall, the adapted strain out-performed the wild-type strain by prioritizing the use of its limited phosphate supply for essential biological processes. The low P-adapted A. protothecoides is expected to be more economical to grow over the wild-type strain, based on overall greater productivity and caloric content, while importantly, also requiring 100-fold less phosphate. |
format | Online Article Text |
id | pubmed-6007911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60079112018-06-21 Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass Park, Sang-Hyuck Kyndt, John Chougule, Kapeel Park, Jeong-Jin Brown, Judith K. PLoS One Research Article Despite the capacity to accumulate ~70% w/w of lipids, commercially produced unicellular green alga A. protothecoides may become compromised due to the high cost of phosphate fertilizers. To address this limitation A. protothecoides was selected for adaptation to conditions of 100× and 5× lower phosphate and peptone, respectively, compared to ‘wild-type media’. The A. protothecoides showed initial signs of adaptation by 45–50 days, and steady state growth at ~100 days. The low phosphate (P)-adapted strain produced up to ~30% greater biomass, while total lipids (~10% w/w) remained about the same, compared to the wild-type strain. Metabolomic analyses indicated that the low P-adapted produced 3.3-fold more saturated palmitic acid (16:0) and 2.2-fold less linolenic acid (18:3), compared to the wild-type strain, resulting in an ~11% increase in caloric value, from 19.5kJ/g for the wild-type strain to 21.6kJ/g for the low P-adapted strain, due to the amounts and composition of certain saturated fatty acids, compared to the wild type strain. Biochemical changes in A. protothecoides adapted to lower phosphate conditions were assessed by comparative RNA-Seq analysis, which yielded 27,279 transcripts. Among them, 2,667 and 15 genes were significantly down- and up-regulated, at >999-fold and >3-fold (adjusted p-value <0.1), respectively. The expression of genes encoding proteins involved in cellular processes such as division, growth, and membrane biosynthesis, showed a trend toward down-regulation. At the genomic level, synonymous SNPs and Indels were observed primarily in coding regions, with the 40S ribosomal subunit gene harboring substantial SNPs. Overall, the adapted strain out-performed the wild-type strain by prioritizing the use of its limited phosphate supply for essential biological processes. The low P-adapted A. protothecoides is expected to be more economical to grow over the wild-type strain, based on overall greater productivity and caloric content, while importantly, also requiring 100-fold less phosphate. Public Library of Science 2018-06-19 /pmc/articles/PMC6007911/ /pubmed/29920531 http://dx.doi.org/10.1371/journal.pone.0198953 Text en © 2018 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Park, Sang-Hyuck Kyndt, John Chougule, Kapeel Park, Jeong-Jin Brown, Judith K. Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title | Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title_full | Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title_fullStr | Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title_full_unstemmed | Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title_short | Low-phosphate-selected Auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
title_sort | low-phosphate-selected auxenochlorella protothecoides redirects phosphate to essential pathways while producing more biomass |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007911/ https://www.ncbi.nlm.nih.gov/pubmed/29920531 http://dx.doi.org/10.1371/journal.pone.0198953 |
work_keys_str_mv | AT parksanghyuck lowphosphateselectedauxenochlorellaprotothecoidesredirectsphosphatetoessentialpathwayswhileproducingmorebiomass AT kyndtjohn lowphosphateselectedauxenochlorellaprotothecoidesredirectsphosphatetoessentialpathwayswhileproducingmorebiomass AT chougulekapeel lowphosphateselectedauxenochlorellaprotothecoidesredirectsphosphatetoessentialpathwayswhileproducingmorebiomass AT parkjeongjin lowphosphateselectedauxenochlorellaprotothecoidesredirectsphosphatetoessentialpathwayswhileproducingmorebiomass AT brownjudithk lowphosphateselectedauxenochlorellaprotothecoidesredirectsphosphatetoessentialpathwayswhileproducingmorebiomass |