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Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study
Cellular metabolite analyses by (13)C-NMR showed that C. reinhardtii cells assimilate acetate at a faster rate in heterotrophy than in mixotrophy. While heterotrophic cells produced bicarbonate and CO(2) (aq), mixotrophy cells produced bicarbonate alone as predominant metabolite. Experiments with si...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160175/ https://www.ncbi.nlm.nih.gov/pubmed/25207648 http://dx.doi.org/10.1371/journal.pone.0106457 |
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author | Singh, Himanshu Shukla, Manish R. Chary, Kandala V. R. Rao, Basuthkar J. |
author_facet | Singh, Himanshu Shukla, Manish R. Chary, Kandala V. R. Rao, Basuthkar J. |
author_sort | Singh, Himanshu |
collection | PubMed |
description | Cellular metabolite analyses by (13)C-NMR showed that C. reinhardtii cells assimilate acetate at a faster rate in heterotrophy than in mixotrophy. While heterotrophic cells produced bicarbonate and CO(2) (aq), mixotrophy cells produced bicarbonate alone as predominant metabolite. Experiments with singly (13)C-labelled acetate ((13)CH(3)-COOH or CH(3)-(13)COOH) supported that both the (13)C nuclei give rise to bicarbonate and CO(2) (aq). The observed metabolite(s) upon further incubation led to the production of starch and triacylglycerol (TAG) in mixotrophy, whereas in heterotrophy the TAG production was minimal with substantial accumulation of glycerol and starch. Prolonged incubation up to eight days, without the addition of fresh acetate, led to an increased TAG production at the expense of bicarbonate, akin to that of nitrogen-starvation. However, such TAG production was substantially high in mixotrophy as compared to that in heterotrophy. Addition of mitochondrial un-coupler blocked the formation of bicarbonate and CO(2) (aq) in heterotrophic cells, even though acetate uptake ensued. Addition of PSII-inhibitor to mixotrophic cells resulted in partial conversion of bicarbonate into CO(2) (aq), which were found to be in equilibrium. In an independent experiment, we have monitored assimilation of bicarbonate via photoautotrophy and found that the cells indeed produce starch and TAG at a much faster rate as compared to that in mixotrophy and heterotrophy. Further, we noticed that the accumulation of starch is relatively more as compared to TAG. Based on these observations, we suggest that acetate assimilation in C. reinhardtii does not directly lead to TAG formation but via bicarbonate/CO(2) (aq) pathways. Photoautotrophic mode is found to be the best growth condition for the production of starch and TAG and starch in C. reinhardtii. |
format | Online Article Text |
id | pubmed-4160175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41601752014-09-12 Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study Singh, Himanshu Shukla, Manish R. Chary, Kandala V. R. Rao, Basuthkar J. PLoS One Research Article Cellular metabolite analyses by (13)C-NMR showed that C. reinhardtii cells assimilate acetate at a faster rate in heterotrophy than in mixotrophy. While heterotrophic cells produced bicarbonate and CO(2) (aq), mixotrophy cells produced bicarbonate alone as predominant metabolite. Experiments with singly (13)C-labelled acetate ((13)CH(3)-COOH or CH(3)-(13)COOH) supported that both the (13)C nuclei give rise to bicarbonate and CO(2) (aq). The observed metabolite(s) upon further incubation led to the production of starch and triacylglycerol (TAG) in mixotrophy, whereas in heterotrophy the TAG production was minimal with substantial accumulation of glycerol and starch. Prolonged incubation up to eight days, without the addition of fresh acetate, led to an increased TAG production at the expense of bicarbonate, akin to that of nitrogen-starvation. However, such TAG production was substantially high in mixotrophy as compared to that in heterotrophy. Addition of mitochondrial un-coupler blocked the formation of bicarbonate and CO(2) (aq) in heterotrophic cells, even though acetate uptake ensued. Addition of PSII-inhibitor to mixotrophic cells resulted in partial conversion of bicarbonate into CO(2) (aq), which were found to be in equilibrium. In an independent experiment, we have monitored assimilation of bicarbonate via photoautotrophy and found that the cells indeed produce starch and TAG at a much faster rate as compared to that in mixotrophy and heterotrophy. Further, we noticed that the accumulation of starch is relatively more as compared to TAG. Based on these observations, we suggest that acetate assimilation in C. reinhardtii does not directly lead to TAG formation but via bicarbonate/CO(2) (aq) pathways. Photoautotrophic mode is found to be the best growth condition for the production of starch and TAG and starch in C. reinhardtii. Public Library of Science 2014-09-10 /pmc/articles/PMC4160175/ /pubmed/25207648 http://dx.doi.org/10.1371/journal.pone.0106457 Text en © 2014 Singh 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Singh, Himanshu Shukla, Manish R. Chary, Kandala V. R. Rao, Basuthkar J. Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title | Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title_full | Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title_fullStr | Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title_full_unstemmed | Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title_short | Acetate and Bicarbonate Assimilation and Metabolite Formation in Chlamydomonas reinhardtii: A (13)C-NMR Study |
title_sort | acetate and bicarbonate assimilation and metabolite formation in chlamydomonas reinhardtii: a (13)c-nmr study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160175/ https://www.ncbi.nlm.nih.gov/pubmed/25207648 http://dx.doi.org/10.1371/journal.pone.0106457 |
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