Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Himanshu, Shukla, Manish R., Chary, Kandala V. R., Rao, Basuthkar J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
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
_version_ 1782334347556159488
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
work_keys_str_mv AT singhhimanshu acetateandbicarbonateassimilationandmetaboliteformationinchlamydomonasreinhardtiia13cnmrstudy
AT shuklamanishr acetateandbicarbonateassimilationandmetaboliteformationinchlamydomonasreinhardtiia13cnmrstudy
AT charykandalavr acetateandbicarbonateassimilationandmetaboliteformationinchlamydomonasreinhardtiia13cnmrstudy
AT raobasuthkarj acetateandbicarbonateassimilationandmetaboliteformationinchlamydomonasreinhardtiia13cnmrstudy