Cargando…

A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate

The Calvin–Benson cycle (CB cycle) is quantitatively the most important metabolic pathway for CO(2) fixation. In the canonical CB cycle, fructose 6-phosphate (F6P), fructose 1,6-bisphosphate (FBP), sedoheptulose 7-phosphate (S7P), and sedoheptulose 1,7-bisphosphate (SBP) appear as essential intermed...

Descripción completa

Detalles Bibliográficos
Autor principal: Ohta, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927339/
https://www.ncbi.nlm.nih.gov/pubmed/35296702
http://dx.doi.org/10.1038/s41598-022-07836-7
_version_ 1784670425118146560
author Ohta, Jun
author_facet Ohta, Jun
author_sort Ohta, Jun
collection PubMed
description The Calvin–Benson cycle (CB cycle) is quantitatively the most important metabolic pathway for CO(2) fixation. In the canonical CB cycle, fructose 6-phosphate (F6P), fructose 1,6-bisphosphate (FBP), sedoheptulose 7-phosphate (S7P), and sedoheptulose 1,7-bisphosphate (SBP) appear as essential intermediates, where F6P is formed from FBP by the fructose 1,6-bisphosphatase (FBPase) reaction, and S7P is formed from SBP by the sedoheptulose 1,7-bisphosphatase (SBPase) reaction. Although the involvement of SBP and SBPase in the canonical CB cycle is consistent with the reported dependency of photosynthetic carbon metabolism on SBPase, the involvement of FBP and FBPase is not completely consistent with the reported FBP- or FBPase-related findings such as, although with a diminished growth rate, an Arabidopsis mutant lacking FBPase grew photoautotrophically in soil. Here, we show a novel variant of the CB cycle involving SBP, SBPase, and transaldolase, but neither FBP nor FBPase. This novel variant, named the S7P-removing transaldolase variant, bypasses FBP. This variant explains the FBP- or FBPase-related findings more easily than the canonical CB cycle as well as the dependency of photosynthetic carbon metabolism on SBPase and further suggests that co-overexpression of SBPase and transaldolase can be a strategy for enhancing photosynthetic carbon metabolism, which is important for the global environment.
format Online
Article
Text
id pubmed-8927339
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-89273392022-03-17 A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate Ohta, Jun Sci Rep Article The Calvin–Benson cycle (CB cycle) is quantitatively the most important metabolic pathway for CO(2) fixation. In the canonical CB cycle, fructose 6-phosphate (F6P), fructose 1,6-bisphosphate (FBP), sedoheptulose 7-phosphate (S7P), and sedoheptulose 1,7-bisphosphate (SBP) appear as essential intermediates, where F6P is formed from FBP by the fructose 1,6-bisphosphatase (FBPase) reaction, and S7P is formed from SBP by the sedoheptulose 1,7-bisphosphatase (SBPase) reaction. Although the involvement of SBP and SBPase in the canonical CB cycle is consistent with the reported dependency of photosynthetic carbon metabolism on SBPase, the involvement of FBP and FBPase is not completely consistent with the reported FBP- or FBPase-related findings such as, although with a diminished growth rate, an Arabidopsis mutant lacking FBPase grew photoautotrophically in soil. Here, we show a novel variant of the CB cycle involving SBP, SBPase, and transaldolase, but neither FBP nor FBPase. This novel variant, named the S7P-removing transaldolase variant, bypasses FBP. This variant explains the FBP- or FBPase-related findings more easily than the canonical CB cycle as well as the dependency of photosynthetic carbon metabolism on SBPase and further suggests that co-overexpression of SBPase and transaldolase can be a strategy for enhancing photosynthetic carbon metabolism, which is important for the global environment. Nature Publishing Group UK 2022-03-16 /pmc/articles/PMC8927339/ /pubmed/35296702 http://dx.doi.org/10.1038/s41598-022-07836-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ohta, Jun
A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title_full A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title_fullStr A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title_full_unstemmed A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title_short A novel variant of the Calvin–Benson cycle bypassing fructose bisphosphate
title_sort novel variant of the calvin–benson cycle bypassing fructose bisphosphate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927339/
https://www.ncbi.nlm.nih.gov/pubmed/35296702
http://dx.doi.org/10.1038/s41598-022-07836-7
work_keys_str_mv AT ohtajun anovelvariantofthecalvinbensoncyclebypassingfructosebisphosphate
AT ohtajun novelvariantofthecalvinbensoncyclebypassingfructosebisphosphate