Glycolytic Shunts Replenish the Calvin-Benson-Bassham Cycle as Anaplerotic Reactions in Cyanobacteria.

Calvin–Benson–Bassham cycle Embden–Meyerhof–Parnas pathway Entner–Doudoroff pathway central carbohydrate metabolism cyanobacteria oxidative pentose phosphate pathway

Journal

Molecular plant
ISSN: 1752-9867
Titre abrégé: Mol Plant
Pays: England
ID NLM: 101465514

Informations de publication

Date de publication:
02 03 2020
Historique:
received: 02 08 2019
revised: 16 12 2019
accepted: 10 01 2020
pubmed: 12 2 2020
medline: 24 11 2020
entrez: 12 2 2020
Statut: ppublish

Résumé

The recent discovery of the Entner-Doudoroff (ED) pathway as a third glycolytic route beside Embden-Meyerhof-Parnas (EMP) and oxidative pentose phosphate (OPP) pathway in oxygenic photoautotrophs requires a revision of their central carbohydrate metabolism. In this study, unexpectedly, we observed that deletion of the ED pathway alone, and even more pronounced in combination with other glycolytic routes, diminished photoautotrophic growth in continuous light in the cyanobacterium Synechocystis sp. PCC 6803. Furthermore, we found that the ED pathway is required for optimal glycogen catabolism in parallel to an operating Calvin-Benson-Bassham (CBB) cycle. It is counter-intuitive that glycolytic routes, which are a reverse to the CBB cycle and do not provide any additional biosynthetic intermediates, are important under photoautotrophic conditions. However, observations on the ability to reactivate an arrested CBB cycle revealed that they form glycolytic shunts that tap the cellular carbohydrate reservoir to replenish the cycle. Taken together, our results suggest that the classical view of the CBB cycle as an autocatalytic, completely autonomous cycle that exclusively relies on its own enzymes and CO2 fixation to regenerate ribulose-1,5-bisphosphate for Rubisco is an oversimplification. We propose that in common with other known autocatalytic cycles, the CBB cycle likewise relies on anaplerotic reactions to compensate for the depletion of intermediates, particularly in transition states and under fluctuating light conditions that are common in nature.

Identifiants

pubmed: 32044444
pii: S1674-2052(20)30032-0
doi: 10.1016/j.molp.2020.02.002
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

471-482

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Alexander Makowka (A)

Department of Biology, Botanical Institute, University Kiel, 24118 Kiel, Germany.

Lars Nichelmann (L)

Department of Biology, Botanical Institute, University Kiel, 24118 Kiel, Germany.

Dennis Schulze (D)

Institute for Systems Biotechnology, Saarland University, 66123 Saarbrücken, Germany.

Katharina Spengler (K)

Department of Biology, Botanical Institute, University Kiel, 24118 Kiel, Germany.

Christoph Wittmann (C)

Institute for Systems Biotechnology, Saarland University, 66123 Saarbrücken, Germany.

Karl Forchhammer (K)

Organismic Interactions Department, Interfaculty Institute for Microbiology and Infection Medicine, University Tübingen, 72076 Tübingen, Germany.

Kirstin Gutekunst (K)

Department of Biology, Botanical Institute, University Kiel, 24118 Kiel, Germany. Electronic address: kgutekunst@bot.uni-kiel.de.

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Classifications MeSH