Roles of acyl carrier proteins in ladderane fatty acid producing-organisms.

Chang Ding, Sabine Zimmermann, Lorenz Adrian, Tamara Schmidt, Tadeo Moreno-Chicano, Paola Granatino, Jolanta Nickel, Andreas Dietl, Thomas Barends

Journal: Biochimica et biophysica acta. General subjects 2025;1869(3):130763

PMID: 39805373

Abstract

Ladderanes are highly strained hydrocarbons consisting of two or more linearly concatenated cyclobutane rings. Strikingly, ladderane moieties are part of unique fatty acids and fatty alcohols that are exclusively found in the membrane lipids of anaerobic ammonium-oxidizing (anammox) bacteria. These bacteria express a distinctive gene cluster (cluster I) that has been suggested to be responsible for ladderane fatty acid (FA) biosynthesis in addition to a cluster likely involved in canonical FA biosynthesis (cluster III). In the anammox organism Kuenenia stuttgartiensis, cluster I encodes a unique acyl carrier protein (amxACP), whereas the ACP encoded by cluster III (KsACPII) was suggested to be involved in the production of canonical fatty acids. Here we present targeted isotope labeling studies using C-malonyl-ACPs to distinguish the roles of these ACPs. While in-vitroC incorporation into ladderane FAs was not observed, we show that KsACPII indeed functions in palmitate biosynthesis in the anammox organism Kuenenia stuttgartiensis. We present an experimental framework for continuing studies into fatty acid biosynthesis in anammox- and similar organisms.

Copyright © 2025 The Authors. Published by Elsevier B.V. All rights reserved.

Address: Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Jahnstrasse 29, D-69120 Heidelberg, Germany.; Molecular Environmental Biotechnology, Helmholtz Centre for Environmental Research - UFZ, Permoserstrasse 15, D-04318, Leipzig, Germany.; Molecular Environmental Biotechnology, Helmholtz Centre for Environmental Research - UFZ, Permoserstrasse 15, D-04318, Leipzig, Germany; Chair of Geobiotechnology, Technische Universität Berlin, Ackerstraße 76, D-13355 Berlin, Germany.; Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Jahnstrasse 29, D-69120 Heidelberg, Germany. Electronic address: [email protected].; Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Jahnstrasse 29, D-69120 Heidelberg, Germany. Electronic address: [email protected].
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