Genetic and lipidomic analyses suggest that Nostoc punctiforme, a plant-symbiotic cyanobacterium, does not produce sphingolipids

Author:

Belton Samuel12ORCID,Lamari Nadia341,Jermiin Lars S.541ORCID,Mariscal Vicente6ORCID,Flores Enrique6ORCID,McCabe Paul F.471ORCID,Ng Carl K. Y.417ORCID

Affiliation:

1. UCD School of Biology and Environmental Science, University College Dublin, Belfield, Dublin D4, Ireland

2. Present address: DBN Plant Molecular Biology Lab, National Botanic Gardens of Ireland, Dublin, Ireland

3. Present address: Philip Morris International, Quai Jeanrenaud 3, 2000, Neuchâtel, Switzerland

4. UCD Earth Institute, O’Brien Centre for Science, University College Dublin, Belfield, Dublin D4, Ireland

5. Research School of Biology, Australian National University, Canberra, ACT 2600, Australia

6. Instituto de Bioquímica Vegetal y Fotosíntesis, Consejo Superior de Investigaciones Científicas and Universidad de Sevilla, cicCartuja, Avda. Américo Vespucio 49, 41092 Seville, Spain

7. UCD Centre for Plant Science, University College Dublin, Belfield, Dublin D4, Ireland

Abstract

Sphingolipids, a class of amino-alcohol-based lipids, are well characterized in eukaryotes and in some anaerobic bacteria. However, the only sphingolipids so far identified in cyanobacteria are two ceramides (i.e., an acetylsphingomyelin and a cerebroside), both based on unbranched, long-chain base (LCB) sphingolipids in Scytonema julianum and Moorea producens , respectively. The first step in de novo sphingolipid biosynthesis is the condensation of l-serine with palmitoyl-CoA to produce 3-keto-diyhydrosphingosine (KDS). This reaction is catalyzed by serine palmitoyltransferase (SPT), which belongs to a small family of pyridoxal phosphate-dependent α-oxoamine synthase (AOS) enzymes. Based on sequence similarity to molecularly characterized bacterial SPT peptides, we identified a putative SPT (Npun_R3567) from the model nitrogen-fixing, plant-symbiotic cyanobacterium, Nostoc punctiforme strain PCC 73102 (ATCC 29133). Gene expression analysis revealed that Npun_R3567 is induced during late-stage diazotrophic growth in N. punctiforme . However, Npun_R3567 could not produce the SPT reaction product, 3-keto-diyhydrosphingosine (KDS), when heterologously expressed in Escherichia coli . This agreed with a sphingolipidomic analysis of N. punctiforme cells, which revealed that no LCBs or ceramides were present. To gain a better understanding of Npun_R3567, we inferred the phylogenetic position of Npun_R3567 relative to other bacterial AOS peptides. Rather than clustering with other bacterial SPTs, Npun_R3567 and the other cyanobacterial BioF homologues formed a separate, monophyletic group. Given that N. punctiforme does not appear to possess any other gene encoding an AOS enzyme, it is altogether unlikely that N. punctiforme is capable of synthesizing sphingolipids. In the context of cross-kingdom symbiosis signalling in which sphingolipids are emerging as important regulators, it appears unlikely that sphingolipids from N. punctiforme play a regulatory role during its symbiotic association with plants.

Funder

Irish Research Council

European Molecular Biology Organization

Publisher

Microbiology Society

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