Structural basis and evolutionary pathways of glycerol-1-phosphate transport in marine bacteria

N Ning Wang L Linda M. Westermann (School of Life Sciences, University of Warwick) M Mingyu Li C Chun-Yang Li (MOE Key Laboratory of Evolution and Marine Biodiversity, State Key Laboratory of Marine Food Processing and Safety Control, College of Marine Life Sciences & Frontiers Science Center for Deep Ocean Multispheres and Earth System, Ocean University of China) A Andrew R. J. Murphy (School of Life Sciences, University of Warwick) Z Zengtian Gu (State Key Laboratory of Microbial Technology, Marine Biotechnology Research Center, Shandong University) E Eleonora Silvano (School of Life Sciences, University of Warwick) C Claudia A. Blindauer (Department of Chemistry, University of Warwick) I Ian D. E. A. Lidbury (Molecular Microbiology: Biochemistry to Disease, School of Biosciences, University of Sheffield) Y Yu-Zhong Zhang D David J. Scanlan (School of Life Sciences, University of Warwick) Y Yin Chen (School of Biosciences, University of Birmingham)

Abstract

All cells use lipid membranes to maintain cellular integrity and function, though Archaea utilize lipids composed of glycerol-1-phosphate (G1P), while Bacteria and Eukaryotes use glycerol-3-phosphate (G3P). Given that Archaea contribute significantly to global marine biomass, accounting for 0.3 gigatonnes (Gt) of carbon in the oceans, we aimed to uncover how archaeal G1P is recycled by marine microorganisms. Through a multidisciplinary approach combining microbiology, biochemistry, and structural biology, we identified a G1P transporter in marine bacteria, which we named GpxB. Phylogenetic analysis revealed that GpxB belongs to the organic phosphonate transporter (PhnT) family and is widely distributed in the marine microbiome, found in approximately 5 to 10% of microbial cells in surface marine waters. Strikingly, we also identified a second G1P transporter, UgpB, that is known to transport G3P and belongs to the carbohydrate uptake transporter-1 (CUT1) family, in the model bacterium Phaeobacter sp. MED193. To explore the evolutionary pathways that led to the formation of G1P binding sites in both the PhnT and CUT1 families, we determined the structures of GpxB and UgpB bound to G1P and G3P. Using structure-guided mutagenesis and a comparative analysis of the binding pockets within the PhnT and CUT1 families, we traced their evolutionary trajectories, highlighting the distinct strategies through which G1P-binding sites developed in these two protein families.

Article Details

Volume / Issue Vol. 122, Issue 50
Published December 16, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (12)

N

Ning Wang

L

Linda M. Westermann

School of Life Sciences, University of Warwick

M

Mingyu Li

C

Chun-Yang Li

MOE Key Laboratory of Evolution and Marine Biodiversity, State Key Laboratory of Marine Food Processing and Safety Control, College of Marine Life Sciences & Frontiers Science Center for Deep Ocean Multispheres and Earth System, Ocean University of China

A

Andrew R. J. Murphy

School of Life Sciences, University of Warwick

Z

Zengtian Gu

State Key Laboratory of Microbial Technology, Marine Biotechnology Research Center, Shandong University

E

Eleonora Silvano

School of Life Sciences, University of Warwick

C

Claudia A. Blindauer

Department of Chemistry, University of Warwick

I

Ian D. E. A. Lidbury

Molecular Microbiology: Biochemistry to Disease, School of Biosciences, University of Sheffield

Y

Yu-Zhong Zhang

D

David J. Scanlan

School of Life Sciences, University of Warwick

Y

Yin Chen

School of Biosciences, University of Birmingham