# Structural and functional comparison of hemoglobin Glb2-1 of Lotus japonicus with Glb1-1 and leghemoglobins

**Authors:** Rosa M Esquinas-Ariza, Irene Villar, Samuel Minguillón, Ángel Zamarreño, Carmen Pérez-Rontomé, Brandon J Reeder, Niels Sandal, Deng Yan, José M García-Mina, Deqiang Duanmu, Marta Martínez-Júlvez, Manuel Becana

PMC · DOI: 10.1093/jxb/eraf434 · Journal of Experimental Botany · 2025-09-30

## TL;DR

This study compares the structure and function of hemoglobins in Lotus japonicus, revealing distinct roles for Glb1-1 and Glb2-1 in plant immunity and reproduction.

## Contribution

The paper identifies key residues in Glb2-1 critical for oxygen binding and reveals distinct functional roles for Glb1-1 and Glb2-1.

## Key findings

- Glb2-1 is primarily found in nodules and has a distinct function from leghemoglobins.
- Glb1-1 is involved in plant defense, as shown by increased salicylic acid and pipecolic acid in its mutant.
- Glb2-1 plays a role in the reproductive stage, indicated by reduced jasmonoyl-isoleucine levels in its mutant.

## Abstract

The legume Lotus japonicus expresses nine hemoglobins, including leghemoglobins (Lbs), class 1 phytoglobin (Glb1-1), and an unusual phytoglobin (Glb2-1). Quantitative PCR, proteomics, and plant mutant analyses indicated that Glb2-1 is mainly present in nodules without replacing Lb function, but is also in roots and photosynthetic tissues. Comparison of hormonal profiles of the knock-out mutants glb1-1, glb2-1, and glb1-1/2-1 showed that Glb1-1 and Glb2-1 have distinct functions. The increase of salicylic acid in the leaves of glb1-1 revealed a role of Glb1-1 in the defense response, which was corroborated by accumulation of pipecolic acid, a metabolite involved in plant immunity. In contrast, the decrease of bioactive jasmonoyl-isoleucine in glb2-1 was consistent with a role of Glb2-1 in the plant's reproductive stage. The mutants also showed changes in cytokinins, gibberellins, and polyamines, but without clear distinctive patterns. The crystal structure of Glb2-1 was determined to 1.6 Å resolution and compared with those of soybean Lba and Arabidopsis Glb1. In combination with mutant versions of Glb2-1, residues Tyr31, His64, and Cys65 were identified as critical for O2-binding stability. Spectral changes in heme coordination when Tyr31 is substituted for Phe highlights the importance of the residue at the B10 position for Lb and Glb function.

## Linked entities

- **Genes:** glb-11 (GLoBin related) [NCBI Gene 175516], glb-21 (Globin domain-containing protein) [NCBI Gene 3565100]
- **Proteins:** glb-11 (GLoBin related), glb-21 (Globin domain-containing protein), LRBA (LPS responsive beige-like anchor protein)
- **Chemicals:** salicylic acid (PubChem CID 338), pipecolic acid (PubChem CID 849), gibberellins (PubChem CID 522636)
- **Species:** Lotus japonicus (taxon 34305), Arabidopsis (taxon 3701)

## Full-text entities

- **Chemicals:** gibberellins (MESH:D005875), salicylic acid (MESH:D020156), heme (MESH:D006418), pipecolic acid (MESH:C031345), jasmonoyl-isoleucine (MESH:C532883), O2- (-), cytokinins (MESH:D003583), polyamines (MESH:D011073)
- **Species:** Lotus japonicus (species) [taxon 34305], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702]
- **Mutations:** Tyr31 is substituted for Phe

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12794238/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12794238/full.md

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Source: https://tomesphere.com/paper/PMC12794238