Esquinas-Ariza, Rosa M and Villar, Irene and Minguillón, Samuel and Zamarreño, Ángel and Reeder, Brandon J and et al (2025) Structural and functional comparison of hemoglobin Glb2-1 of Lotus japonicus with Glb1-1 and leghemoglobins. Journal of Experimental Botany, 77 (2). pp. 511-527. DOI https://doi.org/10.1093/jxb/eraf434
Esquinas-Ariza, Rosa M and Villar, Irene and Minguillón, Samuel and Zamarreño, Ángel and Reeder, Brandon J and et al (2025) Structural and functional comparison of hemoglobin Glb2-1 of Lotus japonicus with Glb1-1 and leghemoglobins. Journal of Experimental Botany, 77 (2). pp. 511-527. DOI https://doi.org/10.1093/jxb/eraf434
Esquinas-Ariza, Rosa M and Villar, Irene and Minguillón, Samuel and Zamarreño, Ángel and Reeder, Brandon J and et al (2025) Structural and functional comparison of hemoglobin Glb2-1 of Lotus japonicus with Glb1-1 and leghemoglobins. Journal of Experimental Botany, 77 (2). pp. 511-527. DOI https://doi.org/10.1093/jxb/eraf434
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.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Hemoglobins; Leghemoglobin; Lotus; Plant Proteins; Heme coordination; legume-rhizobium symbiosis; Lotus japonicus; phytohormones; pipecolic acid; plant hemoglobins; protein structure |
| Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
| SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
| Depositing User: | Unnamed user with email elements@essex.ac.uk |
| Date Deposited: | 21 Aug 2026 13:57 |
| Last Modified: | 21 Aug 2026 13:57 |
| URI: | http://repository.essex.ac.uk/id/eprint/42551 |
Available files
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