# Molecular identification and functional analysis of HrpZ2, a new member of the harpin superfamily from Pseudomonas syringae, inducing hypersensitive response in tobacco

**Authors:** Kishori Lal, Anurag Joshi, Vartika Saini, Mujahid Mohammed, Pullabhotla V. S. R. N Sarma, Debashish Dey

PMC · DOI: 10.3389/fpls.2025.1665817 · 2026-01-15

## TL;DR

This paper identifies a new harpin protein from Pseudomonas syringae that triggers plant defense responses in non-host plants.

## Contribution

The study reports a new harpin gene (hrpZ2) and its functional role in inducing hypersensitive response in plants.

## Key findings

- HrpZ2 is a new member of the harpin superfamily with a predicted extracellular localization.
- HrpZ2 induces hypersensitive response in tobacco and other non-host plants through oxidative burst and defense enzyme activation.
- A 3D model of HrpZ2 was built and validated, revealing structural features like α-helices and disordered regions.

## Abstract

Harpins belong to a group of proteins with distinctive features such as heat stability, glycine richness, and absence of cysteine and are secreted by many Gram-negative phytopathogens via the type III secretion system. Harpins are known to trigger hypersensitive response followed by induction of systemic acquired resistance in non-host plants. However, the molecular mechanism of harpin-induced hypersensitive response remained largely unexplored, mainly because of the lack of structural information. In this study, we report the cloning of a new harpin gene (hrpZ2) from the Pseudomonas syringae strain MTCC-11950, belonging to the harpin superfamily. In silico analysis revealed that approximately 50.29% of the protein consists of α-helices, 48.53% are random coils, and only 1.16% are β-sheets, and nearly half (42%) of the protein consists of intrinsically disordered regions. Based on a prokaryotic predictive model and the presence of a signal peptide on its N-terminus, the subcellular localization of harpin is predicted as extracellular. To date, no experimentally determined crystal structure of any harpin protein is available. Therefore, we built and validated a three-dimensional model (with 99% of residues in allowed/additionally allowed regions and a Z-score of −5.3) of harpin. Phylogenetic analysis and functional domain studies revealed that this new harpin belongs to the harpin superfamily. Infiltration of harpin in tobacco leaves resulted in a hypersensitive response, which was associated with oxidative burst, callose deposition, localized cell death, and increased activity of defense-related enzymes such as phenylalanine ammonia-lyase and polyphenol oxidase. Furthermore, infiltration of harpin in non-host plants from different angiosperm families induced a hypersensitive response, indicating broad-spectrum agricultural applicability of this new harpin protein. This study elucidates the molecular and functional properties of the new harpin protein and its ability to induce hypersensitive response across a broad range of non-host plants.

## Linked entities

- **Species:** Pseudomonas syringae (taxon 317)

## Full-text entities

- **Genes:** phenylalanine ammonia-lyase [NCBI Gene 107786762]
- **Chemicals:** cysteine (MESH:D003545)
- **Species:** Pseudomonas syringae (species) [taxon 317], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12854069/full.md

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Source: https://tomesphere.com/paper/PMC12854069