Abstract

Polyamines play an important role in plant growth and development, and response to abiotic stresses. Previously, differentially expressed proteins in sugar beet M14 (BvM14) under salt stress were identified by iTRAQ-based quantitative proteomics. One of the proteins was an S-adenosylmethionine decarboxylase (SAMDC), a key rate-limiting enzyme involved in the biosynthesis of polyamines. In this study, the BvM14-SAMDC gene was cloned from the sugar beet M14. The full-length BvM14-SAMDC was 1960 bp, and its ORF contained 1119 bp encoding the SAMDC of 372 amino acids. In addition, we expressed the coding sequence of BvM14-SAMDC in Escherichia coli and purified the ~40 kD BvM14-SAMDC with high enzymatic activity. Quantitative real-time PCR analysis revealed that the BvM14-SAMDC was up-regulated in the BvM14 roots and leaves under salt stress. To investigate the functions of the BvM14-SAMDC, it was constitutively expressed in Arabidopsis thaliana. The transgenic plants exhibited greater salt stress tolerance, as evidenced by longer root length and higher fresh weight and chlorophyll content than wild type (WT) under salt treatment. The levels of spermidine (Spd) and spermin (Spm) concentrations were increased in the transgenic plants as compared with the WT. Furthermore, the overexpression plants showed higher activities of antioxidant enzymes and decreased cell membrane damage. Compared with WT, they also had low expression levels of RbohD and RbohF, which are involved in reactive oxygen species (ROS) production. Together, these results suggest that the BvM14-SAMDC mediated biosynthesis of Spm and Spd contributes to plant salt stress tolerance through enhancing antioxidant enzymes and decreasing ROS generation.

Highlights

  • IntroductionPlant growth and development was frequently affected by adverse environment factors (e.g., cold, salt, alkali and drought), and salt stress is a major factor limiting crop production [1]

  • Plant growth and development was frequently affected by adverse environment factors, and salt stress is a major factor limiting crop production [1]

  • Through spermidine synthase and spermine synthase, Put is converted to Spm and Spd with decarboxylated S-adenosylmethionine as a donor [10,11]. dcSAM is synthesized from the decarboxylation of S-adenosylmethionine (SAM) in a reaction catalyzed by SAM decarboxylase (SAMDC) [12]

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Summary

Introduction

Plant growth and development was frequently affected by adverse environment factors (e.g., cold, salt, alkali and drought), and salt stress is a major factor limiting crop production [1]. When plants are exposed to salinity environment, the processes of protein synthesis and photosynthesis can be inhibited by excessive accumulation of salt in plants [2]. Under salt stress conditions, excessive reactive oxygen species (ROS) were accumulated in the plant, and high levels of ROS can cause membrane lipid peroxidation and metabolic perturbation [3]. Putrescine (Put), spermine (Spm) and spermidine (Spd) are the main types of polyamines. Through spermidine synthase and spermine synthase, Put is converted to Spm and Spd with decarboxylated S-adenosylmethionine (dcSAM) as a donor [10,11]. DcSAM is synthesized from the decarboxylation of S-adenosylmethionine (SAM) in a reaction catalyzed by SAM decarboxylase (SAMDC) [12] Through spermidine synthase and spermine synthase, Put is converted to Spm and Spd with decarboxylated S-adenosylmethionine (dcSAM) as a donor [10,11]. dcSAM is synthesized from the decarboxylation of S-adenosylmethionine (SAM) in a reaction catalyzed by SAM decarboxylase (SAMDC) [12]

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