Characterization of a Pipecolic Acid Biosynthesis Pathway Required for Systemic Acquired Resistance. Issue 10 (6th October 2016)

• Record Type: Journal Article
• Authors: Ding, Pingtao; Rekhter, Dmitrij; Ding, Yuli; Feussner, Kirstin; Busta, Lucas; Haroth, Sven; Xu, Shaohua; Li, Xin; Jetter, Reinhard; Feussner, Ivo; Zhang, Yuelin
• Is Part Of: The Plant Cell. Volume 28:Issue 10(2016)
• Page Start: 2603
• Page End: 2615
• Publication Date: 2016-10-06
• DOI: 10.1105/tpc.16.00486
• Languages: English
• ISSNs: 1040-4651

Abstract

Abstract : SAR-DEFICIENT4 (SARD4) encodes a key enzyme for pipecolic acid (Pip) biosynthesis and is required for the establishment of systemic acquired resistance to pathogen infection in Arabidopsis. Abstract: Systemic acquired resistance (SAR) is an immune response induced in the distal parts of plants following defense activation in local tissue. Pipecolic acid (Pip) accumulation orchestrates SAR and local resistance responses. Here, we report the identification and characterization of SAR-DEFICIENT4 ( SARD4 ), which encodes a critical enzyme for Pip biosynthesis in Arabidopsis thaliana . Loss of function of SARD4 leads to reduced Pip levels and accumulation of a Pip precursor, Δ 1 -piperideine-2-carboxylic acid (P2C). In Escherichia coli, expression of the aminotransferase ALD1 leads to production of P2C and addition of SARD4 results in Pip production, suggesting that a Pip biosynthesis pathway can be reconstituted in bacteria by coexpression of ALD1 and SARD4. In vitro experiments showed that ALD1 can use l -lysine as a substrate to produce P2C and P2C is converted to Pip by SARD4. Analysis of sard4 mutant plants showed that SARD4 is required for SAR as well as enhanced pathogen resistance conditioned by overexpression of the SAR regulator FLAVIN-DEPENDENT MONOOXYGENASE1. Compared with the wild type, pathogen-induced Pip accumulation is only modestly reduced in the local tissue of sard4 mutant plants, but it is below detection in distal leaves, suggesting that Pip is synthesized in systemic tissue by SARD4-mediated reduction of P2C and biosynthesis of Pip in systemic tissue contributes to SAR establishment.