Overexpressing the N‐terminus of CATALASE2 enhances plant jasmonic acid biosynthesis and resistance to necrotrophic pathogen Botrytis cinerea B05.10

Abstract Salicylic acid (SA) acts antagonistically to jasmonic acid (JA) in plant immunity. We previously reported that CATALASE2 (CAT2) promotes JA‐biosynthetic acyl‐CoA oxidase (ACX) activity to enhance plant resistance to necrotrophic Botrytis cinerea, and SA represses JA biosynthesis through inhibiting CAT2 activity, while the underlying mechanism remains to be further elucidated. Here, we report that the truncated CAT2 N‐terminus (CAT2‐N) interacts with and promotes ACX2/3, and CAT2‐N‐overexpressing plants have increased JA accumulation and enhanced resistance to B. cinerea B05.10, but compromised antagonism of SA on JA. Catalase inhibitor treatment or mutating CAT2 active amino acids abolished CAT2 H2O2‐decomposing activity but did not affect its promotion of ACX2/3 activity via interaction. CAT2‐N, a truncated protein with no catalase activity, interacted with and promoted ACX2/3. Overexpressing CAT2‐N in Arabidopsis plants resulted in increased ACX activity, higher JA accumulation, and stronger resistance to B. cinerea B05.10 infection. Additionally, SA dramatically repressed JA biosynthesis and resistance to B. cinerea in the wild type but not in the CAT2‐N‐overexpressing plants. Together, our study reveals that CAT2‐N can be utilized as an accelerator for JA biosynthesis during plant resistance to B. cinerea B05.10, and this truncated protein partly relieves SA repression of JA biosynthesis in plant defence responses.

. Based on lifestyles, plant pathogens can be generally categorized into biotrophic and necrotrophic pathogens, which derive nutrients mainly from living host tissues or dead/dying cells, respectively (Qi et al., 2012;Spoel & Dong, 2008).
Therefore, accurate activation of a defence strategy is the prerequisite for successful plant resistance in response to distinct pathogens with different lifestyles (Adedeji & Babalola, 2020;Ochoa-Lopez et al., 2020;Zhang et al., 2020b).
Phytohormones play essential roles in plant resistance against pathogen infection through regulating the expression of a battery of genes related to pathogen recognition and defence response (Koornneef & Pieterse, 2008;Lopez et al., 2008). It has been widely documented that salicylic acid (SA) plays an essential role in plant resistance to biotrophic and semibiotrophic pathogens such as the model pathogen Pseudomonas syringae pv. tomato DC3000 (Pst DC3000) (Chen et al., 2020a;Peng et al., 2021;Zhang et al., 2020c).
On infection with Pst DC3000, SA accumulation is rapidly induced in plants by the activation of SA biosynthesis and repression of SA metabolism, resulting in translocation of NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (NPR1) from cytoplasm to nucleus. NPR1, as a master transcription regulator in the plant immune response, interacts with other transcription factors in the nucleus and modulates the expression of a large number of defence-related genes, including multiple pathogenesis-related (PR) genes (Budimir et al., 2021;Liu et al., 2020d;Spoel & Dong, 2008;Zavaliev et al., 2020). In addition, SA can also directly bind to and inhibit catalase (CAT), a key enzyme catalysing the degradation of H 2 O 2 , thus increasing H 2 O 2 accumulation in plant cells (Chen et al., 1993b;Sanchez-Casas & Klessig, 1994). High levels of H 2 O 2 enhance plant pathogen resistance through directly killing the invasive pathogens as an oxidative antimicrobial chemical, strengthening the cell wall barrier as a cross-linker for structural proteins, and also upregulating the expression of some defence-related genes as a signalling molecule, thus serving as an important factor involved in SA-mediated plant resistance to biotrophic pathogens (Bradley et al., 1992;Chen et al., 2020b;Jasso-Robles et al., 2020;Shen et al., 2021;Su et al., 2018a;Zhao et al., 2021). Previous reports documented a vital role of CAT in the plant immune response. For example, repression of CAT expression in tobacco or mutation of CAT2 in Arabidopsis results in enhanced resistance to bacterial pathogens with decreased catalase activity and increased H 2 O 2 accumulation, while overexpressing CAT1 dampens pathogen-induced H 2 O 2 accumulation and the defence response in tobacco (Chaouch et al., 2010;Mittler et al., 1999;Yuan et al., 2017).
Although it is reported that SA elicits an antagonistic effect on JA in plant immune responses (Ndamukong et al., 2007;Spoel et al., 2003), SA also plays a role in plant resistance to B. cinerea. For example, repressing SA accumulation in Arabidopsis plants, by expressing bacterial nahG that encodes an SA hydroxylase or by applying a phenylalanine ammonia-lyase inhibitor, significantly increases susceptibility to both Pst DC3000 and B. cinerea infection (Ferrari et al., 2003), revealing that both SA and JA are crucial phytohormones mediating plant defence responses to biotrophic and necrotrophic pathogens.
We previously reported that the acx2-1 acx3-6 mutant with mutation of both ACX2 and ACX3 has extremely low acyl-CoA oxidase activity with OPC4-CoA as the substrate; thus, the mutant exhibited increased susceptibility to B. cinerea due to a decreased JA level, revealing a key role of ACX2/3 in B. cinerea infection-induced JA biosynthesis . We also found that CAT2 interacts with ACX2/3 in peroxisomes and promotes their activity to enhance JA biosynthesis, increasing plant resistance to necrotrophic B. cinerea B05.10 infection Yuan et al., 2017). The Arabidopsis cat2-1 mutant has decreased ACX activity, repressed JA accumulation, and thus reduced resistance to B. cinerea B05.10 . However, the mechanism underlying CAT2-mediated promotion of ACX activity via their interaction remains elusive. Elucidating how CAT2 increases ACX activity would provide more insight into mechanism of the plant defence response.
Here, we report that the N-terminus, but not the C-terminus, of CAT2 interacts with and promotes ACX2/3, and overexpressing the CAT2-N terminus enhances plant ACX activity, JA biosynthesis, and thus resistance to B. cinerea B05.10 infection. Our study showed that treatment of catalase inhibitor 3-amino-1,2,4-triazole (3-AT) or mutating CAT2 active amino acid sites necessary for catalase activity severely abolished CAT2 H 2 O 2 -decomposing activity but did not affect CAT2 interaction with ACX2/3 and promotion on their ACX activity. The truncated N-terminus of CAT2 (CAT2-N) had no catalase activity but can also interact with and promote ACX2/3. Furthermore, we overexpressed CAT2-N fused with type I peroxisomal targeting signal (PTS1) in wildtype Arabidopsis plants, and found that the transgenic 35S::CAT2-N-PTS1 plants had increased ACX activity, JA accumulation, and showed enhanced resistance to B. cinerea B05.10 infection. In addition, the transgenic plants showed diminished antagonism of SA on JA biosynthesis. Together, our study reveals that CAT2-N interacts with and promotes ACX2/3 implicated in JA biosynthesis and enhances plant resistance to B. cinerea, and this truncated protein partly relieves SA repression of JA biosynthesis in plant defence responses.

| CAT2 promotes ACX2/3 activity through interaction as well as catalase activity
Previously, we reported that CAT2 interacts with and promotes ACX2/3 to enhance JA biosynthesis, thus increasing plant resistance to necrotrophic B. cinerea B05.10 infection , while how CAT2 increases ACX activity is not clear. We previously speculated that CAT2 may promote ACX activity by scavenging H 2 O 2 , one of the products of ACX with fatty acyl-CoA as the substrate. Indeed, inhibition of CAT2 activity by SA, a catalase inhibitor, significantly represses CAT2-mediated stimulation of ACX2/3 activity. However, we also found that even high concentrations of SA treatment cannot totally diminish the stimulatory effect of CAT2 on ACX2/3 activity, suggesting a possibility that CAT2 may also promote ACX2/3 activity through its interaction in addition to its H 2 O 2 -decomposing activity.
To investigate this, we expressed and purified ACX2 and ACX3 proteins in Escherichia coli, and assayed their ACX activity with OPC4-CoA in the presence or absence of purified CAT2 protein according to our previously reported method . Our results showed that the activity of ACX2 or ACX3 was significantly increased when CAT2 was added (Figure 1a), which is consistent with our previous report . In addition, 3-amino-1,2,4-triazole (3-AT), a widely used strong inhibitor of catalase (Liu et al., 2020b), was used, and we found that 3-AT dramatically suppressed CAT2 but not ACX2 or ACX3 activity, while 3-AT markedly repressed CAT2 stimulation of ACX2/3 activity (Figure 1a,b), suggesting that the H 2 O 2 -decomposing activity of CAT2 functions in promotion of ACX2/3 activity. However, we also found that when CAT2 activity was inhibited to a nearly undetectable level by high concentrations of 3-AT, ACX2 or ACX3 activity was still significantly higher in the presence of CAT2 than in the absence of CAT2 (Figure 1a,b), suggesting that CAT2 may promote ACX2/3 activity through its interaction as well as catalase activity.
To confirm this, total proteins from the wildtype plant and cat2-1, a T-DNA insertion mutant of CAT2, were extracted to examine their ACX activity. Our results showed that 3-AT inhibited both catalase activity and ACX activity in the wildtype plants in a dosage-dependent manner, while 10 mM 3-AT-treated wildtype plant proteins had similar low catalase activity but still higher ACX activity compared with proteins from the cat2-1 mutant (Figure 1c,d), further supporting that CAT2 promotes ACX2/3 activity through its interaction.
Together, these results clearly show that CAT2 promotes ACX2/3 activity at least partially through the interaction.

| The N-terminus of CAT2 interacts with and promotes ACX2 and ACX3
Protein-protein interaction generally occurs in a small protein interface. To investigate which fragment of CAT2 interacts with and promotes ACX2/3, we analysed Arabidopsis CAT2 protein structure according to its homolog protein structure (Poulos, 2010), and divided it into N-terminus (CAT2-N) and C-terminus (CAT2-C), which was further divided into H-fragment (heme ligand signature- in plants. However, we observed that the fluorescence in N. benthamiana leaves coexpressing cYFP-tagged ACX2 or ACX3 and nYFPtagged CAT2 was mainly in peroxisomes, while the fluorescence was mainly in the cytoplasm for cYFP-tagged ACX2 or ACX3 and nYFPtagged CAT2-N. This is perhaps due to the lack of a peroxisomal targeting signal (PTS) sequence in CAT2-N. Thus, we fused a type I PTS sequence, Ser-Lys-Leu (SKL) with nYFP-tagged CAT2-N, and assayed its interaction with ACX2 and ACX3 by BiFC. Our results showed that coexpressing nYFP-tagged CAT2-N-SKL and cYFP-tagged ACX2 or ACX3 resulted in significant fluorescence mainly in peroxisomes in N. benthamiana leaves (Figure 3c,d).
To determine whether the CAT2-N fragment has H 2 O 2decomposing activity, we expressed and purified CAT2-N in E. coli and examined its catalase activity. Our results showed that compared with the full-length CAT2 protein, CAT2-N exhibited no catalase activity (Figure 2a). This prompted us to further assay whether CAT2-N can promote the activity of ACX2 and ACX3 as they have interaction in vitro and in vivo. Therefore, we assessed the activity of ACX2 and ACX3 in the presence or absence of CAT2-N. Our results showed that the activity of ACX2 and ACX3 was significantly increased as CAT2-N protein was added ( Figure 3b). These data clearly indicate that the N-terminus of CAT2 interacts with ACX2/3 and promotes their activity.

| CAT2-N partially rescues increased susceptibility of cat2-1 mutant to B. cinerea B05.10
The stimulatory effect of CAT2-N on ACX2/3 activity in vitro suggests its possible in vivo role in plant resistance to B. cinerea B05.10.
We therefore generated CAT2::CAT2-N-SKL cat2-1 transgenic plants in which the expression of CAT2-N-SKL was driven by the CAT2 native promoter in the cat2-1 mutant, and then tested their resistance to B. cinerea B05.10. Our results showed that the cat2-1 mutant was susceptible to B. cinerea B05.10 compared with the wildtype plant, as we previously reported , while the expression of CAT2-N-SKL driven by the CAT2 promoter did not alter the catalase activity of the cat2-1 mutant but partially rescued the sensitivity of the mutant to infection (Figure 4a,b). Additionally, we examined the ACX activity and JA levels in these transgenic plants, and found that decreased ACX activity and JA level in the cat2-1 mutant were also partially increased by the expression of CAT2-N-SKL (Figure 4c,d).
Moreover, we detected the expression of PDF1.2, a JA-responsive marker gene involved in plant response to necrotrophic pathogen infection, in the wildtype, cat2-1, and these transgenic plants. As shown in Figure 4d, lower expression of PDF1.2 in B. cinerea-infected cat2-1 mutant was partly reverted by CAT2-N-SKL, which is consistent with the effect of CAT2-N-SKL on ACX activity and JA levels in the mutant. These data clearly indicate that CAT2-N can promote F I G U R E 1 Inhibiting CAT2 activity cannot completely diminish the stimulatory effect of CAT2 on ACX2/3 enzymatic activity. (a) The enzymatic activities of ACX2 and ACX3 were assessed with OPC4-CoA as the substrate. One microgram of ACX2 or ACX3 protein was added in the reaction buffer containing different concentrations of CAT2 and 3-AT, and the reaction was incubated at 25 °C for 30 min. As ACX2 and ACX3 convert substrate OPC4-CoA to product Δ 2 -OPC4-CoA, thus the ACX2 andACX3 activities are defined as the ratio of Δ 2 -OPC4-CoA to (Δ 2 -OPC4-CoA + OPC4-CoA). The method to detect ACX activity is shown in the Experimental Procedures section. The activity of untreated ACX2 or ACX3 was set to 1. (b) Catalase activity of purified CAT2 protein treated with different concentrations of 3-AT was assayed. The ACX activity (c) and catalase activity (d) of the untreated and 3-AT-treated proteins extracted from the 4-week-old wildtype and cat2-1 mutant plant were assayed. Data are means (± SD) of three biological replicates. Bars with different letters indicate significant differences at p < 0.05, revealed using a one-way analysis of variance with a Tukey's multiple comparison test. Asterisks indicate significant differences using Student's t test, *p < 0.05, **p < 0.01, ***p < 0.001 ACX2/3 activity in vivo to stimulate ACX2/3 activity and JA biosynthesis, thus partially rescuing reduced resistance of the cat2-1 mutant to B. cinerea B05.10.

| CAT2-N-overexpressing plants have enhanced resistance to B. cinerea B05.10
To further confirm the role of CAT2-N in plant ACX activity, JA biosynthesis, and resistance to B. cinerea B05.10, we generated trans- were assessed with OPC4-CoA as the substrate in the presence or absence of the WT, mutated, and N-terminal CAT2 proteins. One microgram of ACX2 or ACX3 protein was added in the reaction buffer with or without 1 µg of CAT2-H65A, CAT2-V106A, CAT2-F143V, CAT2-Y348V, or CAT2-N protein, and the reaction was incubated at 25 °C for 30 min, and then OPC4-CoA and Δ 2 -OPC4-CoA in the reaction buffer were measured. Data are means (± SD) of three biological replicates. Bars with different letters indicate significant differences at p < 0.05, revealed using a one-way analysis of variance with a Tukey's multiple comparison test act antagonistically in plant immune responses (Ndamukong et al., 2007;Spoel et al., 2003). Our previous report documented that

| D ISCUSS I ON
In this study, we identified CAT2-N, not CAT2-C, as an accelerator for JA biosynthesis during plant resistance to B. cinerea through interacting with and promoting ACX2/3. In addition, mutation of the crucial active amino acids of CAT2, including His65, Val106, Phe143, and Tyr348, resulted in extremely low catalase activity for H 2 O 2 degradation, while these mutated CAT2 proteins still interacted with ACX2 and ACX3, and stimulated their ACX activity ( Figure 2), further supporting that CAT2 promotes ACX activity at A recent report showed that a loss-of-function mutant of AtIQM1 (IQ-Motif Containing Protein1), iqm1-1, exhibited higher resistance to biotrophic Pst DC3000 but susceptibility to necrotrophic F I G U R E 4 The CAT2-N-SKL partially rescues decreased resistance of cat2-1 mutant to Botrytis cinerea B05.10. Photographs of rosette leaves (a) cut from 4-week-old wildtype (WT), cat2-1, and CAT2::CAT2-N-SKL cat2-1 transgenic plants at 3 days after infection with B. cinerea B05.10 spores. The relative lesion size is shown (b). Data are means (± SD) of three biological replicates. Bars with different letters indicate significant differences at p < 0.05, revealed using a one-way analysis of variance (ANOVA) with a Tukey's multiple comparison test. (c) Catalase activity of rosette leaves cut from 4-week-old WT, cat2-1, and CAT2::CAT2-N-SKL cat2-1 transgenic plants. Data are means (± SD) of three biological replicates. Bars with different letters indicate significant differences at p < 0.05, revealed using a one-way ANOVA with a Tukey's multiple comparison test. The ACX activity (c) and JA levels (d) in the WT, cat2-1, and CAT2::CAT2-N-SKL cat2-1 transgenic plants infected with or without B. cinerea B05.10. Data are means (± SD) of three biological replicates. Different letters indicate statistically significant differences by two-way ANOVA with Tukey's post hoc test (p < 0.05). (f) The expression of PDF1.2 was assayed by quantitative reverse transcription PCR in the leaves of the WT, cat2-1, and CAT2::CAT2-N-SKL cat2-1 transgenic plants 3 days after infection with B. cinerea B05.10. ACTIN2/8 was used as the reference gene. Data are means (± SD) of three biological replicates. Different letters indicate statistically significant differences by two-way ANOVA with Tukey's post hoc test (p < 0.05) B. cinerea B05.10 than the wildtype plant (Lv et al., 2019). AtIQM1 interacts with and promotes CAT2 activity, especially in the presence of calmodulin5 (CaM5) in Arabidopsis, increasing the activity of the JA biosynthetic enzymes ACX2 and ACX3 (Lv et al., 2019).
In this study, we found that overexpressing CAT2-N in the wildtype plants did not significantly alter plant resistance to Pst DC3000 but enhanced plant resistance to B. cinerea B05.10. It might be worth generating transgenic crops with increased CAT2-N expression but decreased IQM1 expression, as they may have higher resistance to both biotrophic Pst DC3000 and necrotrophic B. cinerea B05.10.
CAT2 is synthesized in the cytoplasm and imported into peroxisomes based on its C-terminal atypical PTS1, Q480-K481-L482 (Fujikawa et al., 2019). The truncated N-terminus of CAT2 cannot be properly localized in peroxisomes due to a lack of PTS, thus the interaction between CAT2 and ACX2/3 was in the cytoplasm, as shown in our results (Figure 3c,d). Even though CAT2-N can promote ACX2/3 activity in vitro, we speculated that CAT2-N without a PTS sequence fails to stimulate ACX activity in planta because ACX2 and ACX3 are peroxisome-localized proteins and their substrates, fatty acyl-CoA, are utilized in peroxisomes. In our study, a typical PTS1, SKL, was fused with the C-terminal of CAT2-N fragment, guaranteeing its peroxisomal localization and possible function. As expected, the interaction between CAT2-N and ACX2/3 was in peroxisomes (Figure 3c,d), and transgenic plants with overexpression of CAT2-N-SKL had increased ACX activity and JA accumulation in response to B. cinerea B05.10 infection (Figure 5a,b). It is worth exploring the role of Arabidopsis CAT2-N in other plants, especially the related species such as Brassica rapa and Raphanus sativus, and potentially improve their resistance to necrotrophic pathogens by genetically manipulating CAT2-N.
Early reports showed that SA can bind to catalases in several plant species, including Arabidopsis and tobacco, and inhibit their H 2 O 2 -decomposing activity (Chen et al., 1993a(Chen et al., , 1993bPokotylo et al., 2019;Sanchez-Casas & Klessig, 1994). We also reported that SA inhibits CAT2 to repress B. cinerea B05.10-induced ACX activity for JA synthesis . In this study, we found that CAT2-N with no catalase activity interacted with and promoted ACX2/3, raising the possibility that antagonism of SA on JA biosynthesis would be diminished in plants with overexpression of CAT2-N.
Indeed, the 35S::CAT2-N-SKL plants showed less sensitivity to SA than the wildtype plant, evidenced by higher ACX activity, JA levels, and resistance to B. cinerea B05.10 ( Figure 6). These results also suggest that SA does not affect the interaction between CAT2-N and ACX2/3. However, which fragment of CAT2 has the SA-binding sites remains unknown and is worthy of further exploration.
In summary, our study reveals that CAT2-N interacts with and promotes ACX2/3 implicated in JA biosynthesis, and thus can be utilized to enhance plant resistance to B. cinerea. This truncated protein also partly relieves SA repression of JA biosynthesis during plant defence response to B. cinerea B05.10.

| Plant material and growth conditions
Arabidopsis thaliana ecotype Columbia was used in this study.

| Yeast two-hybrid assay
The plasmids pGBKT7-CAT2, pGADT7-ACX2, and pGADT7-ACX3 were as previously reported . The mutated CAT2,  were amplified by PCR-based side-directed mutagenesis and cloned into pGBKT7 vector at the BamHI site. The truncated CAT2, CAT2-N, and CAT2N+H were amplified by PCR from the full-length coding sequence of CAT2. The yeast transformation and growth were carried out according to our previous report . Primer sequences are listed in Table S1.
To prepare the proteins of mutated CAT2 and truncated CAT2, the coding sequences of mutated CAT2 and truncated CAT2 were cloned into the prokaryotic expression vector pET28a at the BamHI site, and then transformed into E. coli BL21 (DE3). The expression and purification of the proteins were performed according to our previous reports Zhang et al., 2020d).

| Detection of catalase (CAT) activity
The treated or untreated plants were ground to fine powder under liquid nitrogen, and suspended in freshly prepared, cold, protein extraction buffer (50 mM potassium phosphate buffer, pH 7.8, 0.2 mM EDTA-Na 2 , 0.1 mM ascorbic acid, 1% polyvinylpolypyrrolidone [PVPP]). After centrifugation at 12,000 × g for 10 min at 4 °C, the supernatant was transferred to a new tube for further use. The protein concentration was assayed by the Bradford method, and CAT activity was determined according to the published methods (Aebi, 1984;Li et al., 2020a). CAT activity was assayed by monitoring the consumption of H 2 O 2 at 240 nm. To determine the effect of 3-AT on catalase activity, different concentrations of 3-AT were treated with the purified CAT2 proteins, and then the catalase activity was assayed according to the above method.

| Bimolecular fluorescence complementation
For the bimolecular fluorescence complementation (BiFC) assays, the coding sequence of Arabidopsis CAT2 and truncated CAT2 were cloned into pSP-YNE, and the coding sequences of ACX2 and ACX3 were cloned into pSP-YCE. To label the peroxisomes in N. benthamiana leaves, mCherry fused with the SKL sequence were amplified from the PTS-RFP plasmid as we previously reported , and cloned into pEGAD vector at the AgeI and EcoRI sites, resulting in 35S::mCherry-SKL.
The resultant plasmids were introduced into Agrobacterium tumefaciens GV3101 and coinfiltrated the N. benthamiana leaves.
Three days after infiltration, the leaves were used to observe the YFP and mCherry fluorescent signals under a confocal laser scanning microscope (Carl Zeiss LSM710 META laser scanning microscope).

| Quantitative PCR
Treated or untreated plant leaves were collected for total RNA isolation, first-strand cDNA synthesis, and quantitative reverse transcription PCR (RT-qPCR) as described previously (Liu et al., 2018).
The constitutively expressed ACTIN2/8 gene was used as an internal control. All experiments were repeated at least three times. The primer sequences are listed in Table S1. The coding sequence of CAT2-N fused with the sequence of SKL (TCGAAGCTG) was amplified by PCR and inserted into pEGAD vector at the AgeI and EcoRI sites, resulting in 35S::CAT2-N-SKL.

The resultant plasmid was introduced into wildtype Arabidopsis by
A. tumefaciens GV3101-mediated transformation using the floral dip method. All the experiments were conducted with homozygous T 4 plants.

| Plant inoculation
Plant inoculation with B. cinerea and Pst DC3000 was carried out according to our previous reported method . For B. cinerea infection, B. cinerea strain B05.10 was cultured and inoculum was prepared as previously described (Song et al., 2014). The spore suspension at a density of 10 6 /ml was prepared, and 10 μl of the suspended spores was used to inoculate the 4-week-old plant leaves. Images of the infected plant leaves were captured 3 days after inoculation, and the relative lesion size was analysed according to our previously reported method . Infected and uninfected leaves were further used for ACX activity, JA levels, and RT-qPCR. For Pst DC3000 infection, the virulent strain Pst DC3000 was cultured in King's B medium containing 50 μg/ ml rifampicin at 28 °C. Four-week-old plant leaves were sprayed with Pst DC3000 (OD 600 = 0.01) suspended in 10 mM MgCl 2 and 0.02% Silwet. The bacterial growth was determined at 3 days after inoculation.

| Detection of ACX activity
Detection of ACX activity of the plants or purified proteins was performed according to our previously reported method Yuan et al., 2017). Briefly, OPC4-CoA was synthetized using OPC4 purchased from OlChemIm, and CoA and yeast acyl-CoA synthetase from a test kit (Roche) as previously reported (Li et al., 2005;Yuan et al., 2017). Purified or extracted plant protein was added to the reaction buffer (OPC4-CoA, 50 mM KPO 4 , pH 7.6, 50 µM flavin ad- To examine the ACX activity in plants, infected or uninfected plant leaves were ground to fine powder under liquid nitrogen and then resuspended in cold extraction buffer (50 mM KPO 4 , pH 7.6, 50 mM FAD, 100 µg/ml BSA). After centrifugation at 12,000 × g at 4 °C for 15 min, the supernatant was used to assay the ACX activity.

| Trypan blue staining
Trypan blue staining experiments were performed as described previously (Song et al., 2014;Yuan et al., 2017). Briefly, infected plant leaves were soaked in lactophenol-trypan blue staining solution (0.05% trypan blue, 25% lactic acid, 25% water-saturated phenol, 50% ethanol) at 37 °C for 1 hr. Chloral hydrate solution (2.5 g/ml) was used to wash the leaves to reduce the background. Images of trypan blue-stained leaves were captured by a camera, and the leaves were also observed under a microscope.

| Measurement of JA levels
JA levels were detected according to our previous reported methods Zhang et al., 2020d). Briefly, the infected and uninfected plant leaves were collected and ground into fine powder under liquid nitrogen. Dihydroxyjasmonic acid (DHJA, 20 ng) was added as an internal standard for JA. The purified samples were then methylated by diazomethane, resuspended in 100 µl of ethyl acetate, and analysed by gas chromatography-mass spectrometryselected ion monitoring (GC/MS-SIM) (Trace GC Ultra/ISQ; Thermo Fisher Scientific). The compounds were separated on an Rtx-5MS (30 m × 0.25 mm × 0.25 mm) column. The chromatographic parameters were as follows: 40 °C for 1 min after injection, followed by sequential temperature ramps of 25 °C/min to 150 °C, 5 °C/min to 200 °C, 10 °C/min ramp to 240 °C, and 240 °C for 10 min. The monitored ions were m/z 151 and 153 for JA and DHJA, respectively.

ACK N OWLED G EM ENTS
This work was supported by the National Natural Science Foundation of China (no. 32000150) and the Program for Innovative Research Team (in Science and Technology) in the University of Henan Province (21IRTSTHN019). The authors have no conflicts of interest to declare.

CO N FLI C T S O F I NTE R E S T
All the authors declare that they have no competing interests.

DATA AVA I L A B I L I T Y S TAT E M E N T
The data that support the findings of this study are available from the corresponding author upon reasonable request.

S U PP O RTI N G I N FO R M ATI O N
Additional supporting information may be found online in the Supporting Information section.