Analysis and cloning of the synthetic pathway of the phytohormone indole-3-acetic acid in the plant-beneficial Bacillus amyloliquefaciens SQR9
- Jiahui Shao†1, 2,
- Shuqing Li†2,
- Nan Zhang2,
- Xiaoshuang Cui2,
- Xuan Zhou2,
- Guishan Zhang1,
- Qirong Shen2 and
- Ruifu Zhang1, 2Email author
© Shao et al. 2015
Received: 4 June 2015
Accepted: 21 August 2015
Published: 4 September 2015
The plant growth-promoting rhizobacteria (PGPR) strain Bacillus amyloliquefaciens SQR9, isolated from the cucumber rhizosphere, protects the host plant from pathogen invasion and promotes plant growth through efficient root colonization. The phytohormone indole-3-acetic acid (IAA) has been suggested to contribute to the plant-growth-promoting effect of Bacillus strains. The possible IAA synthetic pathways in B. amyloliquefaciens SQR9 were investigated in this study, using a combination of chemical and genetic analysis.
Gene candidates involved in tryptophan-dependent IAA synthesis were identified through tryptophan response transcriptional analysis, and inactivation of genes ysnE, dhaS, yclC, and yhcX in SQR9 led to 86, 77, 55, and 24 % reductions of the IAA production, respectively. The genes patB (encoding a conserved hypothetical protein predicted to be an aminotransferase), yclC (encoding a UbiD family decarboxylase), and dhaS (encoding indole 3-acetaldehyde dehydrogenase), which were proposed to constitute the indole-3-pyruvic acid (IPyA) pathway for IAA biosynthesis, were separately expressed in SQR9 or co-expressed as an entire IAA synthesis pathway cluster in SQR9 and B. subtilis 168, all these recombinants showed increased IAA production. These results suggested that gene products of dhaS, patB, yclB, yclC, yhcX and ysnE were involved in IAA biosynthesis. Genes patB, yclC and dhaS constitute a potential complete IPyA pathway of IAA biosynthesis in SQR9.
In conclusion, biosynthesis of IAA in B. amyloliquefaciens SQR9 occurs through multiple pathways.
Promotion of plant growth by Bacillus strains inhabiting the rhizosphere is well documented [1–4]. The plant growth-promoting effect of rhizospheric bacilli results from the synergy of several factors, including the production of phytohormones such as indole-3-acid (IAA), the secretion of extracellular phytase under conditions of phosphate limitation and in the presence of phytate [5, 6], and the emission of volatile compounds [2, 7, 8].
It appears that the secreted IAA plays an important role in the plant-growth-promoting effect of some plant-beneficial bacteria [9–11]. IAA is a common phytohormone with the capacity to regulate nearly every aspect of plant growth and development, such as cell division, elongation, fruit development and senescence [12–15]. IAA produced by plant-growth-promoting bacteria also acts in the rhizosphere, including stimulation of root-hair formation by increasing the number and length of lateral and primary roots when it is within a certain concentration range [16–18]. IAA synthesis in bacteria may lead to increased rooting, as observed in studies with Azospirillum mutants with altered IAA production . This increased rooting enhanced plants’ water and nutrient uptake and root exudation, which in turn stimulated bacterial root colonization. A study by Ahmed and Hasnain  demonstrated that inoculation of two IAA-producing Bacillus strains could significantly increase the shoot length, root length and number of leaves on the plant compared to non-inoculated treatments, suggesting the possible use of IAA-producing bacteria as effective plant-growth-promoting inoculants.
The ability to synthesize IAA is a common trait in rhizospheric bacteria, and tryptophan has been identified as a main precursor for IAA biosynthesis pathways [21, 22]. To date, studies on the key genes or proteins involved in IAA production are few and have mostly been focused on a single specific gene or protein in a biosynthetic pathway. In plants, four tryptophan-dependent IAA synthesis pathways have been proposed, the indole-3-pyruvic acid (IPyA), indole-3-acetamide (IAM), indole-3-acetonitrile (IAN), and tryptamine (TAM) pathways, and they have also been postulated in bacteria [23, 24]. The IPyA pathway is thought to exist in both plants and bacteria, including phytopathogenic and beneficial bacteria . The gene encoding the key enzyme indole-3-pyruvate decarboxylase (IPDC), a decarboxylase that converts IPyA into indole-3-acetylaldehyde, has been identified and characterized in Az. brasilense, Enterobacter cloacae, and Pseudomonas putida [18, 25–27]. In these organisms, inactivation of this pathway resulted in lower IAA production, up to 90 % reduction in Az. brasilense , indicating the importance of the IPyA pathway in auxin production. However, the bacterial gene responsible for the aldehyde oxidation step of the IPyA pathway remains elusive. The presence of the IPyA pathway in some phytopathogens was proposed based on the identification of the corresponding intermediates [29, 30]. The IAM pathway is the best-characterized pathway in bacteria [31–33]. This two-step pathway is catalyzed by the enzymes tryptophan-2-monooxygenase (IaaM) and IAM hydrolase (IaaH), encoded by the iaaM and iaaH genes, respectively [23, 24]. The TAM pathway has been suggested in B. cereus and Azospirillum by the identification of tryptophan decarboxylase activity  and the conversion of exogenous tryptophan to IAA , but the genes involved in this pathway still need to be confirmed in bacteria. The biosynthesis of IAA via IAN has been extensively studied in plants, but it has not been characterized in bacteria. The steps leading to the conversation of tryptophan to IAN are still a matter of debate, but the last step of this pathway, converting IAN into IAA, was catalyzed by a nitrilase . The possible IAN pathway in bacteria such as Alcaligenes faecalis was suggested due to the detection of nitrilase with specificity for indole-3-acetonitrile [37, 38]. Further, the nitrilase in P. syringae B728a is capable of hydrolyzing indole-3-acetonitrile to IAA, allowing this strain to use indole-3-acetonitrile as the nitrogen source . Tryptophan-independent pathway was also suggested although no enzyme involved in this pathway has been characterized. In Arabidopsis thaliana, tryptophan-independent pathway was suggested based on the observation that tryptophan synthesis mutants increased IAA conjugates [40, 41]. In Az. brasilense, feeding experiments with labeled substrates revealed that 90 % of the IAA is synthesized via the tryptophan-independent pathway when tryptophan was absent in the medium .
Though much work has been performed on the IAA synthesis pathway in both plants and bacteria, as described above, the details of the biosynthetic pathways utilized by Gram-positive bacteria remain less clear. Stimulation of IAA production by tryptophan was previously described for Gram-positive bacteria . In the phytopathogenic Rhodococcus fascians, the main biosynthetic route for IAA is the IPyA pathway, and the ipdC gene was functionally identified and expressed in Paenibacillus polymyxa E681 [42, 43]. In B. amyloliquefaciens FZB42, a fivefold increase in IAA secretion was recorded in the presence of tryptophan . Deletion of the gene ysnE, which encodes a putative tryptophan acetyltransferase, results in a 72 % decrease of IAA production in FZB42 . Meanwhile, an FZB42 mutant with a deletion of the putative nitrilase gene yhcX only produced 50 % of the wild type level of IAA . These results indicated that the IAA synthesis in B. amyloliquefaciens FZB42 was tryptophan-dependent and that the IAN pathway and another uncharacterized pathway involving tryptophan acetyltransferase were the main routes for IAA biosynthesis .
Strains and plasmids used in this study
Strains or plasmids
Reference or source
E. coli top10
F-mcrAΔ (mrr-hsdRMS-mcrBC) ψ80lacZΔM15Δ lacX74 nupG recA1 araD139Δ (ara-leu) 7697 galE15 galK 16 rpsL (StrR) end A1λ-
B. amyloliquefaciens SQR9 with pUBC19-P43-patB (kanr)
B. amyloliquefaciens SQR9 with pUBC19-P43-yclC (kanr)
B. amyloliquefaciens SQR9 with pUBC19-P43-dhaS (kanr)
B. amyloliquefaciens SQR9 with pUBC19-P43-BCS (kanr)
B. amyloliquefaciens SQR9 with pUBC19-P43 (kanr)
B. subtilis 168 with pUBC19-P43-BCS (kanr)
B. subtilis 168 with pUBC19-P43 (kanr)
Ampr Kmr; B.subtilis-E. coli shuttle vector
pUBC19 containing P43 promoter
pUBC19 containing P43 promoter and patB
pUBC19 containing P43 promoter and yclC
pUBC19 containing P43 promoter and dhaS
pUBC19 containing P43 promoter and fusion fragments for expression
pUBC19 containing dhaS
pUBC19 containing yclC
pUBC19 containing ysnE
Screening of genes likely to be involved in IAA biosynthesis in the B. amyloliquefaciens SQR9 genome
Possible B. amyloliquefaciens SQR9 genes involved in tryptophan dependent IAA production
IAA synthesis pathways
Enzymes proposed in each step
Putative genes in SQR9 and accession numbersa
patB (V529_31110), bioA(V529_17980), yotD(V529_21800)
ydaP(V529_04190), pycA (V529_14260), padC(V529_34370), yclB(V529_03390), yclC(V529_03400)
aldX(V529_39560), dhaS(V529_19360), yfmT(V529_06950), ywdH(V529_29500)
ydaP(V529_04190), pycA(V529_14260), padC(V529_34370), yclB(V529_03390), yclC(V529_03400)
aldX(V529_39560), dhaS(V529_19360), yfmT(V529_06950), ywdH(V529_29500)
Transcriptional responses to tryptophan identified the genes involved in tryptophan-dependent IAA biosynthesis of B. amyloliquefaciens SQR9
Gene knockout mutants revealed the key genes and pathways contributing to IAA biosynthesis of B. amyloliquefaciens SQR9
To confirm their contribution to IAA production in B. amyloliquefaciens SQR9, these six genes were individually deleted, and the IAA productions of these mutants were measured and compared with the wild-type SQR9 (Fig. 1b). All mutant strains showed growth curves comparable to that of wild-type SQR9. Indole-3-acetic acid was defined in SQR9 supernants by monitoring the transition of the parent molecular ion m/z 176 to the principle daughter ion m/z 130 in LC/MS analysis. Quantification of the IAA amounts present in culture filtrates of gene knockout mutants showed that strains ΔysnE, ΔdhaS, ΔyclC, and ΔyhcX produced only 14, 23, 45, and 76 % of the wild type SQR9 IAA production level, respectively (Fig. 1b), whereas strains ΔpatB and ΔyclB produced IAA at levels similar to wild-type SQR9. Complementation of the four mutants with the B. amyloliquefaciens- Escherichia coli shuttle vector pUBC19 carrying the corresponding deleted genes restored the IAA production (Fig. 1b). These results suggested that the pathway including tryptophan acetyltransferase was an important route for IAA biosynthesis in SQR9. The IPyA and TAM pathways also contributed substantially, but the IAN pathway only slightly contributed to IAA production in SQR9.
Cloning and expression of the indole-3-pyruvic acid pathway and related genes for IAA biosynthesis
Taking advantage of the whole-genome sequence of SQR9, we used genomic scanning and related studies to investigate the key genes in the IAA biosynthesis pathways. The IPyA, TAM, and IAN pathways, as well as an uncharacterized pathway, were believed to participate in IAA biosynthesis of SQR9, according to the analysis of reverse transcription and of gene-knockout mutations. The uncharacterized IAA biosynthesis pathway appeared to be the most important route in SQR9 because IAA production by the ysnE gene knockout mutant was only 14 % of the wild type. The IPyA and TAM pathways also made substantial contributions, but the IAN pathway only contributed minorly IAA production in SQR9.
Genes involved in the IAM pathway, which has been described mainly in phytopathogenic bacteria, were not detected in the SQR9 genome. This two-step pathway has been reported for other PGPR strains. The IAN pathway has been suggested in Al. faecalis [37, 38] and P. syringae B728a  and was believed to contribute to IAA production in B. amyloliquefaciens FZB42 . In B. amyloliquefaciens FZB42, YhcX was predicted to act as a nitrilase based on its similarity to nitrilase 2 of A. thaliana, which catalyzes the final step of the IAN pathway . The yhcX gene was also detected in the SQR9 genome, but knockout of this gene only led to a 24 % decrease in IAA production. IAA production in the ysnE gene mutant was only 14 % of the wild type, but this specific metabolic process is poorly studied. The predicted product of the ysnE gene belongs to the N-acetyltransferase superfamily of various enzymes that catalyze the transfer of an acyl group to a nitrogen atom on the acceptor molecule. In B. amyloliquefaciens FZB42, this protein is similar to a putative tryptophan acetyltransferase gene localized within the tryptophan biosynthesis gene cluster in Az. brasilense and has been predicted to participate in tryptophan-dependent IAA production [9, 51, 52], while in Bacillus strains, this gene locates away from the tryptophan biosynthesis gene cluster. We deduced that the ysnE gene product is one of the most important intermediates in B. amyloliquefaciens strains, and in-depth study of the role of this gene in IAA biosynthesis will have great significance.
Most beneficial bacteria produce IAA via the IPyA pathway . In our study, gene products of patB, yclC and dhaS were proposed to constitute the entire IPyA pathway in SQR9. Both homologous expression in B. amyloliquefaciens SQR9 and heterologous expression in B. subtilis 168 successfully led to increased IAA production with tryptophan supplied in the medium. In Bacillus strains, the patB gene was defined as a putative aminotransferase in the aspartate aminotransferase family. This family belongs to the pyridoxal phosphate (PLP)-dependent aspartate aminotransferase (AAT) superfamily, whose members catalyze four types of reactions: transamination (movement of amino groups), racemization (redistribution of enantiomers), decarboxylation (removing COOH groups), and various side-chain reactions. The major groups in this conserved domain correspond to aspartate aminotransferase a, b, and c and to other amino acids, including aromatic amino acids, such as tryptophan. A previous study constructed two AAT mutants of Rhizobium meliloti and revealed that neither was essential for the biosynthesis of IAA in the absence of exogenous tryptophan but both contributed to IAA biosynthesis when high levels of exogenous tryptophan were present . The yclC gene, located in the same operon as yclB, was considered a hypothetical protein, possibly encoding a decarboxylase from the UbiD family, which contains several different decarboxylases. The gene product of yclC was predicted to be an indole-3-pyruvate decarboxylase, which has no significant similarity with the reported indole-3-pyruvate decarboxylase in other organisms. Neither do the yclC gene has significant similarity with recent reported flavin monooxygenase YUCCA1 that directly converts IPyA to IAA in Arabidopsis [54–56]. The gene responsible for the aldehyde oxidation step of the IPyA pathway in bacteria remains elusive. DhaS, similar to aldehyde dehydrogenase, which likely catalyze the final reaction of the IPyA pathway, has not been considered to be involved in IAA synthesis in B. amyloliquefaciens FZB42 [9, 51]. However, in SQR9, the gene product of dhaS is demonstrated to be involved in IAA synthesis because IAA production of this gene knockout mutant was only 23 % of the wild type. The differences between SQR9 and FZB42 strains, which belong to the same species, might be caused by individual differences, as strain SQR9 could produce much more IAA with tryptophan supplied than strain FZB42 reported by Idris et al. ; IAA produced by mutant strains of FZB42 were quantified without tryptophan supplied, although very few, bacteria synthesis tryptophan from indole itself , while in our study, IAA production was always quantified with tryptophan supplied .
The patB gene was up regulated in reverse-transcription analysis, but its gene deficient mutant strain did not show lower IAA production, and the over expression experiment confirmed that this gene participates in the IPyA pathway. This suggests that although it responds to tryptophan sensitively, the gene product of patB might not be the solely gene responsible for the aminotransferase reaction. The yhcX gene encoding the putative nitrilase was markedly up regulated in the reverse-transcription analysis, whereas ΔyhcX only showed a 24 % decrease in IAA production. These confusing phenomena might be explained as follows: (1) it is possible that strain SQR9 possesses several different isoforms of the enzyme for IAA synthesis, each able to utilize multiple substrates, as Kittell et al.  reported that aromatic amino acid aminotransferase can act upon all three aromatic amino acids. Furthermore, although ipdC-encoded indolepyruvate decarboxylases from some bacteria have high affinity for indolepyruvate, they can also utilize phenylpyruvate, pyruvate and benzoylformate as substrates [42, 58–60]. (2) As reported for B. megaterium, several genes that encode isozymes of glucose dehydrogenase are known , and the aminotransferase and nitrilase steps contain multiple enzymes acted as isozymes. When the patB and yhcX genes were inactivated, other genes functioned as isozymes. In bacteria, nitrilases belong to a large family. Branch I Nitrilases are known to have true nitrilase activity [62, 63], which may be implicated in IAA biosynthesis. (3) The gene product of patB acts as an aminotransferase, converting tryptophan to indole-3-pyruvic acid, suggesting that patB gene product is not only a likely immediate precursor for IAA biosynthesis but also a precursor for indolelactic acid (ILA) and tryptophol (Tol), which have been identified as products of physiological origin in Agrobacterium tumefaciens . (4) There are different pathways to synthesize IAA in bacteria, the break down of one pathway could enhance the others. Thus, we concluded that the primary roles of the genes identified in this study might not be the production of IAA; rather, their involvement in the IAA synthesis pathway is incidental. Furthermore, we speculate that each step of the IAA synthesis pathway might contain several isozymes. Therefore, the roles of the reactions catalyzed by the six gene products in IAA biosynthesis in SQR9 remain to be elucidated. Feeding experiments, double and triple mutant analysis, appropriate labeling studies and identification of biosynthetic intermediates will be required to uncover the metabolic route for tryptophan-dependent IAA synthesis in SQR9.
In conclusion, the results presented here identified six genes involved in IAA biosynthesis of B. amyloliquefaciens SQR9 by transcription and IAA quantification analysis of the relevant mutants. The predicted tryptophan-dependent IAA biosynthesis pathways in SQR9 were shown in Fig. 3, and pathways such as IAN, TAM, IPyA and an uncharacterized pathway, which was supposed to be the most important one, are suggested to appear in this strain. Moreover, a possible IPyA pathway for IAA biosynthesis, consisting of patB, yclC and dhaS, was confirmed through homologous and heterologous expression in B. amyloliquefaciens SQR9 and B. subtilis 168. This study deepened our understanding of IAA biosynthesis in B. amyloliquefaciens SQR9 and provided molecular evidence for genetic modification of Bacillus spp. for better agricultural application. The overexpression strain of SQR9 produced more IAA and this strain has the potential to be more efficiently to promote plant growth.
Strains and growth conditions
The strains and plasmids used in this study are described in Table 1. B. amyloliquefaciens SQR9 (China General Microbiology Culture Collection Center, CGMCC accession no. 5808) was isolated from the rhizosphere of cucumber. E. coli top10 was used as the host for all plasmids, and B. subtilis 168 was used as the host for heterologous expression of the IAA biosynthesis pathway genes. B. amyloliquefaciens SQR9 and B. subtilis 168 were grown at 30 °C in low-salt Luria–Bertani (LLB) medium (peptone, 10 g L−1; yeast extract, 5 g L−1; NaCl, 5 g L−1) solidified with 1.5 g 100 mL−1 agar; when necessary, 5 μg mL−1 chloramphenicol (Cm) or 20 μg mL−1 kanamycin (Km) was added. E. coli top10 was grown in LLB medium at 37 °C; when required, Cm was added to a final concentration of 12.5 μg mL−1 or Km to 30 μg mL−1. For IAA production, the bacteria were grown for 72 h in Landy medium  containing 3 mM l-tryptophan at 25 °C and 90 rpm.
Genome analysis of genes involved in IAA production in SQR9
Based on the whole-genome nucleotide sequence of SQR9 (NCBI accession no. CP006890), the function of all protein-coding genes in SQR9 against reference genomes of B. amyloliquefaciens FZB42  and B. subtilis 168  was obtained by using BLASTP (parameters: e-value: 1e-5, coverage >60 %, identity >50 %). The genes were identified according to their deduced protein domains, which show putative enzyme activities already known in IAA metabolism.
Reverse transcription analysis of genes involved in IAA synthesis
RNA was isolated from B. amyloliquefaciens SQR9 cells fermented in Landy medium with or without 3 mM l-tryptophan at 65 h post-inoculation. The cells were harvested by centrifugation at 4 °C (10 min, 5000×g). Total RNA samples were extracted using an RNAiso Plus kit (TaKaRa, Dalian, China) according to the manufacturer’s protocol. RNA was reverse-transcribed into cDNA in a 20-μL reverse transcription system (TaKaRa, Dalian, China) according to the manufacturer’s instructions.
Transcription levels of genes potentially involved in SQR9 IAA biosynthesis with or without tryptophan in the growth medium were measured by quantitative reverse transcription PCR (qRT-PCR) using a SYBR Premix Ex Taq kit (TaKaRa, Dalian, China). The primers used to amplify these genes are listed in Transcription analysis part of Additional file 2: Table S1. The recA gene of SQR9 was served as an internal control. Reactions were carried out on an ABI 7500 system under the following conditions: cDNA was denatured for 10 s at 95 °C, followed by 40 cycles of 5 s at 95 °C and 34 s at 60 °C. The 2−ΔΔCT method was used to analyze the qRT-PCR data.
Gene knockout by allelic exchange
To delete the genes of B. amyloliquefaciens SQR9, fragments of approximately 1 kb in length both upstream and downstream of each target gene were amplified. The 1.1-kb chloramphenicol resistance gene (Cmr) was amplified from plasmid pNW33n with primers, which were partially overlapped with the upstream and downstream fragments of each target gene. Upstream and downstream fragments were fused with the chloramphenicol resistance gene by overlap extension. Primers used in this experiment are shown in Gene knockout part of Additional file 2: Table S1. The 25 µl mixture for the first step of the overlapping PCR is as follows: 13.2 µL water, 5 µL PrimeSTAR buffer (5×), 2 µL dNTP mix (2.5 mM each), 1.5 µL (15 ng) upstream fragment, 1.5 µL (15 ng) downstream fragment, 1.5 µL (15 ng) Cmr fragment, and 0.3 µL PrimeSTAR HS DNA polymerase. The PCR program was as follows: 98 °C for 2 min, 98 °C for 10 s, 56 °C for 10 s and 72 °C for 3.5 min, 15 cycles. The second step of overlapping PCR, the mixture included 16.7 µL water, 5 µL PrimeSTAR buffer, 2 µL dNTP mix, 1 µL forward primer for the upstream fragment, 1 µL reverse primer for the downstream fragment, 1 µL unpurified product from the first PCR step, and 0.3 µL PrimeSTAR HS DNA polymerase. The PCR program was as follows: 98 °C for 2 min, 98 °C for 10 s, 52 °C for 10 s and 72 °C for 3.5 min, 32 cycles. All PCR products were gel-purified using an AxyPrep DNA gel purification and extraction kit (Axygen, Hangchow, USA).
The fused fragments for the target genes were individually transformed into competent cells of B. amyloliquefaciens SQR9 , and the transformants were selected on LLB agar plates containing 5 μg mL−1 Cm. The correct mutants were verified by PCR using the primer sets in Mutant verification part of Additional file 2: Table S1.
Complementation of the disrupted genes
Plasmid pUBC19-X (X represents genes of dhaS, yclC, yhcX and ysnE) were constructed to complement each deleted gene in SQR9 mutants. Primers used in this study are shown in Complementary experiment part of Additional file 2: Table S1. The dhaS and ysnE genes (including their promoters), bordered by primer-introduced PstI and BamHI sites, were amplified from SQR9 genomic DNA using the primers dhaScF/dhaScR and ysnEcF/ysnEcR. The yclC and yhcX genes (except for their promoters) bordered by primer-introduced PstI and KpnI sites (yclCcF/yclCcR and yhcXcF/yhcXcR) were amplified. After purification and digestion with the corresponding restriction enzymes, the fragments of dhaS and ysnE were cloned into the B. amyloliquefaciens-E.coli shuttle vector pUBC19; yclC and yhcX gene fragments were ligated into the pUBC19-P43 vector, which is described in a subsequent section, under the control of the P43 promoter from B. subtilis 168 for their promoters remain uncertain. Plasmids were sequenced to confirm their fidelity and then transformed into each corresponding mutant strain of SQR9 to obtain complemented strains.
IAA production analysis
Wild-type and gene knock-out mutants of SQR9 and B. subtilis 168 strains were propagated overnight in 3 mL Landy medium, and then, 1 ml aliquots were transferred into 100 mL Landy medium supplied with 3 mM l-tryptophan. After incubation for 72 h, the density of each culture was measured spectrophotometrically at 600 nm, each of the cell culture was adjusted to OD600 = 5.0 with sterilized water and then the cells of SQR9, B. subtilis 168 and mutant strains were removed by centrifugation (5000×g, 20 min, 4 °C). Next, 50 µL culture supernatant of each strain was subjected to ELISA analysis with the IAA ELISA KIT (Cloud-Clone Crop. USA), and the IAA content was quantified. Liquid cultures (100 mL) of each strain were adjusted to pH 2.5 with 1.0 M HCl and extracted three times with ethyl acetate (1:3, v/v). The organic solvents were vacuum-dried at 37 °C and then dissolved in 3 ml methanol. The extract samples were filtered through a 0.45-µm membrane before analysis. Extracted samples were separated with Reverse Phase High Performance Liquid Chromatography (RP-HPLC) using a reversed-phase C18 analytical column (9.4 by 150 mm; Agilent Technologies, Santa Clara, CA). The mobile phase was methanol-0.1 % acetic acid (60/40) at a flow rate of 0.4 mL min−1 for 25 min at 220 nm using a UV detector. IAA was quantified by integrating the areas under peaks with the help of authentic IAA from Sigma. The molecular weight of IAA identified by RP-HPLC was determined by an Agilent 6410 triple quadrupole LC/MS apparatus (Agilent Technologies). The electrospray needle was operated at a spray voltage of 4.5 kV and a capillary temperature of 300 °C. The mobile-phase components were methanol-0.1 % acetic acid (60/40) at a flow rate of 0.4 ml min−1. Data acquisition was done in the positive ion mode.
Expression of the identified genes or indole-3-pyruvic acid pathway cluster of SQR9
Primers P43F/P43R (Additional file 2: Table S1) were used to clone the P43 promoter sequence from B. subtilis 168 chromosomal DNA; the BamHI site was introduced into the forward primer P43F, KpnI and PstI sites were introduced into the reverse primer P43R. The P43 fragment was inserted into the shuttle vector pUBC19 between the BamHI and PstI sites, and the recombinant plasmid was designated as pUBC19-P43 (Fig. 2). Genes for expression were PCR-amplified with the primers shown in Additional file 2: Table S1. For single gene expression, a KpnI site was introduced into the forward primer and a PstI site was introduced into the reverse primer of each gene. For gene cluster expression, a KpnI site was introduced into the forward primer of patB, and a PstI site was introduced into the reverse primer of dhaS. The PCR fragments for gene cluster expression were spliced by overlap extension described above. Gene fragments and the pUBC19-P43 plasmid were digested with KpnI and PstI and then ligated together, and the recombinant plasmids were named pUBC19-P43-patB, pUBC19-P43-yclC, pUBC19-P43-dhaS and pUBC19-P43-E (Fig. 2).
Plasmids pUBC19-P43-patB, pUBC19-P43-yclC and pUBC19-P43-dhaS were transformed into the competent cells of B. amyloliquefaciens SQR9  to obtain the strains patB-E (pUBC19-P43-patB in SQR9), yclC-E (pUBC19-P43-yclC in SQR9) and dhaS-E (pUBC19-P43-dhaS in SQR9). Plasmids pUBC19-P43-E and pUBC19-P43 (as empty vector control) were transformed into the competent cells of SQR9 and B. subtilis 168  to obtain the strains SQR9-E (pUBC19-P43-E in SQR9), SQR9-CK (pUBC19-P43 in SQR9), 168-E (pUBC19-P43-E in B. subtilis 168), and 168-CK (pUBC19-P43 in B. subtilis 168). Transformants were grown in LLB medium containing 20 µg mL−1 km. For the detection of IAA production, transformants were incubated in Landy medium supplied with tryptophan, and the cultures were analyzed with HPLC and ELISA as described above.
Nucleotide sequence accession numbers
The GenBank accession numbers for the genes in IAA biosynthesis in the SQR9 genome (NCBI accession no. CP006890) are shown in Table 2. The GenBank accession numbers for the phy gene and the alsRSD gene cluster are V529_21880, V529_35850, V529_35860 and V529_35870, respectively.
JS carried out the molecular genetic studies, participated in genomic analysis, plasmid design, gene knockout and expression,and drafted the manuscript. SL carried out genomic analysis, plasmid design and transcription analysis. NZ participated in the sequence alignment and genomic analysis. XC and XZ participated in IAA production analysis. GZ participated in gene knockout. QS participated in the design of the study and performed the statistical analysis. RZ conceived the study, and participated in its design and coordination, and helped to draft the manuscript. All authors read and approved the final manuscript.
This research was financially supported by the Chinese Ministry of Science and Technology (2013AA102802), the Fundamental Research Funds for the Central Universities (KYZ201408) and the China Postdoctoral Science Foundation (2014M560430), RZ and QS were also supported by the 111 Project (B12009) and the Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interest.
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