Print version ISSN 1517-8382
Braz. J. Microbiol. vol.43 no.2 São Paulo Apr./June 2012
Neelam TankI; Narayanan RajendranII; Baldev PatelI; Meenu SarafI, *
IDepartment of Microbiology, University School of Sciences, Gujarat University of Sciences, Gujarat University, Ahmedabad 380 009, Gujarat, India
IIMicrobiology, Department of Biology, MASC, Kentucky State University, Frankfort, Kentucky, 4060, USA
Microbial siderophores confiscate the available ferric ions around the roots and trigger a reaction resulting in plant growth promotion. In our study, a high level of siderophore production was observed from a newly isolated Pseudomonas sp. from the rhizosphere of Chickpea plants. Under an iron depleted condition in Standard Succinic acid medium a 1000 µgmL-1 of siderophore production was achieved. Increasing the concentration of iron showed an inverse relationship between growth and siderophore production. Fourier Transform Infrared Spectroscopy (FTIR) analysis of the purified crystals, its UV spectral analysis and High Pressure Liquid Chromatography (HPLC) revealed the identity of the siderophore as similar to that of pyoverdin with distinctive characters. Electron spray ionization mass spectroscopy (ESIMS) shows presence of abundance of A1 ions (419 m/z) and branching of amino acids from B1-B5. This pyoverdin contains a cyclic tetra peptide but Serine and Arginine are missing. Based on our analysis and deviations from the reported structure of pyoverdin it is suggested that this pseudomonas produces distinctly characterized pyoverdin siderophore.
Key words: Fluorescense, hydroxamates, collision activation, pyoverdin, Pseudomonas
Iron is essential for processes such as respiration, photosynthesis and nitrogen fixation but microbes have difficulty obtaining enough iron to support their growth because iron is in immobilized form of insoluble ferric hydroxide in soil and cannot be transported in the cells (1). Ability to produce siderophores by an organism under iron limiting conditions can promote plant growth by directly supplying iron for plant utilization and by removing iron from the environment for the growth of phytopathogens thereby reducing their competitiveness (2). It has been studied that yellow green siderophore producing Pseudomonas species exert biocontrol effect on phytopathogens there by enhancing plant growth. Pseudomonas fluorescens and P. putida produce siderophores of two general types, Pyochelin and Pyoverdin. Each siderophore has a specific role in metal acquisition. Pyochelins are phenolate siderophores derived from salicylic acid and cysteine. Pyoverdins are water soluble pigments that fluoresce yellow-green under ultraviolet light. All pyoverdins are structurally similar containing of a chromophore moiety, which gives bacteria its fluorescent nature, and a dicarboxylic acid (4). More than 40 pyoverdin peptide chain compositions have been identified in the group containing arginine dehydrolase positive, saprophytic or opportunistic animal pathogenic fluorescent Pseudomonas species. The chemistry and biology of different siderophores have been discussed by Hider and Kong (3).
Pyoverdins are now used as a major tool in identification, systematics, and characterization of closely related pseudomonad species. There are different siderovars, regroup strains that produce pyoverdins with same peptide chain, in certain species. P. fluorescens has 19 siderovars where as P. putida has 13 siderovars (5).Each siderophore has a specific role in metal acquisition. Puesdomonas PAO1 secretes both types of siderophores, Pyoverdin , which exhibit binding affinity for iron and Pyochelin which shows affinity for other metals and has a biocontrol potential. Siderophores from different bacteria are designated and named on the basis of name of organism for eg. Enterobactin, Agrobactin , Rhizobactin etc. In this study, we isolated a distinctively characterized siderophore produced by a Pseudomonas sp. isolated earlier from rhizosphere of Cicer arietinum and biochemically characterized its type and variety in order to reveal the identity of the type of siderophore.
MATERIALS AND METHODS
Bacterial strain, culture conditions and growth study
Bacterial strain of P. fluorescens was isolated and identified by 16sRNA from the rhizosphere of chickpea crop. This isolate was screened for Plant Growth Promoting potential after studying its various PGP (Plant Growth Promoting ) traits as reported by us earlier (6). The isolate was maintained on nutrient agar at 5 ºC until used. The sequence is deposited in Gene Bank Accession No. MSC2 HQ179576.
Induction and estimation of siderophores in MM9 medium
Actively growing inoculum of Pseudomonas culture was added to MM9 medium (8) and incubated on rotary shaker (200 rpm) and generation time calculated. Simultaneous induction of siderophore production was also checked by taking 1 mL of cell free supernatant was added with 1 mL of Chromeazurol S (CAS) shuttle solution. Amount of siderophore units was calculated as Percentage of Siderophore Unit = (Ar-As)/Ar x 100 (where Ar = absorption of Reference and As = Absorption of Sample) as reported earlier(7). Induction was also confirmed by Agar Well method where the culture supernatant was added into bored-wells in agar plates of MM9 medium supplemented with Casamino acids and CAS dye . Presence of siderophore can be checked as zone of discoloration of CAS dye around the well after 24 h of incubation at 300C.
Deferrated Standard Succinic Medium (SSM) was inoculated with 24 h old culture and incubated at 30 ºC. Siderophore production was checked after 24 h and 30 h when culture attained its stationary phase. Detection was done using CAS shuttle solution as described by (8). A simultaneous change in pH was also checked. Type of siderophore was checked by performing various methods like Arnows (9) for detecting catecholate type of siderophore and Csaky's (10) method for detecting hydroxamate type of siderophore.
Effect of different FeCl3 concentration on siderophore production and Fluorescence
In order to determine the threshold level of ferrous at which siderophore biosynthesis is repressed in fluorescent Pseudomonas, the deferrated liquid succinic acid medium and then externally added with different ferrous concentration ranging between 0-20 µM. This was then inoculated and incubated for 30 hours at 30ºC and checked for production of siderophores. Fluorescence produced by isolates at different FeCl3 concentrations was estimated by using Quinine Bisulphate method (11) using Spectrofluorimeter (Hitachi, Model F-2000) at an excitation of 295 nm and emission at 485 nm.
Crystallization and FTIR studies of siderophores
The produced siderophore was crystallized to study the chemical structure. The 30h old culture was centrifuged and cell-free supernatant was added with saturated FeSO4 solution to get maximum ferreted siderophores. The pH was adjusted to 3.0 with H2SO4 and 50 % ammonium sulphate solution was added to deproteinize. The aqueous phase was concentrated in a rotary vacuum evaporator and set aside in cold to crystallize. The filtrate was neutralized, reduced to dryness and extracted in dry hot methanol. The crystals were then separated out on Whatman filter paper no. 44. Crystals obtained were then used for their FTIR analysis and compared with the FTIR of standard hydroxamic acid crystals(12).
Partial purification of siderophore for spectral analysis
Culture was grown in deferrated SSM , the cell free supernatant was collected and its pH was adjusted to 6.0 with 6 M HCL. This supernatant was then passed through XAD-4 column (25x2.5 cm) with a flow rate of 60 mL in 1 h. After complete removal of the fluorescence from the supernatant, the column turns green proving the adsorption of fluorescence pigment on the resin. (13). Six different fractions of 1.5 mL each were collected and studied for the presence of fluorescence under U.V. light. The peak of absorbance was checked using UV visual spectrophotometer. Influence of pH on the shift of absorption peak was checked on partially purified pyoverdins at various pH (3.0, 5.0, 7.0 and 10.0) and compared with standard P. fluorescens at pH 7.0 and 3.0 according to Bultreys et al,(13) who has linked the siderophore production to pH.
Detection and Comparison of Pyoverdins by HPLC and MS
After incubation for 30h, the culture was centrifuged for 20 min. This was then filtered through 0.2 µm membrane filter and pH adjusted to 5.0 - 5.5. Pyoverdin production was estimated by measuring the absorbance at 403 nm. By using HPLC, the retention times (RT) of peaks with comparable heights were analyzed. The HPLC analyses were performed with Nucleosyl C18 columns and a Waters 2190 system.
The molecular mass of the pyoverdin was determined by mass spectrometry using Electron spray Ionization Solvent H20, CH3OH, CF3COOH 50:50:1 capillary temperature 230ºC spray voltage 3.4 - 3.6 kV (15).
RESULTS AND DISCUSSION
Induction and Estimation of siderophore in the medium
The isolate entered into log phase after 8h of incubation on shaker in deferrated MM9 medium which was 4 h later than that in nutrient medium and achieved its stationary phase after 30h (Figure 1). Here glucose served as sole C source and glutamic acid served as sole N source. Similar results were also obtained by Carson et al. (13) when S. meliloti was grown in MSM-YE medium, which showed an increase MGT in absence of iron in the medium. The result shows that siderophore production was induced along with the growth of the isolate (Figure 2), and was observed just after 8h when the culture entered into logarithmic phase and continued to increase until the culture attained stationary phase i.e. 30h. Results show that hydroxamate types of siderophores, with high ferrous affinity, are present in the supernatant. Siderophore units (%) in the culture broth were found to be 85 % (Table 1). Sayyed et al. (6) also found presence of 87 % of siderophore units in the medium.
Siderophore production by the isolate carried out on solid CAS blue agar showed a 22 mm clear zone of orange colour representing iron chelation. Supernatent from culture was tested with Arnow reagent (Hydroxmate) and Csaky method (Catecholate). The supernatant turned pink upon addition of ferric perchlorate indicating the hydroxmate group of siderophore. Quantitative estimation showed that the organism produced a maximum of about 1000 µg mL-1 of hydroxamate type of siderophore in culture medium (Table 1) after 24h of incubation which remained constant even after 30 h of incubation. The pH of the media changes as the culture ages and uses up the available nutrients. Siderophore production also increases as iron is depleted from the media. Therefore increase in pH may be coincidental to increase in siderophore concentration. The pH increased from 6.8 to a maximum of 10 along with siderophore production. It is reported that alkaluine pH helps in solubilization of iron which results into more iron content in medium and hence a decline in siderophore production (7). This change in pH of the medium during siderophore production was also reported by Budzikiewicz (16) mentioning that alkalinity is important to avoid siderophore destruction. On the contrary Sharma and Johri (17) showed that higher pH is rather destructive to siderophores.
Effect of different FeCl3 concentration on siderophore production
Pseudomonas showed increase in growth with increase in FeCl3 concentration revealing that presence of FeCl3 is vital for its growth (Figure 3) .This was also reported by De Villegas (17) who stated that concentration of FeCl3 above 10 µM has a negative effect on siderophore production whereas Manninen and Sandholm (19) reports that highest siderophore production occurs only at iron concentration at and above 50 µgmL-1. Our results show maximum siderophore production occurs at 2 µM FeCl3 which declines thereafter up to 20 µM of Fe. An increase in fluorescence was reported along with increase in FeCl3 concentration up to 2 mM FeCl3 concentration. It can be reported that production of fluorescence is a response to presence or absence of FeCl3 in the medium. Amount of fluorescence produced by the isolate Pseudomonas increased along with the concentration of FeCl3 but up to just 2 mM concentration after which a continuous decrease was reported (Figure 3). This increase was parallel to growth of the isolate, which shows that pyoverdin biosynthetic genes and thereby fluorescence are under the control of iron regulated promoters.
Extraction and purification of siderophore crystals from the supernatant
Extraction of ferrichrome type of hydroxamates by Benzyl alcohol method yielded fine needle shaped crystals after entire process. These crystals were then collected and studied for FTIR analysis on KBr pellets range between the ranges of 2.5 to 14 (4000-400 cm-1). This scale was selected according to PBHA crystals used as standard. FTIR results (Figure 4) show that the crystals obtained had hydroxamate functional group, which correlated with the peaks obtained from the FTIR analysis of PBHA crystals. Peaks were observed at 3189, 2360, 1602, 1566, 780 and 530 wave number, which are same as those obtained from PBHA crystals FTIR analysis. But along with these peaks two more peaks were also observed at 1495 and 1105 wave number revealing the presence of one -C-H bending with functional group -CH2 and one -N-O structure due to functional group N-O bonding, which shows that although these are hydroxamate crystals they still contain other functional groups, which were not observed in FTIR analysis of standard hydroxamic acid crystals. There are reports that hydroxamate crystals of fungal siderophore contained functional groups like methyle, amide, secondary amine, methylene, N-O bond and a ring structure (M-O) where M=Fe (12). As observed in the present study, the certain functional chemical group resembled ferrichrome siderophores.
The absorption spectra of the pyoverdin extracted were found to be pH sensitive. At lower pH (3.0-5.0) the peaks were found at 385 nm where as at pH 7.0, the major peak was found to be at 410 nm (Figure 5). Similar results were also quoted by Xiao (18) who reported that atypical pyoverdins had double peaks at low pH values (i.e. 366 & 384 nm for Pf-A, 368 & 384 for Pf-B and 369 and 385 nm for Pf-C). However at higher pH values (pH 7), the pyoverdin spectra had single peaks (407 nm for Pf-A and Pf-B where as Pf-C has a peak at 408 nm on UV spectra. Bultreys et al (5) report that as the pH of the supernatant containing pyoverdin is reduced, the absorption maxima moves towards the lower ultra-violet range. According to him, P. asplenii shows absorption maxima at pH 7.0 at about 407 nm, which became 406 nm at pH 4.0 and 405 nm at pH 3.5. Thus it behaves as putative pyoverdin at lower pH (3.0) and as distinctive pyoverdin as the pH increased from 3.0 to 7.0 and above. All pyoverdins have a common feature in its molecular structure i.e. a constant quinoline chromophore group bound to a peptide chain and to a dicarboxylic acid or a dicarboxylic amide (21). and the presence of three iron-binding ligands. One ligand is located in a catechol chain and one on hydroxamic acid chain derived from ornithin or b-hydroxyaspartic acid. The atypical feature of the pyoverdin of P. syringae and P. viridflavia is the presence of two OH-Asp residues of Ornithin in the chelation of iron. This feature influences the spectral characteristics of Fe(III) chelated atypical pyoverdin (14). The main difference observed between siderophores produced by different Pseudomonas is the arrangement of L and D amino acids. Pyoverdins can be further segregated as typical and atypical pyoverdins.
Detection and Comparision of Pyoverdins by HPLC and ESIMS
Dominant peak for this pyoverdin appeared at 14.906 min, 16.975 min and 18.444 min (Fig: 6). RT data allowed discrimination between pyoverdin with different peptide chains produced by different species of Pseudomonas (5). In visual tests a change in color of production medium that accompanied in the pH 7.0 to 4.0 indicated atypical pyoverdin production(14). Reference strain P. syringae B301D δRT of 18.783 min and P. chicorii LMG 2162 RT of 19.075 min, P. syringae pv. syringae PSP1 with RT of 18.758 min. Two smaller peaks at 17.922 min and 18.444 min were obtained in our sample. These other peaks could be correlated to minor peaks found in P. fuscovaginae (14.906 and 16.975 min). The result obtained with HPLC chromatogram reveals the ∆RT of 0.070 with distinguished HPLC of P. syringae LMG13190 and ∆RT of 0.341 with standard HPLC of P. cichorii LMG showing presence of Pa A type of atypical pyoverdine.
As the pyoverdin profiles obtained were complex, the dominant pyoverdins of the reference strains as reported by Fuch and Budzekiewicz (22) were used for comparisons. ESIMS when performed using purified supernatant of the culture, yielded several peaks as mentioned in the Table 2. The peaks were obtained in a wide range of m/z starting from 399 m/z to1239 m/z. The peak at 399 m/z represents presence of A1 fragment with a loss of one H2O molecule. Next visible peak was at 417 m/z which represent A1 fragment showing presence of succinic acid side chain. Peak 445 m/z shows presence of serine where as 504 shows B5S-H2O fragment representing Thr-AhO-Ala-Ly-Ser side chain. Peak at 575 m/z shows present of Lys-Ser fragment. The highest peak observed was at 717 m/z showing presence of Y6" fragment of pyoverdin. This side chain contains amino acids like Ala-Thre-Oho-Ala-Ly-Ser in sequence. Peak at 1067 m/z shows loss of succinic acid from pyoverdin of P. fluorescens showing molecular mass of 1167 m/z as reported (23). The result also shows that the siderophore contains C terminal with OHOrn side chain. Peaks at 1105 m/z represent side chain with Asp-Lys-OHasp-Ser-Ala-Ser-cOHOrn. Peak at 1123 m/z shows presence of CH3CHO+Thr and a peak at 1187 m/z represents a side chain of Ser-Dab-Gly-Ser_OHasp-Ala-Gly-Ala_Gly-cOHOrn. Peak at 1149 m/z reperesents a loss of H2O molecule from the previous peak 1167 m/z visible in the spectra. Certain peaks i.e 1149 m/z and1167 m/z showed a gradual loss of H2O molecule from the actual molecule 1187 which resembles the presence of amino acid side chain Ser-Dab-Gly-Ser-OHasp-Ala-Gly-Ala-Gly-cOHOrn (Table 2). Siderophores like pyoverdins produced by the fluorescent members of the bacterial genus are very complex in structures. Their peptidic part- linear or partially cyclic-comprises unusual and partially modified amino acids which makes their interpretation difficult. Free pyoverdins as well as the ferri pyoverdins generally give abundant [M+H]+ ions occasionally accompanied by [M+2H]+2 with lower intensity as is observed over here at 774 m/z peak where as peak at 557 m/z represent [M+2H] with a loss of CO and H2O molecules(22). Most important is the formation of fragment A1 which has been observed in all pyoverdins showing presence of succinic acid side chain with Ser as first amino acid. Present report also show a peak at 417 m/z which represent the presence of fragment A1 containing Ser as first amino acid in the side chain which supports that the siderophore extract contains pyoverdin type of siderophores. The obtained ESIMS spectrum resembles the ESI spectrum of P. fluorescens P19 pyoverdin obtained by Fuch and Budzekiewicz, (22) where they mention that ESI of [M+H]+ of pyoverdin shows a peak at 1169 m/z reporting that OH transfer is possible from other amino acids (Asp, Fho, Ser etc). The present pyoverdin contains cOHOrn C-terminal resembling the peptide chain of Py 2798. Here cyclic chain is if Ser/Dab which refers to the condensation product of the Γ- NH2 group of Dab with the amide carbonyl group of the preceding amino acid giving a tetrahydro pyrimide ring as mentioned by Fuchs and Budzekiewicz (22).
Pseudomonas have been studied widely as siderophore producers and siderotyping is an important step in identification of Pseudomonas as it is species specific. The novel isolate Pseudomonas fluorescens shows some distinct features which have not been observed so far in and suggests a new type of Pyoverdin.
We sincerely acknowledge the funding facilities from the University Grant Commission (UGC) India to conduct these studies. Thanks are due to Prof..S K Menon, Department of Chemistry for helping us in sample analysis and interpretation of results.
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Submitted: April 05, 2011
Returned to authors for corrections: July 27, 2011
Approved: January 16, 2012
* Corresponding Author. Mailing address: Department of Microbiology, University School of Sciences, Gujarat University of Sciences, Gujarat University, Ahmedabad 380 009, Gujarat, India.; Tel.: 079-26503225.; E-mail: email@example.com