A simple and efficient method for poly-3-hydroxybutyrate quantification in diazotrophic bacteria within 5 minutes using flow cytometry

Abstract

The conventional method for quantification of polyhydroxyalkanoates based on whole-cell methanolysis and gas chromatography (GC) is laborious and time-consuming. In this work, a method based on flow cytometry of Nile red stained bacterial cells was established to quantify poly-3-hydroxybutyrate (PHB) production by the diazotrophic and plant-associated bacteria, Herbaspirillum seropedicae and Azospirillum brasilense. The method consists of three steps: i) cell permeabilization, ii) Nile red staining, and iii) analysis by flow cytometry. The method was optimized step-by-step and can be carried out in less than 5 min. The final results indicated a high correlation coefficient (R²=0.99) compared to a standard method based on methanolysis and GC. This method was successfully applied to the quantification of PHB in epiphytic bacteria isolated from rice roots.

Flow cytometry; Nile red; Poly-3-hydroxybutyrate; Herbaspirillum seropedicae; Azospirillum brasilense

Introduction

Polyhydroxyalkanoates (PHAs) are biodegradable polymers that can provide an environmentally friendly alternative to replace petroleum-based plastics (¹). Poly-3-hydroxybutyrate (PHB) is the most abundant naturally-occurring polyester produced by bacteria in response to carbon oversupply and other nutrient limitations, such as low nitrogen levels (²). PHB is stored as cytoplasmic granules with a diameter ranging from 0.2 to 0.5 µm, and can provide carbon and energy for the bacteria under certain conditions (³).

The initial studies concerning PHAs detection were based on gravimetric and infrared spectroscopy methods, and the earliest research in PHB quantification was performed using gas chromatography (GC) (³). Although several methods have been described for this purpose, such as HPLC (⁴), fluorescent dyes (⁵), ionic chromatography, and enzymatic methods (⁶), GC is still the preferred standard method for PHB quantification, showing high sensitivity, accuracy, and reproducibility. However, there are three major drawbacks associated with GC-based methods: i) the use of hazardous solvents at high temperature, ii) a long time requirement for sample processing, and iii) the need for large amounts of bacterial cells. Thus, there is a need for alternatives to GC for PHB quantification.

In the early 1980's, Nile red [9-diethylamino-5H-benzo(α)phenoxazine-5-one] was described as a promising fluorescent dye for detection of intracellular lipid droplets by flow cytometry in aortic smooth muscle cells and on cultured peritoneal macrophages (⁷). In the 1990's, a method based on Nile red (NR) staining was applied for the detection of PHB production in Alcaligenes eutrophus (⁸) and Ralstonia eutropha H16 (⁵). To date, several protocols established for NR staining and PHB quantification by flow cytometry in Saccharomyces cerevisae, Cupriavidus necator (⁹), Synechocystis sp. strain PCC6803, Escherichia coli (¹⁰), and three Pseudomonas sp. (¹¹) have been reported. The optimization of a flow cytometry protocol for the quantification of PHB requires the determination of conditions for efficient cell permeabilization and optimal NR concentration, parameters that are dependent on cell type, membrane properties and bacterium size.

Herbaspirillum seropedicae and Azospirillum brasilense are plant growthpromoting diazotrophic bacteria (¹²,¹³). While there are several indications that PHB plays important roles in nitrogen fixation and plant-bacteria interactions (¹⁴ –¹⁷), the real significance of PHB for bacteria during plant-colonization remains unknown. The development of techniques allowing PHB quantification in small volumes and low cell numbers will allow data collection in restrictive conditions – such as in bacteria colonizing roots and other plant tissues – and will contribute to the determination of the true role of PHB in plant-bacteria association. In this study, we describe the optimization and validation of a simple, fast and accurate method for the quantification of PHB production in H. seropedicae and A. brasilense, based on NR staining and flow cytometry.

Material and Methods

Reagents and buffers

Phosphate-buffered saline (PBS) containing 137 mM NaCl, 2.7 mM KCl, 8 mM Na₂HPO₄ and 1.4 mM KH₂PO₄ at pH 7.2 NR (Sigma Aldrich, USA) was dissolved in DMSO to a final concentration of 3.14 mM (1 mg/mL) and kept in the dark. NR was further diluted in different buffers as indicated in the Figure legends. TBAC buffer [PBS containing 1 mM EDTA and 0.01% (v/v) Tween 20] was used to avoid the formation of bacterial aggregates that could potentially perturb light-scattering and fluorescence signals in flow cytometric analysis. TSE buffer contains 10 mM Tris-HCl pH 7.5, 20% (wt/vol) sucrose and 2.5 mM EDTA. All other reagents were commercial products of the highest purity grade available.

Bacterial strains and growth conditions

H. seropedicae strain SmR1 (wild type) (¹⁸) and strain ΔphaC1, an SmR1 mutant deficient in PHB synthesis, previously described as ΔphbC1 (¹⁹), were cultivated in NFbHP-malate medium containing 0.5% of DL-malic acid and 20 or 5 mM of NH₄Cl. A. brasilense strain FP2 (²⁰) and A. brasilense Sp7 mutant strain phbC (²¹) were cultivated in NFbHP-lactate medium containing 0.5% of DL-lactic acid and 20 or 5 mM of NH₄Cl. A. brasilense FP2 is a spontaneous mutant strain from A. brasilense Sp7 resistant to nalidixic acid and streptomycin (²⁰). Antibiotics were added to the growth media in the following concentrations: streptomycin (80 µg/mL) for H. seropedicae, streptomycin (80 µg/mL) and nalidixic acid (10 µg/mL) for A. brasilense strain FP2, and kanamycin (100 µg/mL) for A. brasilense Sp7 mutant strain phbC.

PHB quantification by gas chromatography

The bacterial PHB amount was determined by acid methanolysis followed by GC coupled to a flame-ionization detector as previously described (²²). Methanolysis was performed with 5–10 mg of lyophilized bacteria in 2 mL of chloroform and 2 mL of methanol containing 15% sulphuric acid in borosilicate glass tubes with screw caps. For each reaction, 0.5 mg of benzoic acid was added as internal standard. Reaction mixtures were incubated at 100°C for 3.5 h in a dry-heating block. After cooling, 1 mL of distilled water was added and the tubes were vortexed for 60 s. The upper aqueous phase was removed and the lower organic phase containing the resulting 3-hydroxybutyric methyl ester (Me-3-HB) was dried with Na₂SO₄ and analyzed by GC in a 450 GC chromatograph (Varian, Netherlands) equipped with a CP-Sil-5 CB column (10 m×0.53 mm ID). Argon was used as carrier gas at 0.9 mL/min. The injector was set at 250°C and the detector at 275°C. The oven temperature program was: initial temperature 50°C for 2 min, then from 50°C up to 110°C at a rate of 20°C/min and finally up to 250°C at a rate of 20°C/min. The PHB amount in each sample was normalized by the weight of the lyophilized bacteria and expressed as a percentage of PHB/cell dry weight.

PHB quantification by flow cytometry

Flow cytometry experiments were performed in a BD Accuri C5^® Flow Cytometer (USA) equipped with a 488-nm laser for fluorescence excitation. For each sample, 100,000 events were acquired, and the median fluorescence intensities were obtained from histograms of FL2-H 585/40 nm channel. Flow cytometry calibration was performed using spherothech 8-peak beads (BD Accuri^™, USA) according to the manufacturer's recommendations and instructions.

Optimization of the flow cytometric protocol for PHB quantification

For all steps of the optimization process, an aliquot of 100 µL (∼10⁶–10⁷ cells/mL) of the cell culture was centrifuged for 1 min at 13,400 g at room temperature, the supernatant solution was discarded and the cell pellet was treated according to each specific condition. For all conditions, after staining with NR, the cells were collected by centrifugation for 1 min at 13,400 g and resuspended in TBAC buffer for analysis by flow cytometry. During the optimization process the following steps were carried out in order of description:

1. Cell permeabilization conditions: the cell pellet was resuspended in 1 mL of each of the evaluated membrane permeabilization solutions (TBAC containing 30% of ethanol, TBAC containing 0.1% of Triton X-100 and TSE buffer). The bacterial suspensions were stained with NR (9.42 µM) for 5 min and analyzed by flow cytometry.

2. Optimization of the ethanol concentration for cell permeabilization: the cell pellet was resuspended in 1 mL of TBAC buffer containing increasing concentrations of ethanol (up to 70%). After 5 min of ethanol exposure, cells were stained with NR (9.42 µM) for 5 min.

3. Bacterial cell permeabilization time: the cell pellet was resuspended in 1 mL of TBAC buffer containing 50% of ethanol and incubated up to 30 min. After ethanol exposure, cells were stained with NR (9.42 µM) for 5 min.

4. Optimization of NR staining: the cell pellet was resuspended in 1 mL of TBAC buffer containing 50% of ethanol for 1 min. After ethanol exposure, cells were stained with NR (9.42 µM) for up to 30 min.

5. Determination of the optimal NR concentration: the cell pellet was resuspended in 1 mL of TBAC buffer containing 50% of ethanol for 1 min. After ethanol exposure, cells were stained with NR (0 to 500 µM) for 1 min.

6. Fluorescence stability: the cell pellet was resuspended in 1 mL of TBAC buffer containing 50% of ethanol for 1 min. Cells were subsequently stained with NR (31.25 µM) for 1 min, centrifuged (1 min at 13,400 g), and resuspended in TBAC buffer for analysis by flow cytometry. The NR fluorescence was monitored during 90 min by flow cytometry. In addition, samples were stored at 4°C in permeabilization solution (TBAC buffer containing 50% of EtOH), until analysis.

PHB quantification by flow cytometry using NR fluorescence

The optimized protocol for the quantification of PHB by flow cytometry is described as follows: an aliquot of 100 µL (∼10⁶–10⁷ cells/mL) of a bacterial culture is centrifuged for 1 min at 13,400 g. The supernatant solution is discarded and the cell pellet is resuspended in 1 mL of TBAC containing 50% of ethanol. After 1 min of incubation, samples are stained with 31.25 µM of NR for 1 min in the dark, centrifuged 1 min at 13,400 g, and the supernatant solution discarded. The pellet is then resuspended in 1 mL of TBAC solution and immediately analyzed by flow cytometry.

PHB staining for fluorescence microscopy

The same optimized protocol to prepare bacterial cells stained with NR for flow cytometry was applied to prepare cells for fluorescence microscopy. The non-optimized protocol (⁹) differed from the optimized one mainly in the ethanol (30%) and NR concentration (9.42 µM). The fluorescent images were obtained using the Axio Imager Z2 microscope (Carl Zeiss, USA), equipped with the scanning platform Metafer 4 and CoolCube 1 camera (Metasystems, USA) magnifying 100 times.

PHB production by epiphytic rice bacteria

Rice experiments were performed according to Valdameri et al. (²³). PHB measurements in the epiphytic bacterial populations were performed in bacteria detached from plants 7 days after inoculation. Bacteria were removed from roots by vortexing for 1 min in 1 mL of TBAC containing 50% of ethanol. The suspension was stained with NR following the optimized protocol.

Results

Screening for permeabilization solutions

To determine the best cell permeabilization solution to stain H. seropedicae strain SmR1 and A. brasilense strain FP2 with NR, we initially compared three different conditions: i) TBAC containing 30% of ethanol, ii) TBAC containing 0.1% of Triton X-100, and iii) TSE buffer. TBAC buffer was previously applied to determine bacterial cell concentration by flow cytometry (²³).

As shown in Figure 1A and B, intracellular fluorescence of samples stained with NR in TBAC (TBAC+) or TBAC containing detergent (0.1% triton X-100), did not differ from non-stained (TBAC-) samples. In addition, a sucrose-buffer (TSE) produced only a partial permeabilization effect. The representative histograms of A. brasilense strain FP2 permeabilized with TSE buffer clearly showed a heterogeneous cell population (Figure 1A). The same heterogeneous distribution was observed with the H. seropedicae strain SmR1 treated with TSE buffer (data not shown). TBAC buffer containing 30% of ethanol (EtOH) permeabilized both H. seropedicae strain SmR1 and A. brasilense strain FP2, producing a single peak of higher fluorescence, denoting a homogeneous and full membrane permeabilization.

Figure 1
Screening for cell permeabilization solutions. Bacteria were grown at an OD₆₀₀ of 1.2, 0.1 mL was centrifuged (1 min at 13,400 g), and resuspended in 1 mL of each solution evaluated. The bacterial suspensions were stained with NR (9.42 µM) during 5 min, and analyzed by flow cytometry. A, Histograms are representative of A. brasilense strain FP2. Conditions: TBAC- corresponds to Nile red (NR) non-stained samples, used as a blank. All other samples were stained with NR. TBAC+ corresponds to non-permeabilized samples in TBAC. EtOH 30% corresponds to samples in TBAC containing 30% of ethanol. Triton 0.1% corresponds to samples in TBAC containing 0.1% of Triton X-100. TSE corresponds to samples in TSE buffer. TSE/EtOH 30% corresponds to overlay of two histograms, TSE and EtOH 30%, respectively. B, Fluorescence data (arbitrary units, a.u.) are reported as means±SD of 3 independent experiments with H. seropedicae strain SmR1 and A. brasilense strain FP2, by using the median fluorescence intensity values in the FL2-H channel.

Optimization of ethanol percentage for cell permeabilization

Since TBAC buffer containing 30% of ethanol permeabilized both bacteria, the effect of ethanol concentration on NR staining was evaluated. Fluorescence histograms of A. brasilense strain FP2 reveal that an increase in ethanol concentration increased the amount of permeabilized cells. Indeed, for both bacteria, TBAC buffer containing 50% of ethanol was the best condition for permeabilization considering the increase in NR fluorescence, and a single distinct peak (Figure 2A and B).

Figure 2
Optimization of ethanol (EtOH) percentage in TBAC buffer for cell permeabilization. Bacteria were grown at an OD₆₀₀ of 1.2, 0.1 mL was centrifuged (1 min at 13,400 g), and resuspended in 1 mL of TBAC buffer containing different percentages of EtOH (0-70%). After 5 min of EtOH exposure, cells were stained with Nile red (9.42 µM) during 5 min, centrifuged (1 min at 13,400 g), and resuspended in TBAC buffer for analysis by flow cytometry. A, Histograms are representative of A. brasilense strain FP2 using different percentages of EtOH in TBAC buffer, as indicated. B, Fluorescence data (arbitrary units, a.u.) are reported as means±SD of 3 independent experiments with H. seropedicae strain SmR1 and A. brasilense strain FP2, by using the median fluorescence intensity values in the FL2-H channel.

Permeabilization time, Nile red exposure and optimal concentration

Cells were incubated in TBAC buffer containing 50% of ethanol up to 30 min before NR staining. As shown in Figure 3A, NR fluorescence levels were similar regardless the incubation time. Therefore, 1 min of permeabilization was used in further experiments, allowing the manipulation of five samples simultaneously. A range of NR incubation periods from 0 to 30 min was also evaluated, and the results showed a similar pattern observed previously for the permeabilization time experiments, with no significant variation in fluorescence values for all sampling times (Figure 3B). Based on these results, the NR time exposure was established as 1 min. It is noteworthy that both H. seropedicae strain SmR1 and A. brasilense strain FP2 showed the same behavior, allowing the use of the same protocol for both species.

Figure 3
Incubation time required for cell permeabilization and Nile red (NR) staining. Bacteria were grown at an OD₆₀₀ of 1.2, 0.1 mL was centrifuged (1 min at 13,400 g), and resuspended in 1 mL of TBAC buffer containing 50% of EtOH. A, Exposure with EtOH during 0 to 30 min and cells stained with NR (9.42 µM). B, After 1 min of exposure in TBAC buffer containing 50% of EtOH, the bacterial suspensions were incubated with NR (9.42 µM) during 0 to 30 min. C, After 1 min of exposure of cells in TBAC buffer containing 50% of EtOH, the bacterial suspensions were stained with NR (0 to 500 µM) during 1 min, centrifuged (1 min at 13,400 g), and resuspended in TBAC buffer for analysis by flow cytometry. Fluorescence data (arbitrary units, a.u.) are reported as means±SD of 3 independent experiments with H. seropedicae strain SmR1 and A. brasilense strain FP2, by using the median fluorescence intensity values in the FL2-H channel. D, Histogram overlay of three samples, a mutant strain of H. seropedicae, ΔphaC1, H. seropedicae strain SmR1, and A. brasilense strain FP2, using the optimized concentration of NR (31.25 µM).

To determine the optimal NR concentration to stain cells with higher fluorescence values, a range from 0 to 500 µM was assayed. Since NR is not a PHB-specific dye, it was necessary to measure the NR fluorescence background in non-PHB producing cells. The H. seropedicae SmR1 derived mutant ΔphaC1 defective in PHB production was tested against the wild type SmR1, both at OD₆₀₀ 1.2. For A. brasilense strain FP2, the wild type at low (0.3) and high (1.2) OD₆₀₀ were compared. These conditions were selected based on our GC data (not shown) that have shown a high production of PHB at OD₆₀₀ 1.2 for both wild type strains, whereas both H. seropedicae ΔphaC1 mutant strain and A. brasilense strain FP2 at OD₆₀₀ 0.3 did not produce PHB, as detected by the GC method. The optimal NR concentration was 31.25 µM for both bacteria (Figure 3C and D).

Fluorescence emission stability

The last parameter to be optimized was the NR fluorescence stability in TBAC buffer and in non-stained and stored permeabilized samples. The fluorescence emission stability of NR stained samples of A. brasilense strain FP2 was monitored for a duration of 90 min (Figure 4A). The NR fluorescence started to decrease 5 min after staining. After 30 min, the fluorescence levels were similar to those of the background level. However, it is worth noting that unstained permeabilized cells can be stored under refrigeration (2 to 8°C) without significant loss of NR staining capacity for up to 5 days (Figure 4B). Therefore, one can store samples prior to NR staining for up to 5 days and then stain cells and capture the emitted fluorescence.

Figure 4
Nile red (NR) fluorescence stability. A. brasilense strain FP2 was grown until reaching OD₆₀₀ of 1.4. PHB measurements were performed using the optimized procedure, as described in the Materials and Methods. A, After resuspension of cells in TBAC buffer, NR fluorescence was monitored during 90 min by flow cytometry. B, Samples were stored at 4°C in permeabilization solution (TBAC buffer containing 50% of EtOH), until analysis, as indicated. For analysis, samples were stained with NR (31.25 µM) during 1 min, centrifuged (1 min at 13,400 g), resuspended in TBAC buffer and analyzed immediately by flow cytometry. Fluorescence data (arbitrary units, a.u.) are reported as means±SD of 3 independent experiments with H. seropedicae strain SmR1 and A. brasilense strain FP2, by using the median fluorescence intensity values in the FL2-H channel.

Flow cytometry versus gas chromatography

Several reports have demonstrated a linear correlation between the amount of PHB and the fluorescence emission intensity of NR stained cells. In order to validate the optimized method for PHB quantification by flow cytometry, the standard gas chromatography method was applied to the same bacterial cultures. H. seropedicae SmR1 and ΔphaC1 strains, A. brasilense strain FP2, and mutant of A. brasilense strain Sp7, identified as phbC Sp7, impaired in the production of PHB, were grown in a medium containing 5 and 20 mM NH₄Cl, since PHB production has been correlated with carbon availability and nitrogen limitation.

The results revealed that the kinetic curves of NR fluorescence as a function of OD₆₀₀ varied among bacteria. As shown in Figure 5A, H. seropedicae strain SmR1 grown in 5 mM NH₄Cl produced more PHB as compared to the growth in 20 mM NH₄Cl, results also confirmed by GC. For A. brasilense strain FP2, low NH₄Cl levels also triggered PHB production; however, A. brasilense strain FP2 grown in 20 mM NH₄Cl did not produce any detectable PHB (results also confirmed by GC; Figure 5B). These data highlighted important differences between PHB accumulation in H. seropedicae strain SmR1 and A. brasilense strain FP2, since H. seropedicae strain SmR1 seems to always produce PHB, even at low OD₆₀₀, whereas A. brasilense strain FP2 produces PHB only in OD₆₀₀ 1.0 or higher, with limiting nitrogen concentration in the growth medium. As shown in Figure 5C, flow cytometry and GC present a very high correlation coefficient (R²) of 0.99 for both bacteria.

Figure 5
Correlation between flow cytometry and gas chromatography (GC) analysis for PHB quantification. PHB measurements by flow cytometry using the optimized procedure and the standard method based on GC were applied on H. seropedicae strain SmR1, a mutant strain of H. seropedicae, ΔphaC1, A. brasilense strain FP2, and a mutant strain of A. brasilense, phbC SP7, OD₆₀₀ ranging from 0.6 to 1.4 using two NH₄Cl concentrations in growth medium, as indicated. A, H. seropedicae. B, A. brasilense. C, Correlation between flow cytometry and GC. Fluorescence data (arbitrary units, a.u.) are reported as means±SD of 3 independent experiments with H. seropedicae strain SmR1 and A. brasilense strain FP2, by using the median fluorescence intensity values in the FL2-H channel.

Fluorescence microscopy analysis

Although this method has been optimized with every precaution possible to ensure high accuracy in flow cytometry determination of PHB, the same protocol can be successfully applied to stain cells for fluorescence microscopy analysis. To confirm this assumption, H. seropedicae and A. brasilense samples stained with NR using the optimized protocol were analyzed by fluorescence microscopy. In addition, the non-optimized versus optimized procedures were compared. Fluorescent micrographs of H. seropedicae and A. brasilense revealed an increase fluorescence emission intensity in samples stained using the optimized protocol (Figure 6).

Figure 6
Intracellular PHB detection by fluorescence microscopy using the non-optimized and optimized protocols. H. seropedicae strain SmR1, a mutant strain of H. seropedicae, ΔphaC1, A. brasilense strain FP2, and a mutant strain of A. brasilense, phbC SP7 were grown to OD₆₀₀ of 1.4 using 5 mM NH₄Cl in growth medium. Fluorescence microscopy analysis was performed using the procedure described in the Material and Methods.

PHB production in epiphytic bacteria analyzed by flow cytometry

To determine whether this optimized method could be applied to quantify PHB in small-cell-number samples, H. seropedicae strain SmR1 and A. brasilense strain FP2 cells epiphytically growing on rice roots were detached, stained and PHB was quantified by flow cytometry. After 7 days of rice inoculation, the results showed that both H. seropedicae SmR1 and A. brasilense FP2 grown epiphytically on rice produced PHB during colonization (Figure 7). This is a first-time demonstration of what can be considered an easy and reliable approach to follow the kinetics of PHB production by epiphytic bacteria. Since the amount of epiphytic cells is usually insufficient to be determined by GC-based methods, the optimized protocol developed in the present work constitutes an important tool to monitor the production of PHB during plant-bacteria interaction, to screen for potential PHB producers among plant-associated bacteria, and in biotechnological studies to evaluate and improve PHB production by bacteria.

Figure 7
PHB production of epiphytic bacteria analyzed by flow cytometry. PHB measurements were performed using the optimized procedure on rice epiphytic H. seropedicae strain SmR1, a mutant strain of H. seropedicae, ΔphaC1, A. brasilense strain FP2, and a mutant strain of A. brasilense, phbC SP7, 7 days after inoculation, as described in the Material and Methods. Fluorescence ratio data are reported as means±SD of 2 independent experiments performed in triplicate, using the median fluorescence intensity values in the FL2-H channel.

Discussion

For the feasibility of a NR-based method, the dye must cross the bacterial membranes in order to stain the intracellular PHB. Full uptake of fluorescent dyes appears to be critical for a complete intracellular target staining. Besides the hydrophobicity of NR, the bacterial uptake varies widely among different species, essentially due to differences in membrane permeability. Several strategies can be applied to improve the entry of NR, such as those using buffers containing ethanol (⁹), or sucrose-based buffers, such as the TSE buffer (¹⁰).

The sucrose-buffer TSE was successfully applied to permeabilize cells of Synechocystis sp. PCC6803 and Escherichia coli to NR staining in PHB-producing conditions (¹⁰). In the present work the TSE buffer failed to efficiently permeabilize H. seropedicae strain SmR1, and produced only a partial effect on A. brasilense strain FP2 (Figure 1A and B). The TBAC buffer, on the other hand, containing 50% ethanol was found to be the best permeabilization solution for H. seropedicae and A. brasilense.

Apparently, the optimal NR concentration can vary among species, and therefore the adjustment of the concentration according to species is a critical step for optimization. For both H. seropedicae and A. brasilense strains, fluorescence emission increased up to the NR concentration of 31.25 µM, decreasing at higher concentrations of NR (Figure 4A). Despite the very low concentration of NR (0.032 µM) described for both Saccharomyces cerevisae and Cupriavidus necator (⁹), most bacteria require higher NR concentrations, as demonstrated for Synechocystis sp. strain PCC6803 (3.3 µg/mL – 9.42 µM), Escherichia coli (33 µg/mL – 94.2 µM) (¹⁰) and Ralstonia pickettii AR1 (20 µg/mL – 62.8 µM) (²⁴). Such variations clearly show that protocols must be optimized for each microbe under study before the introduction of NR-fluorescence flow cytometry as a technique to quantify PHB or other kinds of neutral lipids.

Compared to H. seropedicae strain SmR1, in all conditions assayed here, A. brasilense strain FP2 always produced higher basal fluorescence values (Figures 2, 3, and 5). Two major reasons could explain this observation: i) NR binding to different intracellular lipid droplets, and ii) the difference in size between the H. seropedicae strain SmR1 and A. brasilense strain FP2, which is almost twice the size. In view of this, we hypothesize that the higher fluorescence emission values observed for A. brasilense strain FP2 are probably due to the bacteria size.

Despite the fact that PHA quantification by GC is largely used in microbial PHA research, this methodology is quite laborious and requires hazardous solvent manipulations. The standard method for PHB quantification involving methanolysis followed by GC analysis is a well-established and reproducible technique, however with a main drawback: the long time needed to analyze sample by sample. A typical procedure of methanolysis followed by GC analysis requires 16 h of lyophilization, 5 h of methanolysis and 20 min for GC data acquisition for each sample – at least 250 times longer than our NR optimized protocol using flow cytometry, which was less than 5 min. In addition, our flow cytometry protocol is even faster than other flow cytometry methodologies that require 25 to 50 min to be completed (⁹,¹⁰,²⁴). Another advantage of the NR flow cytometry protocol reported here is the low amount of cells required for analysis, which unlike other methodologies allows one to perform a larger number of experiments in different conditions. While the quantification of other PHAs, such as polyhydroxyhexanoate and polyhydroxyoctanoate, was not tested in this study, we believe our protocol can be successfully adapted to quantify other PHAs.

The methodologies used here, flow cytometry and GC, applied to PHB quantification presented a very high correlation coefficient (R²) of 0.99 for both bacteria. This level of correlation is in agreement with methods optimized for other microorganisms, such as E. coli (R²=0.96) (¹⁰), S. cerevisiae (R²=0.99), and C. necator (R²=0.99) (⁹).

In summary, a reliable and relatively fast flow cytometric procedure was developed for PHB quantification in H. seropedicae SmR1 and A. brasilense FP2 grown in cultures or in cells isolated from grass root surfaces. PHB production can be quantified with accuracy and precision using NR staining, following the six optimized steps detailed in this paper. This protocol has potential to be used in other studies involving PHB metabolism in these and other bacterial species, as well as in quality control of inoculant, since PHB production has been reported as an important feature to maintain the fitness of plant-associated bacteria.

Acknowledgments

We thank Roseli Prado, Valter Baura and Marilza Doroti Lamour for technical assistance and Dr. Gladys Alexandre, University of Tennessee, for providing the Azospirillum brasilense SP7 mutant strain phbC. We are also grateful for the National Institute of Science and Technology of Nitrogen Fixation INCT/CNPq/MCT and CAPES for financial support. G. Valdameri thanks PNPD/CAPES for a postdoctoral scholarship.

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Publication Dates

• Publication in this collection
  2017

History

• Received
  17 June 2016
• Accepted
  26 Sept 2016