Method of synthesizing biogenic elemental selenium nanostructure using enterobacter cloacae and application thereof

Abstract

A method of synthesizing biogenic elemental selenium nanostructure using Enterobacter cloacae and its application. The method uses E. cloacae Z0206 to reduce selenite to zero valence selenium and forms nano-sized elemental selenium particles, including steps of inoculating activated E. cloacae Z0206 to fermentation broth, adding sodium selenite solution, shaking and incubating, collecting the fermentation broth and separating the elemental selenium nanoparticles.

Claims

1. A method of synthesizing biogenic elemental selenium nanoparticles using selenite as starting materials and Enterobacter. cloacae Z0206, which is deposited in China General Microbiological Culture Collection Center (CGMCC) on Dec. 3, 2007 with a CGMCC depository No. 2279, as fermentative bacteria, comprising the steps of: inoculating activated Enterobacter. cloacae Z0206 cells to a fermentation broth containing potassium phosphate, and adding sodium selenite solution to obtain an inoculated broth, wherein the final concentration of sodium selenite in the fermentation broth is 10 mM; shaking and incubating the inoculated broth to obtain a fermented broth, wherein the temperature, rotation speed and incubation time during shaking and incubating step are 32 C., 250 rpm and 144 hours, respectively; and collecting the fermented broth, performing a first centrifugation on the fermented broth to obtain a supernatant, performing a second centrifugation on the supernatant to obtain a sediment, re-suspending the sediment with double distilled water to obtain a suspension, ultrasonicating the suspension, adding hexane to the suspension, and mixing and stratifying the suspension by standing to result in a lower red aqueous phase, wherein the biogenic elemental selenium nanostructures should present in the lower red aqueous phase, wherein parameters of the first centrifugation are 4 C., 5,000g, 15 minutes, parameters of the second centrifugation are 4 C., 25,000g, 15 minutes, parameters of the ultrasonication are 25 W, 5 seconds on and 5 seconds off for 15 minutes, and the volume of the hexane is half of the volume of the suspension.

2. The method of claim 1, wherein the fermentation broth consists of sucrose (25 g.Math.L.sup.1), yeast extraction (5 g.Math.L.sup.1), tryptone (5 g.Math.L.sup.1), K.sub.2HPO.sub.4.3H.sub.2O (2.62 g.Math.L.sup.1), KH.sub.2PO.sub.4 (1 g.Math.L.sup.1) and MgSO.sub.4 (0.5 g.Math.L.sup.1), with an initial pH value of 7.5.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1: Effect of different concentrations of sodium selenite on the growth of E. cloacae Z0206;

(2) FIG. 2: Changes of sodium selenite residue in E. cloacae Z0206 fermentation broth at different concentrations of sodium selenite;

(3) FIG. 3: Average consumption rate of sodium selenite by E. cloacae Z0206 at different concentrations of sodium selenite;

(4) FIG. 4: Environmental scanning electronic microscope (ESEM) analysis and energy dispersive x-ray spectrum (EDX) analysis of E. cloacae Z0206 cells and biogenic elemental selenium nanostructures. (A) ESEM images; (B) Merge of the element distribution maps of carbon and selenium; (C) Element distribution map of carbon; (D) Element distribution map of selenium; (E) EDX analysis.

(5) FIG. 5: Transmission electronic microscope (TEM) analysis and EDX analysis of E. cloacae Z0206 cell and biogenic elemental selenium nanostructures. (A) TEM images; (B) EDX analysis of particle 1; (C) EDX analysis of particle 2; (D) EDX analysis of particle 3; (E) EDX analysis of particle 4.

(6) FIG. 6: TEM images of separated biogenic elemental selenium nanostructures.

(7) FIG. 7: Size analysis of separated biogenic elemental selenium nanostructures.

DETAILED DESCRIPTION OF THE INVENTION

Embodiment 1: Effect of Different Concentrations of Sodium Selenite on E. Cloacae Z0206 Growth and Selenite Reduction Rate

(8) 1. Broth Preparation

(9) LB broth: 10 g NaCl, 10 g tryptone and 5 g yeast extraction were dissolved in 1 L double distilled water, sterilized at 100 kPa, 121 C. for 20 min.

(10) LB agar plate: 10 g NaCl, 10 g tryptone, 5 g yeast extraction and 15 g agar were dissolved in 1 L double distilled water, sterilized at 100 kPa, 121 C. for 20 min.

(11) Fermentation broth: 25 g sucrose, 5 g yeast extraction, 5 g tryptone, 2.62 g K.sub.2HPO.sub.4.Math.3H.sub.2O, 1 g KH.sub.2PO.sub.4 and 0.5 g MgSO.sub.4 were dissolved in 1 L double distilled water, adjusted the initial pH value to 7.5, sterilized at 67 kPa, 115 C. for 30 min.

(12) 2. Bacteria Activation

(13) Bacterial stock from 80 C. was thawed, a loop of bacteria was taken and streaked on LB agar plate, cultivated at 32 C. for 24 h.

(14) A single colony was picked and inoculated into LB broth, cultivated at 32 C., 250 rpm for 18 h.

(15) 3. Inoculation and Fermentation

(16) Cell density was adjusted to OD.sub.600=0.5 with PBS, 1% of the bacteria cells were inoculated to fermentation broth containing 0 mM, 0.5 mM, 1 mM, 5 mM, 10 mM and 15 mM sodium selenite, respectively. Each concentration gradient was repeated for three times. Cells were fermented at 32 C., 250 rpm, and the fermentation broth was collected at 4 h, 8 h, 12 h, 16 h, 20 h, 24 h, 36 h, 48 h, 72 h and 96 h after inoculation for detecting cell protein content in order to characterize bacterial cell density; fermentation broth was also collected at 0 h, 12 h, 24 h, 36 h, 48 h, 72 h, 96 h, 120 h, 144 h and 168 h after inoculation for detecting sodium selenite residue.

(17) 4. Results

(18) As shown in FIG. 1, growth of control group E. cloacae Z0206 reached stationary phase at 12 h, while addition of sodium selenite significantly decreased the growth rate of E. cloacae Z0206, and the inhibition increased with the increase of sodium selenite concentration.

(19) FIGS. 2-3 show the sodium selenite reduction rates of E. cloacae Z0206 at different concentrations of sodium selenite. E. cloacae Z0206 started to consume sodium selenite at the beginning of cultivation. Sodium selenite of groups of 0.5 mM, 1 mM, 5 mM and 10 mM was completely consumed at 48 h, 48 h, 72 h and 144 h after inoculation, respectively. Sodium selenite reduction rate of the 15 mM group was only 91.35%1.40% at the end of point of monitoring (168 h).

Embodiment 2: Synthesis of Biogenic Elemental Selenium Nanostructure Using E. Cloacae Z0206 and Sodium Selenite

(20) Activated E. cloacae Z0206 cell density was adjusted to OD.sub.600=0.5 with PBS, 1% of the bacteria cells were inoculated to the fermentation broth, sodium selenite solution was added to a final concentration of 10 mM, cultivated at 32 C., 250 rpm for 144 h.

Embodiment 3: Electronic Microscope Analysis and Energy-Dispersive X-Ray Spectroscopy Analysis of Bacteria Cells and Biogenic Elemental Selenium Nanostructures

(21) 1 mL fermentation broth was collected according to the steps of Embodiment 2. After centrifugation, the sediment was washed three times with PBS and fixed with 2.5% glutaraldehyde solution for 12 h. The sediment was then washed again three times with PBS, followed by 1% osmic acid fixation, ethanol gradient dehydration, isoamyl acetate treatment, critical point drying and gold plating. Samples were analysed with environmental scanning electron microscope (ESEM) and energy-dispersive X-ray spectroscopy (EDX) analysis.

(22) As shown in FIG. 4, E. cloacae Z0206 reduced sodium selenite to regular spherical nanoparticles (FIG. 4A, indicated by arrow). These particles were monodisperse with sizes range between 100 nm to 200 nm. The extracellular nanoparticles were identified as elemental nano-selenium by EDX analysis, and these particles may be capped with a layer of carbon-containing organic matter.

(23) 1 mL fermentation broth was collected according to the steps of Embodiment 2. After centrifugation, the sediment was washed three times with PBS and fixed with 2.5% glutaraldehyde solution for 12 h. The sediment was then washed again three times with PBS, followed by agarose pre-embedding. The samples were treated with 1% osmic acid, ethanol gradient and embedding agent, followed by heating at 70 C., slicing and dying. The samples were analyzed with transmission electron microscopy (TEM) and EDX.

(24) As shown in FIG. 5, TEM analysis confirmed that E. cloacae Z0206 reduced sodium selenite to extracellularly located spherical nanoparticles, with sizes ranging between 100 nm to 200 nm. EDX analysis confirmed that these particles were elemental nano-selenium.

Embodiment 4: Biogenic Elemental Selenium Nanostructure Separation, Purification and Characterization

(25) 1. Fermentation broth according to Embodiment 2 was collected, centrifuged at 5,000g for 15 min, the sediment was discarded.

(26) 2. The supernatant was centrifuged at 4 C., 25,000g for 15 min, the supernatant was discarded and the sediment was collected.

(27) 3. The sediment was re-suspended with double distilled water, ultrasonicated at 25 W, 5 s on/5 s off for 15 min.

(28) 4. Hexane (half volume of above mentioned suspension) was added, vortexed and mixed, and let stand to stratification. The biogenic elemental selenium nanoparticles were present in the lower aqueous phase and the lower aqueous phase was collected, which was a biogenic elemental selenium nanoparticle suspension.

(29) 5. A drop of the biogenic elemental selenium nanoparticle suspension was added to a copper net, dried with paper filter, and analysed with TEM;

(30) 6. A drop of the biogenic elemental selenium nanoparticle suspension was analysed with nano-sizer to measure particle size.

(31) As shown in FIG. 6, TEM analysis showed that the biogenic elemental selenium nanoparticles were monodisperse, regular spheres, with sizes range between 100 nm to 200 nm. Particle size analysis (FIG. 7) showed that the biogenic elemental selenium nanoparticles ranged between 80 nm to 250 nm, with the average size of 144.101.14 nm.

Embodiment 5: Biogenic Elemental Selenium Nanostructure-Polysaccharides Complex Separation

(32) 1. The fermentation broth according to Embodiment 2 was collected by centrifuging at 5,000g for 15 min. The supernatant was collected.

(33) 2. Pre-cooled ethanol (3-fold volumes of the supernatant) was added to the supernatant, centrifuged at 5,000g for 15 min. The obtained sediment was the biogenic elemental selenium nanostructure-polysaccharides complex.

Embodiment 6: Application of Biogenic Elemental Selenium Nanostructure in Pig

(34) 1. Experiment Design

(35) Ninety 28-day-old weaned pigs were randomly divided into three groups, with three replicates per group, and ten pigs per replicate. The control group was fed with basic diet, the experimental group 1 was fed with basic diet supplied with 0.3 mg/kg Na.sub.2SeO.sub.3, and the experimental group 2 was fed with basic diet supplied with 0.14 mg/kg biogenic elemental selenium nanostructure. Diet composition and nutrient levels were shown in Table 1.

(36) TABLE-US-00001 TABLE 1 Basic diet and nutrient levels Composition (%) Nutrient levels Corn 59.3 Digestible energy (MJ/kg) 14.43 Dehulled soybean meal 8.0 Crude protein (%) 19.50 Extruded soybean 6.0 Ca (%) 0.79 Fermented soybean meal 7.0 Total P (%) 0.60 Whey powder 6.0 Lys (%) 1.50 Plasma protein 2.5 Thr (%) 0.98 Fish meal 3.0 Met (%) 0.52 Soybean oil 2.5 Trp (%) 0.18 monocalcium phosphate 0.9 Se (%) 0.10 Stone powder 0.8 Premix 4.0

(37) 2. Feeding and Management

(38) During the experimental process, pigs were kept in pigpen with slatted floor, automatic feeder and duckbill type drinker. Anthelmintic work and vaccination were performed according to the farm management.

(39) Growth Measurement

(40) Pig body weight was measured at 28-day-old and 67-day-old, respectively. Food consumption data was collected. Average daily feed intake, average daily weight gain and feed/gain ratio was calculated.

(41) Sample Collection

(42) After 12 h fasting, pig blood were collected and allowed to coagulation. The blood was centrifuged at 4 C., 3,000g for 15 min. Serum was collected and stored at 80 C.

(43) Serum Antioxidative and Immune Function Measurement

(44) Serum total antioxidative ability, glutathione peroxidase (GPx) activity, superoxide dismutase (SOD) activity, and malondialdehyde (MDA) concentration were detected using relevant kits according to the manufacturer's instruction.

(45) Serum IgG and IgM were measured using turbidimetric inhibition immuno assay.

(46) Serum inflammatory cytokine tumor necrosis factor alpha (TNF-), interleukin-2 (IL-2) and interleukin-6 (IL-6) were determined using enzme linked immunosorbent assay (ELISA) kit according to manufacturer's instruction.

(47) Statistics

(48) One-way analysis of variance (ANOVA) followed by a lease significant difference (LSD) multiple comparison test was used to determine the statistical significance for multiple comparisons, P<0.05 was considered statistically significant. All statistical tests were carried out using SPSS 22 software. All data are presented as the meanSD.

(49) Results

(50) (1) Effect of Biogenic Elemental Selenium Nanostructure on Pig Growth

(51) TABLE-US-00002 TABLE 2 Effect of biogenic elemental selenium nanostructure on pig growth Experimental Experimental Item Control group 1 group 2 Initial .sup.8.08 0.06 .sup.8.12 0.10 .sup.8.13 0.10 weight (kg) Final 23.75 0.49.sup.a 24.17 0.76.sup.a 25.72 0.83.sup.b weight (kg) Average daily 668.36 18.37 654.17 37.64 679.23 49.77.sup. feed intake (g) Average daily 401.71 11.56.sup.a 411.54 20.63.sup.a 451.03 23.97.sup.b gain (g) Feed/gain ratio 1.67 0.03.sup.a 1.59 0.01.sup.b 1.50 0.03.sup.c

(52) As shown in Table 2, even though there was no significant difference in average daily feed intake, pigs fed with biogenic elemental selenium nanostructure (experimental group 2) had significant increase of the average daily gain, and decreased feed/gain ratio. The effect of promoting growth by biogenic elemental selenium nanostructure was better than by sodium selenite (experimental group 1).

(53) (2) Effect of BNS on Pig Antioxidative Function

(54) TABLE-US-00003 TABLE 3 Effect of biogenic elemental selenium nanostructure on pig antioxidative function Experiment Experiment Item Control group 1 group 2 T-AOC (U/mL) 2.26 0.11.sup.a 2.51 0.16.sup.a 2.93 0.14.sup.b GPx (U/mL) 219.00 11.72.sup.a 238.56 13.07.sup.a 275.05 15.54.sup.b SOD (U/mL) 138.68 4.54.sup.a 147.94 5.89.sup.a 164.48 6.00.sup.b MDA 3.53 0.14.sup.a 3.31 0.10.sup.a 2.73 0.10.sup.b (nmol/mL)

(55) As shown in Table 3, compared with control group and experimental group 1, biogenic elemental selenium nanostructure significantly increased the activity of T-AOC, GPx and SOD, and decreased MDA concentration in experimental group 2. No significant difference of the parameters was shown comparing experimental group 1 with the control group.

(56) (3) Effect of Biogenic Elemental Selenium Nanostructure on Pig Immune Cytokines Expression

(57) TABLE-US-00004 TABLE 4 Effect of BNS on pig immune cytokines expression Experimental Experimental Item Control group 1 group 2 IgG (g/L) 2.39 0.09.sup.a 2.66 0.23.sup.ab 3.68 0.35.sup.c IgM (g/L) 0.66 0.07.sup.a .sup.0.71 0.07.sup.a 1.03 0.12.sup.b TNF- (ng/L) 33.66 5.17.sup.a 41.86 4.50.sup.ab 56.01 4.20.sup.c IL-2 (ng/L) 88.24 7.98.sup.a 108.19 10.26.sup.ab 131.38 11.80.sup.b IL-6 (ng/L) 479.44 26.84.sup.a 571.10 38.62.sup.ab 707.25 52.95.sup.c

(58) As shown in Table 4, comparing with the control group, Na.sub.2SeO.sub.3 and biogenic elemental selenium nanostructure significantly elevated serum levels of IgG, IgM, TNF-, IL-2 and IL-6. The elevated effects on all the serum levels of the biogenic elemental selenium nanostructure group reached to significant levels.

(59) Conclusions

(60) Dietary supplementation with biogenic elemental selenium nanostructure could significantly promote pig growth, decrease feed/gain ratio; and increase the levels of antioxidative activity and immune cytokines. All of the effects were more effective than those of sodium selenite.