CN113528399B

CN113528399B - Pediococcus acidilactici with hexavalent chromium ion reducing capacity and application thereof

Info

Publication number: CN113528399B
Application number: CN202110950722.3A
Authority: CN
Inventors: 郭旭生; 黄文康; 马莹; 刘芳
Original assignee: Lanzhou University
Current assignee: Lanzhou University
Priority date: 2021-08-18
Filing date: 2021-08-18
Publication date: 2023-02-10
Anticipated expiration: 2041-08-18
Also published as: CN113528399A

Abstract

The invention belongs to the field of microbial strains, and relates to pediococcus acidilactici with hexavalent chromium ion reducing capacity and application thereof, wherein the pediococcus acidilactici is pediococcus acidilactici (a)Pediococcusacidilacticii) 13-7, accession number: CGMCC No.21666. Can be used for fermentation of silage, and hexavalent chromium ions remained in the silage are reduced into trivalent chromium ions in the fermentation process. Has the advantages that: the pediococcus acidilactici has hexavalent chromium reducing capability, can reduce hexavalent chromium ions in silage, soil and the like into trivalent chromium ions, is an environment-friendly treatment mode, and reduces the toxic hazard of chromium ion accumulation to livestock and human bodies.

Description

Pediococcus acidilactici with hexavalent chromium ion reducing capability and application thereof

Technical Field

The invention belongs to the technical field of microorganism application, and relates to pediococcus acidilactici with hexavalent chromium ion reducing capacity.

Background

Under the natural environment condition, hexavalent chromium ions are accumulated in planting soil and irrigation water due to environmental pollution. Hexavalent chromium ions have strong oxidizing property and cause irreversible oxidative damage to animals after being eaten by the animals. And because hexavalent chromium is difficult to be discharged out of the body through a general biological metabolism path, the damage of the hexavalent chromium can be gradually accumulated along with the ingestion of forage grass polluted by the hexavalent chromium by animals. Can finally accumulate in human body through food chain, causing damage to human body.

The hexavalent chromium remaining in the silage such as alfalfa and the like is removed by the existing means, the operation is complicated, the cost is high, the longer treatment time influences the process of manufacturing the silage, and therefore, the finding of a suitable method for reducing the chromium pollution in the silage is of great significance.

Lactic acid bacteria are widely used as probiotics, and are widely used as additives of foods, beverages and feeds. Lactic acid bacteria have become indispensable biological products in modern human production and life as flavoring agents for food and drink, additives for fermented feed, and the like. A large number of studies have shown that some lactic acid bacteria exhibit a strong antioxidant potential. Previous people also reported that a large amount of lactic acid bacteria with antioxidant capacity are screened and selected, and the lactic acid bacteria are applied to various fields such as food, health care, animal feed additives and the like, and certain effect is achieved. However, the reduction of heavy metal chromium in the environment by the antioxidant lactic acid bacteria is rarely reported. Screening out Pediococcus acidilactici with hexavalent chromium ion reducing capability is an effective method for reducing harm of hexavalent chromium.

Disclosure of Invention

The invention aims to provide pediococcus acidilactici with hexavalent chromium ion reducing capacity and application thereof.

The technical scheme of the invention is as follows: pediococcus acidilactici with hexavalent chromium ion reducing capability, wherein the Pediococcus acidilactici is Pediococcus acidilactici (Pediococcus acidilactici)Pediococcus acidilacticii) 13-7, accession No.: CGMCC No.21666.

The pediococcus acidilactici can be used for fermentation of silage, and hexavalent chromium ions remained in the silage are reduced to trivalent chromium ions in the fermentation process, so that the risk of chromium poisoning is reduced. The pediococcus acidilactici can be prepared into a microbial inoculum, and is preserved, transported, added and used in a conventional culture and preservation mode of the pediococcus acidilactici, so that the pediococcus acidilactici is convenient to use.

Preservation information: pediococcus acidilactici: (A. Acidilactici)Pediococcus acidilacticii) 13-7, accession number: CGMCC No.21666. The preservation date is as follows: year 2021, month 19. Name of the depository: china general microbiological culture Collection center (CGMCC), the address of the collection unit: the institute of microbiology, institute of academy of sciences, china, west Lu No. 1, beijing, chaoyang, north Chen.

The invention has the beneficial effects that: the pediococcus acidilactici of the present invention has a hexavalent chromium reducing ability, and can reduce hexavalent chromium ions in silage, soil, etc. to trivalent chromium ions. For the feed, the fermentation quality of the basic silage is ensured, the residue of hexavalent chromium ions in the silage is effectively reduced, and the safety of the silage in the taking process is improved.

The trivalent chromium ion is a trace element necessary for human body, plays a special role in sugar metabolism and lipid metabolism of the human body, and has an important role in maintaining the health of the human body. The pediococcus acidilactici of the present invention can reduce highly toxic hexavalent chromium ions into trivalent chromium ions which are beneficial to human bodies, thereby achieving the purpose of reducing the toxic action on livestock and human bodies due to the accumulation of chromium ions. The treatment mode is very environment-friendly.

Drawings

FIG. 1 is a graphical representation of the hexavalent chromium reduction rate of a lactic acid bacterium having hexavalent chromium reduction capability;

FIG. 2 is a graph of the growth of strains in different media;

FIG. 3 is the result of detection of the minimum inhibitory concentration;

FIG. 4 is a graph showing the effect of bacterial supernatants at different incubation times on hexavalent chromium residues.

Detailed Description

Obtaining bacteria: screening and obtaining bacteria with hexavalent chromium reducing capability from a bacteria bank in the applicant laboratory, numbering the screened bacteria with hexavalent chromium reducing capability respectively, and freezing and storing the bacteria in the laboratory.

The culture method of the strain comprises the following steps:

lactic acid bacteria culture Medium (MRS): 10g of peptone, 10g of beef extract, 5g of yeast extract, 2g of diammonium hydrogen citrate, 20g of glucose, 1mL of Tween 80, 5g of sodium acetate, 2g of dipotassium phosphate, 0.58g of magnesium sulfate, 0.25 g of manganese sulfate, 15g of agar, 1000 mL of distilled water and pH of 6.2-6.6. The preparation method comprises the following steps: adding all the components except the agar into water, heating and dissolving, adjusting the pH value to 6.2-6.4, adding the agar, sterilizing at 121 ℃ for 15min, and pouring the mixture on a flat plate while the mixture is hot.

Phosphate Buffered Saline (PBS): 0.24g of monopotassium phosphate, 1.44g of dipotassium phosphate, 8g of sodium chloride, 0.2g of potassium chloride, 1000 mL of distilled water and pH 7.2-7.4. The preparation method comprises the following steps: mixing the above materials, dissolving in distilled water, adjusting pH, sterilizing at 121 deg.C for 15min, and cooling.

Diphenylamino urea (DPC): DPC powder 0.2g, acetone 50 mL, deionized water 50 mL. The preparation method comprises the following steps: after 0.2g of DPC powder was dissolved in acetone, deionized water was added to 100mL to prepare the DPC powder ready for use (if the DPC solution became dark, it could not be used).

20 uL of Ds45 bacterial liquid is inoculated into 1000 uL of MRS culture medium, and is statically cultured for 8-12 hours at 37 ℃. And (4) placing the cultured bacterial liquid in a high-speed centrifuge, and centrifuging at the room temperature of 12000 rpm for 10 min to obtain a fermentation supernatant. The fermentation supernatant has hexavalent chromium reducing ability.

The hexavalent chromium reducing capability of the strain is verified:

preparation of PBS buffer containing potassium dichromate: and (3) sterilizing the prepared buffer solution at 121 ℃ for 15min under high pressure, filtering the prepared potassium dichromate solution with a certain concentration through a 0.22-micron organic filter membrane, adding the filtered solution into the PBS buffer solution, and slightly shaking the bottle body to uniformly mix the solution.

Preparing a DPC color developing agent: 0.1 g of DPC reagent powder was weighed and dissolved in 25 mL of acetone. After the dissolution of the DPC powder was completed, the volume was adjusted to 50 mL with deionized water. DPC is easily decomposed by light and heat, and its powder should be stored in brown reagent bottle at 4 deg.C. The DPC solution used in the test should be ready for use, but cannot be used if the color of the DPC solution becomes dark.

The frozen strains with hexavalent chromium reduction capability in a laboratory bacterial bank are taken and activated for 3 times by using an MRS culture medium. Centrifugation was carried out at room temperature (12000 rpm,10 min). 200 uL of supernatant was taken and mixed with 800 uL of the prepared potassium dichromate PBS solution. Reacting in a constant temperature incubator at 37 ℃ for 24 hours, and detecting the residual quantity of hexavalent chromium ions by using a DPC method.

As can be seen from FIG. 1, the supernatants from the 24h fermentations of strains 13-7 and Ds45 showed considerable reducing power in both the 0.2mM and 0.4mM hexavalent chromium reduction tests. When the concentration of hexavalent chromium is 0.2mM, the reduction rate of hexavalent chromium of the supernatant with 13-7, 19-5x-Ds45 and am21 is more than 50%, and after the supernatant is cultured for 24 hours at 13-7 and Ds45, the reduction rate of 0.2mM hexavalent chromium ions by the supernatant can reach 88% to the maximum. Further, the reduction comparison of the supernatant was performed using a solution of 0.4mM hexavalent chromium, in which only 13-7 and Ds45 were more than 50% in reduction, in which the reduction of 0.4mM hexavalent chromium was 54.5% in 13-7 supernatant and the reduction of 0.4mM hexavalent chromium was 55% in Ds45 fermentation supernatant. Because the reduction of the strain is based on metabolites in the supernatant, the strain has different application prospects in practical application with most of the existing lactobacillus which is mainly used for treating hexavalent chromium pollution by taking the adsorption effect as the main part, and can also be used together with the lactobacillus with the adsorption effect to achieve better hexavalent chromium treatment effect. Therefore, these two lactic acid bacteria were selected as strains for subsequent experiments.

Characterization of strains 13-7 and Ds45

MRS liquid medium: 20g of glucose, 10g of beef extract, 5g of yeast powder, 5g of anhydrous sodium acetate, 2g of diammonium hydrogen citrate, 2g of dipotassium hydrogen phosphate, 0.58g of magnesium sulfate heptahydrate, 0.17g of manganese sulfate monohydrate and-80 mL of polysorbate. 1L of distilled water was added.

MRS solid medium: on the basis of MRS liquid culture medium, 15g of agar powder is added into every 1L of liquid culture medium, and after sterilization is carried out for 20min at 121 ℃, the liquid culture medium is slightly placed for cooling and poured into a disposable culture dish. The prepared solid culture medium is placed upside down in a super clean bench for standby.

PBS buffer: BS buffer solution: 0.24g of potassium dihydrogen phosphate, 1.44g of disodium hydrogen phosphate, 8g of sodium chloride and 0.2g of potassium chloride. The powder was dissolved with 800 mL of deionized water and adjusted to pH 7.4 with HCl and then made up to 1L.

Physiological saline: 0.85g of sodium chloride is added into each 100mL of distilled water, and the mixture is sterilized for 20min at 121 ℃.

Preparing an MRS liquid culture medium containing potassium dichromate: subpackaging common MRS liquid culture medium into blue-mouth bottles, and sterilizing at 121 deg.C for 20min. Filtering potassium dichromate solution with required concentration with 0.22 um organic phase filter membrane in a clean bench, adding into sterilized MRS liquid culture medium, shaking up gently, and storing at room temperature.

Preparing an MRS solid culture medium containing potassium dichromate: on the basis of a common MRS liquid culture medium, the MRS culture medium is firstly subpackaged into blue-mouth bottles according to 100 mL/bottle, then 1.5g of agar powder is added into each bottle, and the bottles are placed into an autoclave for sterilization at 121 ℃ for 20min. While waiting for sterilization, a gradient solution of potassium dichromate was prepared. A potassium dichromate solution up to 48mM was prepared in a volume of 100mL, and then 12 parts were sequentially diluted in a 1/2 gradient. Then filtering with 0.22 um sterile organic filter membrane in a clean room, and placing the prepared solid culture medium upside down in a clean bench for standby. After the sterilization is finished, the culture medium is slightly placed for a period of time, after the temperature of the culture medium is reduced to the temperature capable of holding the bottle body, potassium dichromate solutions with different concentrations are added into an ultra-clean workshop, and the plate is poured. At least 6 plates per flask of medium should be made.

Determination of the growth curve of the strain: taking out the strains 13-7 and Ds45 from a refrigerator at the temperature of-80 ℃, carrying out streak culture for 24-48h, observing whether the colony morphology on the plate is consistent or not after the single colony grows to the proper size and density, picking the single colony into 1mL of MRS liquid culture medium on an ultra-clean workbench, and carrying out overnight culture.

Several 10 mL centrifuge tubes were prepared and the overnight cultured strains were inoculated in 5mL of ordinary MRS medium or MRS medium containing potassium dichromate in an inoculum size of 1%. The test set was used individually at each time point of testing and the tube was discarded after testing.

Because the growth speed of the lactobacillus is higher from the early growth stage to the end of the logarithmic growth phase, the detection time points at the early stage are more densely arranged, and the detection time points at the middle and later stages are relatively loose. The inoculated 10 mL centrifuge tube should be sealed by using a sealing film or an adhesive tape, otherwise, the centrifuge tube cover may be opened or not sealed tightly due to the pressure difference generated by the gas substances generated during the growth of the lactic acid bacteria, so that air and other miscellaneous bacteria enter the tube, the growth of the test strains is influenced, and the accuracy of the test result is finally influenced.

Before each detection, the spectrophotometer is started in advance and preheated for about 30min. Each time, the liquid is poured into a cuvette with a volume of 1/3-2/3, and the absorption wavelength is detected using 600 nm. An unheated spectrophotometer may also cause variations in test results. Distilled water is used for cleaning the cuvette every time the sample is added into the cuvette, and the cuvette is rinsed by the sample to be detected in advance, otherwise the colorimetric result can be influenced by the residue of the previous sample or the residue of the distilled water.

The results of the strain growth curve test are shown in FIG. 2. After streaking activation of the strain according to the general method, the strain was cultured in a 10 mL centrifuge tube in batches to examine the growth curve of the strain. In order to test the resistance of the strain to hexavalent chromium in the culture medium solution, the growth curve of the strain in the MRS medium with hexavalent chromium is tested using an equal volume of MRS solution to which 0.4mM hexavalent chromium solution is added. Based on the characteristics that the bacteria grow slowly in the early stage, grow fast after entering the logarithmic growth phase, and the bacterial strains basically stop growing after passing the logarithmic growth phase, the detection time points with denser early stage and looser later stage are set. According to the growth curve result detected by the strain, the addition of 0.2mM potassium dichromate in the MRS culture medium does not affect the normal growth capability of the strain, but can slightly improve the growth speed of the strain in the logarithmic growth phase. When the strain grows in the MRS culture medium added with potassium dichromate, the final bacterial count of the strain reaching the logarithmic growth phase, entering the stationary phase and entering the stationary phase is the same as that of the MRS culture medium without potassium dichromate.

And (3) measuring the minimum inhibitory concentration of the hexavalent chromium reducing strain: taking out strain 13-7 and strain Ds45 from a refrigerator at-80 deg.C, streaking and activating on solid culture medium, and culturing for 24-48h. Selecting single colonies to culture in 1mL of MRS liquid culture medium for 6-12h, and stopping culture after logarithmic growth phase is reached. Centrifuging the cultured bacteria liquid in a centrifuge at 8000rpm for 2-5min, discarding supernatant in a super clean bench, and resuspending with physiological saline. The MRS medium can be used for resuspension, but the strain can grow more after being coated due to the residual ordinary MRS medium on the plate, thereby causing influence on the test result.

Detecting, diluting and adjusting the bacteria number to 10 by a spectrophotometer ⁸ CFU/mL, distilled water was used for zeroing. Dilution with saline gradient 10 in clean bench ⁵ And (4) doubling. 100 μ L of diluted inoculum was added dropwise to each plate using a pipette gun and spread evenly with a glass coating rod until no liquid was present on the surface of the solid medium. 3-4 replicates per strain were done per gradient to avoid accidental events during the growth of the strain affecting the results.

And (3) using a gradient MRS culture medium prepared in advance, wrapping the coated solid culture medium with a preservative film, taking out the wrapped solid culture medium from an ultra-clean room, putting the wrapped solid culture medium into a 37 ℃ incubator to culture for 48 hours, and counting single colonies in the culture dish, wherein the concentration of potassium dichromate which cannot grow by the lowest bacteria is taken as the minimum inhibitory concentration of the bacteria.

As can be seen from fig. 3, the resistance of the two test strains to hexavalent chromium was tested using MRS solid medium with gradient concentration of potassium dichromate, and the growth of the two test strains was significantly different only at hexavalent chromium concentrations of 1.5mM and 6 mM. The strain Ds45 still has a single colony to grow under the hexavalent chromium concentration of 12mM, and the strain Ds 13-7 has no colony to grow under the hexavalent chromium concentration of the same concentration. Therefore, the minimum inhibitory concentration of the strain Ds45 is 24mM hexavalent chromium, and the minimum inhibitory concentration of 13-7 is 12mM hexavalent chromium. In addition, when the hexavalent chromium concentration is less than 0.75mM, the control PA grows over 300 colonies on the plate, and there are cases where a plurality of colonies grow together, so that accurate counting cannot be performed. As can be seen from FIG. 3, both strains have strong resistance to hexavalent chromium, up to a concentration of 12mM potassium dichromate, i.e., 24mM hexavalent chromium. Metabolites generated by the two strains in the growth process are verified to have certain hexavalent chromium reduction capability, so that the metabolites can still be grown in a solid culture medium to a certain extent, and the damage of hexavalent chromium in the culture medium to the strains is reduced. The two strains have stronger growth activity, can be quickly propagated in a flat plate with low chromium ion concentration depending on the number of basic bacteria, and can clear surrounding hexavalent chromium and weaken the toxicity of a culture medium depending on the reduction capability of the strain to the hexavalent chromium, so that the subsequent strains can grow more normally. In MRS culture medium containing high-concentration potassium dichromate, the thalli cannot accumulate reducing substances due to the use of physiological saline washing bacteria, so that the thalli can not grow and reproduce when the concentration of hexavalent chromium exceeds the bearing capacity of the thalli.

Determination of the relationship between the strain culture time and the reduction ability of the supernatant: taking out the strain 13-7 and the strain Ds45 from a refrigerator at minus 80 ℃, streaking and activating on an MRS solid culture medium, culturing for 24-48h, picking out a single strain to be dropped into 1mL of MRS liquid culture medium, repeating the activation twice, culturing for 24h in an incubator at 37 ℃ after the activation for the last time, taking out a sample when the culture time reaches 1, 2, 3, 4, 5, 6, 8, 10, 12 and 24h, centrifuging for 2-5min at 12000 rpm by using a high-speed centrifuge, and adding 100 mu L of supernatant into 900 mu L of PBS-potassium dichromate solution prepared in advance in a super clean workbench. Placing the solution into an incubator at 37 ℃, standing for 24 hours, and detecting the hexavalent chromium residue of the reduced solution by using a DPC method.

As can be seen from FIG. 4, both strains achieved the theoretical reduction rate at the time of screening after 24h of culture. The whole trend of the residual quantity of hexavalent chromium in the hexavalent chromium solution treated by the supernatants of the two strains is gradually reduced, namely the reduction capability of the supernatants to the hexavalent chromium is gradually enhanced along with the increase of the culture time. When the culture time of the supernatant is within 3h, the residual hexavalent chromium of the Ds45 treated solution is higher, and when the culture time reaches 4h, the residual hexavalent chromium in the supernatant treated by the Ds45 and the supernatant treated by the Ds45 are not obviously different until the residual hexavalent chromium in the solution treated by 13-7 is higher than the residual hexavalent chromium in the Ds45 after 12 h. And in the culture process, the residual quantity of hexavalent chromium in the solution treated by 13-7 at the first 3h and Ds45 at the first 4h slightly increases.

The pediococcus acidilactici with the hexavalent chromium ion reducing capability of the invention can also be used for food industry and chromium pollution treatment. Has the potential of being used as a probiotic additive in feed production and food addition. The bacterium can be added into food requiring fermentation of pediococcus acidilactici, such as yogurt and sauerkraut. The pediococcus acidilactici with the hexavalent chromium ion reducing capability can be prepared into a microbial inoculum which is scattered in chromium-polluted soil or water body to reduce the highly toxic hexavalent chromium ions into trivalent chromium ions, so that the harm of chromium pollution is reduced.

Claims

1. The pediococcus acidilactici with the hexavalent chromium ion reducing capability is characterized in that: the bacterium is Pediococcus acidilactici (Pediococcus acidilacticii) 13-7, accession number: CGMCC No.21666.

2. A microbial agent comprising Pediococcus acidilactici having hexavalent chromium ion reducing ability according to claim 1, wherein the Pediococcus acidilactici is stored, transported, added and used by a conventional culture and storage method of Pediococcus acidilactici.