CN106119144A - A kind of Pericarppium arachidis hypogaeae hydrolysate that converts prepares method and the bacterial strain of microbial flocculant - Google Patents

A kind of Pericarppium arachidis hypogaeae hydrolysate that converts prepares method and the bacterial strain of microbial flocculant Download PDF

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CN106119144A
CN106119144A CN201610220636.6A CN201610220636A CN106119144A CN 106119144 A CN106119144 A CN 106119144A CN 201610220636 A CN201610220636 A CN 201610220636A CN 106119144 A CN106119144 A CN 106119144A
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hydrolysate
arachidis hypogaeae
pericarppium arachidis
microbial flocculant
flocculant
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CN106119144B (en
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刘伟杰
郝艳
蒋继宏
刘聪
董振
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Jiangsu Normal University
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/38Pseudomonas
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • C12N1/205Bacterial isolates
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P1/00Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
    • C12P1/04Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes by using bacteria

Abstract

The present invention relates to a kind of Pericarppium arachidis hypogaeae hydrolysate that converts and prepare method and the bacterial strain of microbial flocculant, belong to microbial preparation field.Preparation technology is as follows: by strainPseudomonas sp.BWL918 is inoculated in seed liquor culture medium, and preparation seed liquor cultivated by 28 DEG C of shaking tables;Seed liquor being transferred in the fermentation medium with Pericarppium arachidis hypogaeae hydrolysate as carbon source in 1% ratio, 28 DEG C, 48 h cultivated by 180 rpm shaking tables;By fermentation liquid at 4 DEG C, after 10000 rpm are centrifuged 10 min, collect supernatant and be liquid microbe flocculant;Adding the dehydrated alcohol of 2 times of volume pre-coolings in liquid fermentation liquid, centrifugal collecting precipitate lyophilization obtain sterling microbial flocculant.The present invention can utilize Pericarppium arachidis hypogaeae hydrolysate to produce microbial flocculant as the carbon source of fermentation medium, can reduce the production cost of microbial flocculant, adapt to large-scale production and industrial applications.

Description

A kind of Pericarppium arachidis hypogaeae hydrolysate that converts prepares method and the bacterial strain of microbial flocculant
Technical field
The present invention relates to a kind of Pericarppium arachidis hypogaeae hydrolysate that converts and prepare method and the bacterial strain of microbial flocculant, be specifically related to profit WithPseudomonas Sp.BWL918 converts the method for Pericarppium arachidis hypogaeae hydrolysate fermenting and producing microbial flocculant.
Background technology
China is large agricultural country, can produce the agricultural wastes of about 700,000,000 tons, such as corn stalk in annual agricultural production process Stalk, Pericarppium arachidis hypogaeae, soil dynamic test and rice husk etc., people are usually taken burn processing, but this not only wastes resource, and pollute ring Border.Containing abundant cellulose substances in these residues, saccharide can be changed into, thus produce other high value added products, The most effectively these cellulose family agricultural wastes are converted into value product and there is important economic implications.
Flocculant is that a class can assemble the material of particle in sedimentation solution, is broadly divided into inorganic flocculating agent (such as sulfur Acid aluminum, bodied ferric sulfate etc.), organic polymer coargulator (such as polymine, polyacrylamide etc.) and natural polymer wad a quilt with cotton Solidifying agent (such as modified starch, chitosan, sodium alginate, chitin and microbial flocculant etc.).Inorganic flocculating agent is in China market On account for important share, have the demand of hundreds of thousands ton every year, mainly with iron salt, aluminium salt is representative.Iron salt has corrosivity, easily Forming residual, the water after process, with color, causes secondary pollution;Find on hygiology that aluminium salt accumulation in human body is with current Senile dementia has direct relation.Organic polymer coargulator extensively should due to its good flocculating effect and low cost In actual production, with polyacrylamide as representative, but its difficult degradation, monomeric acrylamide is a kind of strong carcinogen, and There is strong neurotoxicity, residue in the acrylamide monomer in environment and easily cause secondary pollution, the environmentally safe and mankind Health causes and has a strong impact on.Although the natural macromolecule flocculating agents such as chitosan, sodium alginate, chitin are nontoxic, energy safe disposal, But its flocculation activity is more weak, relatively costly, limits it and extensively apply;Microbial flocculant is novel third generation flocculant, It is the metabolite produced by microorganism, such as glycoprotein, mucopolysaccharide, protein, cellulose etc., has nontoxic, safety Height, the feature such as biological degradable and non-secondary pollution, therefore microbial flocculant can be widely used in sewage disposal, especially Being the advantage in the technique such as post processing of food and fermentation industry with uniqueness, its research is increasingly subject to pay attention to.
The bacterium for producing flocculant of microbe strain reported for work at present has tens kinds, such as Bacillus licheniformis X14 The microbial flocculant produced mainly is made up of neutral sugar and protein, and its Optimal compositions of fermentation medium is glucose 20 g/L, ferment Female powder 0.5g/L, carbamide 0.5g/L;Bacillus firmusS-14 can produce a kind of polysaccharide biological flocculant, its Optimal compositions of fermentation medium is glucose 10 g/L, yeast powder 0.5g/L;BacillusSp. the biological flocculant that F19 is produced Mainly being made up of neutral sugar, alduronic acid, amino sugar and protein etc., its Optimal compositions of fermentation medium is sucrose 20 g/L, yeast powder 2.5 g/L.These strain used mediums are many using expensive saccharide as key component, cause microbial flocculant production cost Height, limits the industrial applications of microbial flocculant.
In order to reduce the production cost of microbial flocculant, Guo etc. utilizes corn straw hydrolysate as bacterial strainRhodococcuserythropolisFermenting carbon source produce microbial flocculant (Bioresource Technology. 2015;177:393-397);Wang etc. utilize rice husk hydrolysate as bacterial strainOchrobactiumciceriThe fermenting carbon source of W2 produces microbial flocculant (Bioresource Technology, 2013,145:259-263);Chin-Hang Shu et al. also utilizes rice husk hydrolysate conductSchizophyllum communeCulture medium produce microbial flocculant (Journal of the Taiwan Institute of Chemical Engineers, 2011, 42(3): 387-393).But have no at present and utilize Pericarppium arachidis hypogaeae water Solve thing and produce the research of microbial flocculant as fermentation medium.The annual peanut yield of China about more than 1,500 ten thousand tons, occupies the world First, the annual Pericarppium arachidis hypogaeae garbage producing about 5,000,000 tons, these Pericarppium arachidis hypogaeae garbages are commonly used as fuel, cause resource Waste and environmental pollution.Containing materials such as abundant cellulose, starch in Pericarppium arachidis hypogaeae, have and develop other high value added products Potentiality.Bacterial strain uses therefor of the present invention is that we separate the pseudomonas of acquisitionPseudomonas Sp.BWL918, this bacterial strain energy Utilize Pericarppium arachidis hypogaeae hydrolysate fermenting and producing microbial flocculant, the production cost of microbial flocculant can be effectively reduced, become Waste be changed into values, it is achieved the recycling of Pericarppium arachidis hypogaeae.
Summary of the invention
The invention provides onePseudomonas Sp.BWL918 bacterial strain and convert Semen arachidis hypogaeae in neutral conditions Shell hydrolysate produces the method for high-activity microorganism flocculant.This bacterial strain has fast growth, and fermentation period is short, and flocculant produces Amount advantages of higher, it is possible to be effectively reduced the production cost of microbial flocculant.
The present invention includes herein below: a kind of Pericarppium arachidis hypogaeae hydrolysate that converts prepares the bacterial strain of microbial flocculantPseudomonas Sp.BWL918, is preserved in China General Microbiological culture presevation administrative center, and preservation address is Beijing North Star West Road, Chaoyang District, city 1 institute 3, culture presevation number is CGMCC 11994, preservation date 2016.01.12.
One utilizes bacterial strainPseudomonas Sp.BWL918 converts Pericarppium arachidis hypogaeae hydrolysate and prepares microbial flocculant Method, the processing step of the method is as follows:
Step 1, Pericarppium arachidis hypogaeae is pulverized, and sieve with 60 mesh mesh screens, by the concentration of 100g/L, peanut hull meal is added 1.7%(W/W) H2SO4In solution, hydrolyze 120 min in 121 DEG C, after cooling, centrifugal 10 min, collect supernatant, with Ca (OH)2Regulation pH To 7.0, recentrifuge 10 min, collects supernatant and obtains the Pericarppium arachidis hypogaeae hydrolysate carbon source for subsequent fermentation culture medium;
Step 2, being inoculated into by strain in seed liquor culture medium, 12 h cultivated by 28 DEG C of shaking tables, prepare seed liquor;
Step 3, seed liquor being transferred to using Pericarppium arachidis hypogaeae hydrolysate as the fermentation medium of carbon source in the ratio of 1%, shaking table is trained Support 48 h;
Step 4, by fermentation medium at 4 DEG C, centrifugal 10 min, collect supernatant and be liquid microbe flocculant;
Step 5, the dehydrated alcohol of 2 times of volume pre-coolings of addition, centrifugal collecting precipitate, and freezing in liquid microbe flocculant It is dried to obtain microbial flocculant product.
Further, the seed liquor culture medium described in step 2 is glucose 1 g/L, soluble starch 1 g/L, yeast Powder 1 g/L, tryptone 1 g/L, acid hydrolyzed casein 1 g/L, Magnesium sulfate heptahydrate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L, The cultivation temperature of seed liquor is 28 DEG C.
Further, the shaking table condition of culture in step 3 is 28 DEG C, and 48 h cultivated by 180 rpm shaking tables.
Further, the fermentation medium described in step 3 is Pericarppium arachidis hypogaeae hydrolysate 300mL/L, yeast powder 3 g/L, seven Water magnesium sulfate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L, the initial pH of fermentation liquid are 7.0.
Further, the centrifugal rotational speed of step 1 and step 4 is 10000 rpm.
Further, in described step 5, in the liquid microbe flocculant that step 4 obtains, add 2 times of volume pre-coolings Dehydrated alcohol, 10000 rpm be centrifuged 10 min collect precipitation, 70% washing with alcohol precipitation after, lyophilization obtain microorganism wadding Solidifying agent sterling.
The present invention compared with prior art, has the advantage that present invention firstly provides and utilizes Pericarppium arachidis hypogaeae hydrolysate to produce Microbial flocculant, it is possible to achieve the recycling to Pericarppium arachidis hypogaeae, reduces environmental pollution.Bacterial strain involved in the present inventionPseudomonas Sp.BWL918 fast growth, fermentation period is short, and microbial flocculation yield is high, well should have Use prospect.
Detailed description of the invention
A kind of Pericarppium arachidis hypogaeae hydrolysate that converts prepares the bacterial strain of microbial flocculantPseudomonas Sp.BWL918, Being preserved in China General Microbiological culture presevation administrative center, culture presevation number is CGMCC 11994.
A kind of convert Pericarppium arachidis hypogaeae hydrolysate to prepare the processing step of microbial flocculant as follows:
Step 1, by strainPseudomonas Sp., during BWL918 is inoculated into seed liquor culture medium, 28 DEG C of shaking flasks are overnight trained Support preparation seed liquor;
Step 2, seed liquor is transferred in the fermentation medium with Pericarppium arachidis hypogaeae hydrolysate as carbon source in 1% ratio, 28 DEG C, 180 48 h cultivated by rpm shaking table;
Step 3, by fermentation medium at 4 DEG C, 10000 rpm are centrifuged 10 min, remove precipitation, and supernatant is liquid bio wadding Solidifying agent;
Step 4, in liquid fermentation liquid add 2 times of volume pre-coolings dehydrated alcohol, centrifugal collecting precipitate lyophilization obtain To sterling biological flocculant.
In described step 1, strain used is pseudomonasPseudomonas Sp.BWL918, patent culture presevation Number it is CGMCC 11994, Pericarppium arachidis hypogaeae hydrolysate can be utilized to produce microbial flocculant;
In described step 1, seed liquor medium component is as follows: glucose 1 g/L, soluble starch 1 g/L, yeast powder 1 g/ L, tryptone 1 g/L, acid hydrolyzed casein 1 g/L, Magnesium sulfate heptahydrate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L;
In described step 2, the preparation process of Pericarppium arachidis hypogaeae hydrolysate is as follows: pulverized by Pericarppium arachidis hypogaeae pulverizer, with 60 mesh mesh screens Sieve, by the concentration of 100g/L, peanut hull meal added 1.7%(W/W) H2SO4In solution, 121 DEG C of hydrolysis 120 min, cooling After, centrifugal collection supernatant, with Ca (OH)2Regulation pH to 7, recentrifuge is collected supernatant and is obtained Pericarppium arachidis hypogaeae hydrolysate;
In described step 2, the composition of fermentation medium is as follows: Pericarppium arachidis hypogaeae hydrolysate 300 mL/L, yeast powder are nitrogen source 3 g/ L, Magnesium sulfate heptahydrate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L.
Specific embodiment 1: microbial flocculant preparation method, specifically comprises the following steps that
1, strain separating and qualification: utilize gradient dilution method separation screening function stem, described screening and culturing based component is: Portugal Grape sugar 0.5 g/L, soluble starch 0.5 g/L, yeast powder 0.5 g/L, tryptone 0.5 g/L, acid hydrolyzed casein 0.5 G/L, Magnesium sulfate heptahydrate 0.05g/L, dipotassium hydrogen phosphate 0.3g/L.After strain separating obtains, obtained by four zoning collimation method method of purification To purebred bacterial strain, through 16S rRNA sequence analysis determine strain used by the present invention be pseudomonas (Pseudomonas And it is named sp.),Pseudomonas Sp. BWL918, patent culture presevation number is CGMCC 11994
2, prepared by seed liquor: by pseudomonasPseudomonas Sp.BWL918 is seeded in seed liquor culture medium, Seed liquor nutrient media components is as follows: glucose 1 g/L, soluble starch 1 g/L, yeast powder 1 g/L, tryptone 1 g/L, acid Caseinhydrolysate 1 g/L, Magnesium sulfate heptahydrate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L.Then 28 DEG C, 180 rpm incubator overnight Cultivate.
3, microbial flocculant is prepared in fermentation: seed liquor step 2 obtained is seeded in fermentation medium in 1% ratio, Fermentation medium component is as follows: peanut hull meal hydrolysate 300mL/L;Yeast powder 3 g/L, Magnesium sulfate heptahydrate 0.1 g/L, phosphoric acid Hydrogen dipotassium 0.6 g/L;Then 28 DEG C, 180rpm shaker fermentation cultivates 48h.
4, microbial flocculant extracts: fermentation liquid step 3 obtained is centrifugal 10 min under the conditions of 10000 rpm, receive Collection supernatant;Adding the dehydrated alcohol of 2 times of volume pre-coolings in supernatant, 10000 rpm are centrifuged 10 min and collect precipitation, use After 70% washing with alcohol precipitation, lyophilization obtains microbial flocculant sterling.
5, flocculation activity measures: add 100 μ L fermentation liquids in 60 mL5 g/L Kaolin suspensions;Quickly stirring 2 Min, is then slowly stirred 1 min, standing sedimentation 1 min, takes supernatant 722 type spectrophotometric determination OD550Value, to add Enter 100 μ L distilled water as comparison, represent flocculation activity by calculating flocculating rate.Flocculating rate=(A-B)/A × 100%, A represents The OD of supernatant when adding distilled water550Value, B represents with the OD of supernatant during fermentation liquid550Value.The microbial flocculant pair obtained Aqueous suspension ofkaolin has obvious flocculating effect.

Claims (7)

1. one kind converts Pericarppium arachidis hypogaeae hydrolysate and prepares the bacterial strain of microbial flocculantPseudomonas Sp.BWL918, preservation In China General Microbiological culture presevation administrative center, culture presevation number is CGMCC 11994.
2. the method that conversion Pericarppium arachidis hypogaeae hydrolysate as claimed in claim 1 prepares microbial flocculant, the work of the method Skill step is as follows:
Step 1, Pericarppium arachidis hypogaeae is pulverized, and sieve with 60 mesh mesh screens, by the concentration of 100g/L, peanut hull meal is added 1.7%(W/W) H2SO4In solution, hydrolyze 120 min in 121 DEG C, after cooling, centrifugal 10 min, collect supernatant, with Ca (OH)2Regulation pH To 7.0, recentrifuge 10 min, collects supernatant and obtains the Pericarppium arachidis hypogaeae hydrolysate carbon source for subsequent fermentation culture medium;
Step 2, being inoculated into by strain in seed liquor culture medium, 28 DEG C of shaking tables are cultivated 12 h and are prepared seed liquor;
Step 3, seed liquor being transferred to using Pericarppium arachidis hypogaeae hydrolysate as the fermentation medium of carbon source in the ratio of 1%, shaking table is trained Support 48 h;
Step 4, by fermentation medium at 4 DEG C, centrifugal 10 min, collect supernatant and be liquid microbe flocculant;
Step 5, the dehydrated alcohol of 2 times of volume pre-coolings of addition, centrifugal collecting precipitate, and freezing in liquid microbe flocculant It is dried to obtain microbial flocculant product.
The most according to claim 1 a kind of converting the method that Pericarppium arachidis hypogaeae hydrolysate prepares microbial flocculant, its feature exists In, the seed liquor culture medium described in step 2 is glucose 1 g/L, soluble starch 1 g/L, yeast powder 1 g/L, Trypsin Peptone 1 g/L, acid hydrolyzed casein 1 g/L, Magnesium sulfate heptahydrate 0.1 g/L, dipotassium hydrogen phosphate 0.6 g/L, the cultivation temperature of seed liquor Degree is 28 DEG C.
The most according to claim 1 a kind of converting the method that Pericarppium arachidis hypogaeae hydrolysate prepares microbial flocculant, its feature exists In, the shaking table condition of culture in step 3 is 28 DEG C, and 48 h cultivated by 180 rpm shaking tables.
The most according to claim 1 a kind of converting the method that Pericarppium arachidis hypogaeae hydrolysate prepares microbial flocculant, its feature exists In, the fermentation medium described in step 3 is Pericarppium arachidis hypogaeae hydrolysate 300mL/L, yeast powder 3 g/L, Magnesium sulfate heptahydrate 0.1 g/ L, dipotassium hydrogen phosphate 0.6 g/L, the initial pH of fermentation liquid are 7.0.
The most according to claim 1 a kind of converting the method that Pericarppium arachidis hypogaeae hydrolysate prepares microbial flocculant, its feature exists In, the centrifugal rotational speed of step 1 and step 4 is 10000 rpm.
The most according to claim 1 a kind of converting the method that Pericarppium arachidis hypogaeae hydrolysate prepares microbial flocculant, its feature exists In, in described step 5, in the liquid microbe flocculant that step 4 obtains, add the dehydrated alcohol of 2 times of volume pre-coolings, 10000 rpm are centrifuged 10 min and collect precipitation, and after 70% washing with alcohol precipitation, lyophilization obtains microbial flocculant sterling.
CN201610220636.6A 2016-04-11 2016-04-11 A kind of conversion peanut shell hydrolysate prepares the method and bacterial strain of microbial flocculant Expired - Fee Related CN106119144B (en)

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