CN102115723B - Bacillus amyloliquefaciens LC02 and application thereof - Google Patents
Bacillus amyloliquefaciens LC02 and application thereof Download PDFInfo
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- CN102115723B CN102115723B CN 201010569921 CN201010569921A CN102115723B CN 102115723 B CN102115723 B CN 102115723B CN 201010569921 CN201010569921 CN 201010569921 CN 201010569921 A CN201010569921 A CN 201010569921A CN 102115723 B CN102115723 B CN 102115723B
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Abstract
The invention discloses a preparation method of bacillus amyloliquefaciens LC02 (CGMCC No.4258) spore laccase, the catalysis capability and the application in the decoloring the dye. The invention further relates to a nucleotide sequence which codes the spore laccase. The bacillus amyloliquefaciens LC02 is fermented on a solid state spore generating culture medium at 37 DEG C for 5 days, and the spore is washed by the deionized water to obtain the spore suspension liquid with the laccase activity by a series of measures such as the lysozyme. The spore laccase is better in catalytic activity under the alkaline and high-temperature conditions, is better in a decoloring effect to the synthetic dyes with different structures under the action of a medium, and is used for treating the industrial dye waste water.
Description
Technical field
The present invention relates to a kind of bacterial laccase, be specifically related to preparation method and the catalytic property of the gemma laccase of a bacillus amyloliquefaciens LC02, and the nucleic acid fragment of this gemma laccase of encoding.In addition, the invention still further relates to the method that this gemma laccase makes synthetic dyestuff decolourings, belong to the using microbe field.
Background technology
Laccase (EC 1.10.3.2) is a kind of polyphenoloxidase of cupric, and it can utilize the aromatic compound of the Copper ioncatalyst oxidation various structures in active centre, simultaneously molecular oxygen is reduced into water.Because the substrate scope of Laccase Catalyzed is very extensive, so the laccase enzyme has been widely used in the fields such as biological restoration of paper industry, textile industry, foodstuffs industry and soil.
The Laccase Catalyzed oxidation substrates generally comprises two kinds of modes of action, the first be substrate molecule directly and bunch reaction of laccase copper be oxidized to corresponding excited state molecule.Yet some substrate can not be by the laccase direct oxidation, and reason is that their molecules can not penetrate into the reactive site of enzyme too greatly, perhaps can not be by the laccase direct oxidation because its redox potential is higher.The second way of laccase oxidation substrates is to be medium by some micromolecular amboceptor materials, laccase first is oxidized to excited state with the small molecules amboceptor, then the amboceptor of these excited state again with substrate reactions macromolecular or that redox potential is higher, this mode is also referred to as laccase-mediator system (LMS).The application of laccase-mediator system helps further to enlarge the substrate scope of laccase, improves the industrial applicability of laccase.
At occurring in nature, laccase is distributed widely in plant, fungus and bacterium, and particularly fungi, be the main producer of present laccase.Although at present the theoretical investigation of bacterial laccase is goed deep into not as fungal laccase, bacterium has the advantages that growth is fast, be easy to cultivate, bacterial laccase has better stability under alkaline environment and high temperature than the fungi laccase.Because the general temperature such as industrial paper waste is higher, alkalescence is stronger, and fungal laccase is subject to the restriction of poor stability in actual applications, so bacterial laccase has a better application prospect industrial.
The existence of laccase in bacterium mainly contains three kinds of forms, that is: in extracellular laccase, cell, laccase becomes laccase with groups of cells.The enzyme of three kinds of forms of this that obtains, the Activity and stabill of enzyme is different.Obtain because intracellular enzyme needs broken wall, the enzymic activity reduction in broken born of the same parents' process of the laccase of this form is more obvious, and along with the broken various cell components of cell mix with laccase, also can bring difficulty to the purifying of enzyme; By comparison, advantage is apparent for two kinds of form laccases in addition, especially groups of cells becomes laccase, the bacterium of gemma Pseudomonas normally, because bacterial spore has stronger resistance to multiple unfavorable factors such as high temperature, high pressure, extreme pH and high salt, this kind laccase can show because of the characteristic of this special tectonic of gemma better temperature stability and pH stability.
Along with the development of Protocols in Molecular Biology, numerous laccase genes has obtained the clone and has analysed in depth.The expression and regulation mechanism of research laccase encoding gene helps to illustrate different genes role in developmental process, in addition, can also transform laccase gene by technology such as site-directed mutagenesises, improves laccase industrial application performance.
Dyestuff is widely used in the industries such as weaving, printing and dyeing, leather, the whole world is annual produce ten thousand kinds of dyestuffs after, the dyestuff that has 10-15% at least, does great damage to the ecotope of water body in physical environment by discharge of wastewater.Mostly the synthetic dyestuff of industrial application are aromatics, complex structure, difficult degradation.The treatment process of waste water from dyestuff mainly contains physico-chemical processes and biological treatment at present, and materialization treatment technology expense is high, has secondary pollution, and biological process becomes because of its economic environmental protection the method for administering preferably.Wherein laccase is owing to having substrate-function scope widely, but the dyestuff of catalyzed degradation various structures has application prospect preferably on industrial dye waste water is processed.Existing much about the research of the laccases decolouring dyestuff of using whiterot fungi or other originated from fungus, but less at the research report aspect dye decolored about bacterial laccase and bacterial laccase-mediator system.By the decolorizing effect of research bacterial laccase to different synthetic dyestuff, can further promote the industrial application of bacterial laccase.
Summary of the invention
The object of the invention is to provide a kind of bacillus amyloliquefaciens (Bacillus amyloliquefaciens) LC02, the present invention also aims to simultaneously provide a kind of bacillus amyloliquefaciens (Bacillusamyloliquefaciens) LC02 to produce the preparation method of gemma laccase, and a kind of method of utilizing the gemma laccase decolouring synthetic dyestuff of bacillus amyloliquefaciens (Bacillus amyloliquefaciens) LC02 product is provided.
Bacillus amyloliquefaciens provided by the invention (Bacillus amyloliquefaciens) LC02 has been preserved in (No. 3, Yard 1, BeiChen xi Road, Chaoyang District, Beijing City, China Committee for Culture Collection of Microorganisms's common micro-organisms center on October 22nd, 2010, Institute of Microorganism, Academia Sinica), deposit number is CGMCCNo.4258.
Above-mentioned Bacillus amyloliquefaciens strain is the forest topsoil separation acquisition from forest farm, Baolong shop, Heilongjiang Province of China Wuchang City.Bacillus amyloliquefaciens LC02 bacterial strain Gram-positive is given birth to amphitrichous in gemma.On solid Luria-Bertani (LB) substratum, cultivate 24h for 37 ℃, the little yellow of bacterium colony, protuberance are rounded, bacterium colony surface drying, smooth, it is lobate that colony edge is, the opaque and positive and negative solid colour of bacterium colony.The optimum growth temperature of bacterial strain is 37 ℃, and the most suitable growth pH is 6.0, can tolerate the NaCl of 1%-13%.
The invention provides bacillus amyloliquefaciens LC02 and produce the product spore culture medium formula of gemma laccase and the preparation method of gemma laccase.
Above-mentioned product spore culture medium prescription (g/L) is: nutrient broth 8; KCl 1; MgSO
47H
2O 0.25; MnCl
24H
2O 0.002; Agar 17; Transfer autoclave sterilization after pH7.0, add the 0.5mmol/LCaCl of filtration sterilization
2And 0.001mmol/L FeSO
4
The preparation method of above-mentioned gemma laccase is:
1) bacillus amyloliquefaciens LC02 streak inoculation is produced on the spore substratum in solid, after 5d is cultivated in 37 ℃ of inversions.
2) with aseptic deionized water, the gemma on solid medium is rinsed.
3) add the N,O-Diacetylmuramidase of final concentration 0.1mg/mL, 37 ℃ of water-bath 10min.
4) successively with the 1mol/L NaCl that contains 10mmol/L EDTA and 0.3mg/mL PMSF, 0.14mol/L NaCl and 0.1% (w/v) SDS cleans one time.
5) clean one time with aseptic deionized water.
6) clean three times with aseptic deionized water after 80 ℃ of water-bath thermal shock 10min.
7) get a certain amount of suspension after, with all the other suspensions pack into the sterilization after triangular flask in, 4 ℃ keep in Dark Place.
8) suspension that takes out is placed in 80 ℃ of baking ovens dries to constant weight, calculate gemma suspension concentration (mg/ml), and record.
The gemma laccase that bacillus amyloliquefaciens LC02 of the present invention produces can play a role in pH value 2.2-10.0 scope, and the optimum pH of the different substrates of catalysis is different: during take ABTS as substrate, enzyme is lived the highest when pH4.0; During take syringaldazine as substrate, enzyme is lived the highest when pH6.6; When being substrate with 2,6-syringol, enzyme is lived the highest when pH7.6.The gemma laccase that bacillus amyloliquefaciens LC02 of the present invention produces has stability preferably under alkaline condition, 30 ℃ of insulations active basic not loss in 5 days under the condition of pH10.0, can keep still after 10 days that initial enzyme lives 62.95%.These characteristics are that most fungal laccases are not available, because paper industry much adopts alkaline process, make paper waste alkalescence higher, and this gemma laccase fabulous stability under alkaline condition is conducive to it and brings into play useful effect in the processing such as paper waste.
The enzymatic reaction temperature range of the gemma laccase that bacillus amyloliquefaciens LC02 of the present invention produces is wider, its optimum temperuture is 70 ℃, can keep higher activity between 50-90 ℃, be 66.7% of the highest enzyme work in the time of 90 ℃, even still can keep 42.7% of the highest enzyme work under the high temperature of 100 ℃, fungal laccase completely loses activity substantially at this temperature.Simultaneously, this gemma laccase has thermostability preferably, and after insulation 10h under 50 ℃, 60 ℃ and 70 ℃, its enzyme work is respectively 69.1%, 40.17% and 17.63% of initial activity, and remnant enzyme activity is 20.14% after 80 ℃ of insulation 4h.This gemma laccase at high temperature satisfactory stability has a very large actual application value industrial.Metallic cation has larger impact to the activity of described laccase, as Na
+, K
+, Li
+, Mg
2+, Zn
2+, Ca
2+, Fe
3+And Al
3+Its activity there is activation, and Cu
2+, Mn
2+And Hg
2+Work has restraining effect to enzyme, wherein Hg
2+Can make gemma laccase complete deactivation of the present invention.Gemma laccase activity change under the NaCl of different concns that bacillus amyloliquefaciens LC02 of the present invention produces is larger, 0.1mol/L following NaCl has promoter action to the activity of described gemma laccase, 0.2mol/L NaCl activity is not had impact substantially, still can keep 42.12% of original activity when concentration exists up to the NaCl of 1mol/L.
The gemma laccase that bacillus amyloliquefaciens LC02 of the present invention produces has decolorization preferably to the industrial synthetic dyestuff of different chemical structures.In the presence of amboceptor Syringylethanone, when pH6.6 to RBBR (Remazol Brilliant Blue R, the gorgeous blue R of thunder agate element, CAS No:2580-78-1), the percent of decolourization after reactive black KN-B (CAS No:17095-24-8), isatin (CAS No:860-22-0) and Viola crystallina (CAS No:548-62-9) 6h is respectively 65.81%, 75.71%, 77.75% and 80.98%.When pH9.0, the percent of decolourization after RBBR, reactive black KN-B, isatin and Viola crystallina 6h is respectively 73.75%, 84.28%, 83.5% and 80.98%, illustrates that this gemma laccase has still kept higher decoloring ability to various dyestuffs under alkaline environment.This gemma laccase comprises the gorgeous blue R of thunder agate element to the synthetic dyestuff of different structure, reactive black KN-B, Viola crystallina and isatin decolour, and decolorization condition is: 40 ℃, and pH6.6 or 9.0, the final concentration of gemma laccase suspension is 1mg/mL, the dyestuff final concentration is respectively the gorgeous blue R 100mg/L of thunder agate element, reactive black KN-B 40mg/L, isatin 25mg/L, Viola crystallina 5mg/L, adding final concentration is the laccase amboceptor Syringylethanone of 0.1mmol/L.
Bacillus amyloliquefaciens laccase gene provided by the present invention comes from bacillus amyloliquefaciens LC02, and CGMCC No.4258 is one of following nucleotide sequences:
1) DNA sequence dna of SEQ ID No:1 in sequence table;
2) polynucleotide of SEQ ID No:2 protein sequence in the code sequence list;
3) DNA sequence dna that limits with sequence table SEQ ID No:1 has the homology 90% or more, and the identical function protein DNA sequence of encoding.
The present invention also relates to polypeptide, it has laccase activity and coded by the nucleic acid molecule of above-mentioned definition.The invention further relates to polypeptide, its aminoacid sequence is identical or homology with the aminoacid sequence of SEQ ID No:2 in the above described manner.
Bacillus amyloliquefaciens provided by the present invention (Bacillus amyloliquefaciens) LC02 can prepare the gemma suspension with laccase activity through fermentation culture, and this preparation method is simple to operate, and cost is lower.Prepared gemma laccase has pH and temperature catalysis scope widely, has preferably stablely under alkalescence and hot conditions, has more superior suitability than the laccase of originated from fungus.In the presence of amboceptor material Syringylethanone, this gemma laccase can effectively decolour to the synthetic dyestuff of different chemical structures, still kept decolorizing effect preferably under alkaline condition, therefore gemma laccase provided by the invention has application prospect preferably in the processing of industrial dye waste water.
Description of drawings
Fig. 1 is the impact of pH on bacillus amyloliquefaciens LC02 gemma laccase activity during take ABTS as substrate;
Fig. 2 is the impact of pH on bacillus amyloliquefaciens LC02 gemma laccase activity during take syringaldazine as substrate;
Fig. 3 is the impact of pH on bacillus amyloliquefaciens LC02 gemma laccase activity when being substrate with 2,6-syringol;
Fig. 4 is bacillus amyloliquefaciens LC02 gemma laccase enzyme under pH10.0 time history plot alive;
Fig. 5 is that differing temps is on the impact of bacillus amyloliquefaciens LC02 gemma laccase activity;
Fig. 6 is the stability of bacillus amyloliquefaciens LC02 gemma laccase activity in the time of 50-80 ℃;
Fig. 7 is that the NaCl of different concns is on the impact of bacillus amyloliquefaciens LC02 gemma laccase activity;
When Fig. 8 is pH6.6 bacillus amyloliquefaciens LC02 gemma laccase take Syringylethanone as amboceptor to the decolouring result of RBBR, reactive black KN-B, isatin and Viola crystallina
When Fig. 9 is pH9.0 bacillus amyloliquefaciens LC02 gemma laccase take Syringylethanone as amboceptor to the decolouring result of RBBR, reactive black KN-B, isatin and Viola crystallina
Embodiment
Following embodiment is in order to understand better the present invention.
Test materials used in following examples if no special instructions, is the biochemical reagents that can buy.Wherein bacterial genomes is extracted test kit and glue to reclaim test kit is Omega company product, and T carrier and other toolenzymes etc. are TaKaRa company product.
Said enzyme liquid in following embodiment is all bacillus amyloliquefaciens LC02 gemma laccases of preparing according to gemma laccase preparation method.
The enzyme activity determination method refers to calculate laccase activity with absorbancy after spectrophotometer detection laccase and substrate reactions.Described substrate is syringaldazine, and 2,2-azine-two (3-ethyl benzothiazole-6-sulfonic acid) (ABTS) or 2,6-syringol.
It is that the required enzyme amount of product is an enzyme activity unit that the activity of enzyme is defined as per minute oxidation 1 μ mol substrate.Reaction system is as follows:
(1) ABTS: reaction system contains 1mmol/L ABTS, 100 μ L gemma suspensions, and citric acid-phosphate buffered saline buffer (0.1mol/L, pH 3.0), cumulative volume 3mL, after 30 ℃ of reaction 3min at 420nm place mensuration light absorption value.
(2) syringaldazine: reaction system contains the 0.1mmol/L syringaldazine, 100 μ L gemma suspensions, and citric acid-phosphate buffered saline buffer (0.1mol/L, pH 7.0), cumulative volume 3mL, after 30 ℃ of reaction 3min at 525nm place mensuration light absorption value.
(3) 2,6-syringol: the system of answering contains 2mmol/L 2, the 6-syringol, 100 μ L gemma suspensions, and citric acid-phosphate buffered saline buffer (0.1mol/L, pH 7.0), cumulative volume 3mL, after 30 ℃ of reaction 5min at 468nm place mensuration light absorption value.
The character of embodiment 1 bacillus amyloliquefaciens LC02 gemma laccase
1.pH the impact of value on gemma laccase activity and stability
PH adopts pH2.2-7.8 citric acid-phosphate buffered saline buffer (0.1mol/L), pH7.4-9.0Tris-HCl (0.05mol/L) damping fluid and pH8.6-10.0 glycine-sodium hydrate buffer solution (0.05mol/L) to measure on the impact of laccase activity, pH on the impact of laccase stability by 30 ℃ the time with laccase and pH3.0, citric acid-phosphate buffered saline buffer of 8.0, measure remaining activity after mixing placement 1-10d in the Tris-HCl damping fluid of pH9.0 and pH10.0 glycine-sodium hydrate buffer solution.Fig. 1-3 show, gemma Laccase Catalyzed provided by the invention is in extensive range, but all catalytic substrate reactions in the scope of pH2.2-10.0, and with ABTS, the optimal pH that syringaldazine and 2,6-syringol record when being substrate is respectively 4.0,6.6 and 7.6.Fig. 4 shows, bacillus amyloliquefaciens LC02 gemma laccase has better stability in the environment of pH10.0, still can keep higher activity after 10d.
2. the impact of temperature on gemma laccase activity and stability
Temperature is being measured in 20-100 ℃ of scope under optimal pH the impact of laccase activity.The thermal stability determination of laccase is measured remaining activity after 50-80 ℃ of placement 0-10h in citric acid-phosphate buffered saline buffer of pH6.6.Fig. 5 shows, the optimal reactive temperature of bacillus amyloliquefaciens LC02 gemma laccase is 70 ℃, as can be seen from Figure 6, still can keep the approximately activity of 18% left and right even bacillus amyloliquefaciens LC02 gemma laccase is incubated 10h under 70 ℃ of high temperature.
3. the impact of metal ion on the gemma laccase activity
Add respectively common metal ion in reaction system, making its final concentration is 10mmol/L, at 30 ℃ of insulation 5min, take the reaction system that do not add metal ion as blank, then surveys according to a conventional method enzymic activity take syringaldazine as substrate.
4.NaCl the impact on the gemma laccase activity
Bacillus amyloliquefaciens LC02 gemma laccase is evenly mixed with the NaCl solution of different concns, measure remaining activity take syringaldazine as substrate after 30 ℃ of incubation 5min.Fig. 7 result shows, the following NaCl of 0.1mol/L has promoter action to bacillus amyloliquefaciens LC02 gemma laccase activity, and activity descends gradually when concentration increases.When NaCl concentration rose to 1mol/L, activity still can keep 42% left and right.
The decolouring of embodiment 2 bacillus amyloliquefaciens LC02 gemma laccases to synthetic dyestuff
1. the calculating of the reaction system of decolorization experiment and percent of decolourization
The experiment reaction system is 6mL, adds successively pH 6.6 citric acids-phosphate buffered saline buffer (0.1mol/L), dyestuff (kind and final concentration see Table 1), bacillus amyloliquefaciens LC02 gemma laccase (final concentration is 1mg/mL) and Syringylethanone (final concentration is 0.1mmol/L) in system.Simultaneously take the reaction system that do not add bacillus amyloliquefaciens LC02 gemma laccase as blank.Timing sampling, 12000rpm surveys the light absorption value under each dyestuff maximum absorption wavelength (seeing Table 1) after centrifugal 2min.All are measured equal triplicate and average.Calculate afterwards dye decolored rate.The percent of decolourization calculation formula of dyestuff is (A
0-A)/A
0* 100%, A wherein
0Be initial dyestuff light absorption value, A is the light absorption value that regularly sampling is surveyed.
Table 1 dye type, final concentration and maximum absorption wavelength
Result shows, bacillus amyloliquefaciens LC02 gemma laccase demonstrates the ability of stronger decolouring dyestuff.In the presence of amboceptor Syringylethanone, through the percent of decolourization of the synthetic dyestuff of four kinds of different structures after 6h decolouring all more than 65%, wherein to the percent of decolourization of Viola crystallina up to 80.98% (Fig. 8).
2. the decolorization experiment of dyestuff under alkaline condition
Because the advantage of bacterial laccase is to have the catalytic activity higher than fungal laccase under alkaline condition, for further investigate bacterial laccase in alkaline environment to the decoloring ability of dyestuff, select the condition research bacillus amyloliquefaciens LC02 gemma laccase of pH9.0 to the decolouring of four kinds of synthetic dyestuff.Through after 6h, the percent of decolourization of RBBR, reactive black KN-B, isatin and Viola crystallina is respectively 73.75%, 84.28%, 83.5% and 80.98%, this result is higher than the percent of decolourization of various dyestuffs under pH6.6, show that this gemma laccase has still kept higher decoloring ability to various dyestuffs under alkaline environment, have suitability preferably when processing the waste water from dyestuff of different pH values.
The clone of embodiment 3 bacillus amyloliquefaciens LC02 gemma laccase genes
1. the clone of bacterial strain laccase gene
Above-mentioned bacterial strains is chosen to 5mL LB liquid nutrient medium, 37 ℃, 200rpm, overnight incubation.Extract with reference to Omega company bacterial genomes the genomic dna that the test kit specification sheets extracts above-mentioned bacterial strains, and detect through 1% agarose gel electrophoresis.
The employing genomic dna is template, with upstream primer " CGG
GAATTCGGCACTGGAAAAATTTGCAGATG " (restriction enzyme site EcoR I) and downstream primer " CCG
CTCGAGTTACTGCTTATCCGTGACGTCC " (restriction enzyme site Xho I) amplification bacterial strain bacillus amyloliquefaciens LC02 gemma laccase gene.
Add following reagent: ddH in 200 μ L PCR pipes
2O 13.75 μ L, 10 * Ex Taq Buffer2 μ L, 10mmol/L dNTP mixture 1 μ L, 10 μ mol/L upstream primer 1 μ L, 10 μ mol/L downstream primer 1 μ L, DNA profiling 1 μ L, Ex Taq enzyme 0.25 μ L, cumulative volume 20 μ L.Negative control is set simultaneously.The PCR reaction conditions: 94 ℃ of 4min denaturations, 94 ℃ of 45s, 53 ℃ of 45s, 72 ℃ of 2min, 30 circulations, 72 ℃ of 10min extend.Amplified production detects through 1% agarose gel electrophoresis.
Go out the purpose fragment of capacity by pcr amplification, downcut the purpose band after 1% agarose gel electrophoresis separates, reclaim test kit with Omega company glue and reclaim the purpose fragment with reference to specification sheets.The purity of the purpose fragment that reclaims detects with 1% agarose gel electrophoresis.
2. connect T carrier and conversion
1) follow these steps to add reaction solution: pMD18-T vector1 μ L, glue reclaims product 3 μ L, ddH
2O 1 μ L, Solution I 5 μ L, cumulative volume 10 μ L, 16 ℃ of ligation 1h.
2) E.coli JM109 competent cell is melted in ice.
3) 10 μ L ligation liquid are joined in 100 μ L competent cells, inhale gently and beat mixing, ice bath 30min, 42 ℃ of insulation 60s, ice bath 5min.
4) add 890 μ L LB liquid nutrient mediums, 200rpm cultivates 1h for 37 ℃.Negative control is set simultaneously.
5) get appropriate above-mentioned nutrient solution and be evenly coated on the LB/Amp/X-Gal/IPTG flat board, 37 ℃ of overnight incubation.
3. the screening and identification of restructuring T carrier
1) by the positive transformant of blue hickie screening white, white colony is chosen to the 5mLLB/Amp liquid nutrient medium, 37 ℃, 200rpm, overnight incubation.
2) extract plasmid with reference to specification sheets with plasmid extraction kit from the bacterium liquid of incubated overnight.
3) PCR identifies.
Add successively following reagent: ddH
2O 13.75 μ L, 10 * Taq Buffer, 2 μ L, 10mmol/LdNTP mixture 1 μ L, 10 μ mol/L upstream primer 1 μ L, 10 μ mol/L downstream primer 1 μ L, plasmid template 1 μ L, Taq enzyme 0.25 μ L, cumulative volume 20 μ L.Negative control is set simultaneously.The PCR reaction conditions: 94 ℃ of 4min denaturations, 94 ℃ of 45s, 53 ℃ of 45s, 72 ℃ of 2min,, 30 circulations, 72 ℃ of 10min extend.Amplified production detects through 1% agarose gel electrophoresis.
4) enzyme is cut evaluation.
Add successively following reagent: 10 * H Buffer, 2 μ L, EcoR I 1 μ L, Xho I 1 μ L, plasmid 3 μ L, ddH
2O 13 μ L, cumulative volume 20 μ L.37 ℃ of reaction 3h.1% agarose gel electrophoresis detects enzyme and cuts product.
4. the order-checking of laccase gene and sequential analysis
PCR and enzyme are cut detected correct positive colony and be sent to the order-checking of Shanghai Ying Jun biotech company, sequencing result is seen sequence table SEQ ID No:1.
Claims (7)
1. bacillus amyloliquefaciens (Bacillus amyloliquefaciens) LC02, the deposit number at China Committee for Culture Collection of Microorganisms's common micro-organisms center is CGMCC No.4258.
2. gemma laccase, this laccase is produced by bacillus amyloliquefaciens CGMCC No.4258 claimed in claim 1, and the gene of this gemma laccase is the DNA sequence dna shown in SEQ ID NO:1.
3. gemma laccase claimed in claim 2, is characterized in that, the aminoacid sequence of this enzyme is the sequence shown in SEQ ID NO:2.
4. according to claim 2 or 3 described gemma laccases, it is characterized in that, this gemma laccase plays a role at pH 2.2～10.0, the optimum pH of catalytic substrate ABTS is 4.0 in the time of 30 ℃, the optimum pH of catalytic substrate syringaldazine is 6.6, catalytic substrate 2, the optimum pH of 6-syringol are 7.6.
5. according to claim 2 or 3 described gemma laccases, is characterized in that, this gemma laccase is 20-100 ℃ of performance function, pH 6.6 during take syringaldazine as substrate optimal reactive temperature be 70 ℃.
6. according to claim 2 or 3 described gemma laccases, it is characterized in that, this gemma laccase comprises the gorgeous blue R of thunder agate element to the synthetic dyestuff of different structure, reactive black KN-B, Viola crystallina and isatin decolour, decolorization condition is: 40 ℃, pH 6.6 or 9.0, the final concentration of gemma laccase suspension is 1mg/mL, the dyestuff final concentration is respectively the gorgeous blue R 100mg/L of thunder agate element, reactive black KN-B 40mg/L, isatin 25mg/L, Viola crystallina 5mg/L, adding final concentration is the laccase amboceptor Syringylethanone of 0.1mmol/L.
7. the preparation method of according to claim 2 or 3 described gemma laccases is characterized in that following these steps to carrying out:
A. bacillus amyloliquefaciens CGMCC No.4258 streak inoculation is produced on the spore substratum in solid, and after 5d was cultivated in 37 ℃ of inversions, described product spore media components was: nutrient broth 8g/L; KCl 1g/L; MgSO
47H
2O 0.25g/L; MnCl
24H
2O0.002g/L; Agar 17g/L; Transfer autoclave sterilization after pH7.0, add the 0.5mmol/L CaCl of filtration sterilization
2And 0.001mmol/L FeSO
4
B. with aseptic deionized water, the gemma on solid medium is rinsed;
C. the N,O-Diacetylmuramidase that adds final concentration 0.1mg/mL, 37 ℃ of water-bath 10min;
D. clean one time with the 1mol/L NaCl, the 0.14mol/L NaCl that contain 10mmol/L EDTA and 0.3mg/mL PMSF, 0.1%w/v SDS and aseptic deionized water successively;
E.80 after cleaning three times with aseptic deionized water after ℃ thermal shock 10min, in the triangular flask after the sterilization of packing into, 4 ℃ keep in Dark Place.
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| CN110218708B (en) * | 2019-06-20 | 2021-08-27 | 天津科技大学 | Bacterial laccase and gene, preparation method and application thereof |
| CN113173647B (en) * | 2021-04-26 | 2022-10-25 | 河北农业大学 | Bacillus amyloliquefaciens MN-13 and application thereof |
| CN113462701B (en) * | 2021-09-03 | 2021-11-26 | 佛山市玉凰生态环境科技有限公司 | High-temperature polyphenol oxidase and application thereof in treatment of phenol-containing wastewater |
| CN114350554A (en) * | 2021-12-29 | 2022-04-15 | 西南科技大学 | Preparation and application method of radioactive decontamination strippable membrane biodegradation microbial inoculum |
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