CN102399710A - Brevibacillus laterosporus, microorganism strain agent and microorganism fertilizer prepared by using brevibacillus laterosporus as well as preparation methods thereof - Google Patents
Brevibacillus laterosporus, microorganism strain agent and microorganism fertilizer prepared by using brevibacillus laterosporus as well as preparation methods thereof Download PDFInfo
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Abstract
The invention relates to a novel brevibacillus laterosporus which has the collection number of CGMCC (China General Microbiological Culture Collection Center) No.5090, a microorganism strain agent and a microorganism fertilizer prepared by using the strain as well as preparation methods thereof. According to the strain provided by the invention, the produced microorganism strain agent has the advantages of higher effective microbial content and longer quality guarantee period.
Description
Technical field
The present invention relates to a kind of new bacillus laterosporus and microbial strains agent and microbial fertilizer and their preparation method who prepares by this bacterial strain.
Background technology
China has a large population, ploughs few, and along with successively decreasing year by year in population growth, industry and development of city arable land.According to the statistics made by the departments concerned, China's population increases by 1,600 ten thousand every year on average, and 4,000,000 mu of the annual minimizings of ploughing.Nineteen fifty population 5.5 hundred million, plough 16.5 hundred million mu, 2.99 mu of per capita cultivated lands, the per capita cultivated land was 1.51 mu in 1980, the nineteen ninety per capita cultivated land drops to 1.1 mu, is significantly less than 4.03 mu of world per capita cultivated lands' level, also is lower than 2.1 mu of Asia per capita cultivated lands' level.For this reason, unique feasible way of China's increase agricultural output is to increase the yield per unit area.Could satisfy industrial development and population increases the demand to agricultural-food, and chemical fertilizer is also with regard to the natural widespread use that obtained.
The soil compaction that unreasonable for a long time use chemical fertilizer brings, soil fertility decline, ecological damage, environmental pollution and agricultural byproducts quality decline problem have received the great attention of national departments concerned and agricultural science and technology circle.Using in a large number of chemical fertilizer caused soil fertility decline, the disadvantage that soil compaction and agriculture production cost improve constantly.In recent decades, China makes great efforts to explore the rational application of fertilizer always, overcomes the drawback of chemical fertilizer and the effective way of raising chemical fertilizer utilization ratio.
Agricultural fertilizer comprises chemical fertilizer and bio-feritlizer, is the irreplaceable important production means of China's agriculture prodn.Wherein, bio-feritlizer is as the important branch of agro-biological engineering subject and the important component part of soil fertilizer science, develops rapidly all having obtained aspect fundamental research and the applied research in nearly ten years.And the microbial fertilizer in the agricultural fertilizer (belonging to a kind of of bio-feritlizer) more and more is familiar with by people as a kind of important effect of agrotechnical measure in the development an agriculture featuring high yields, fine quality and high efficiency; This provides sizable development space for its exploitation, popularization, application; Particularly the irreplaceability in development Organic farming, production A level, AA level green food has demonstrated fully its potential glamour.
China's microbial fertilizer development in recent years is very fast, has many enterprises to be engaged in production and operation, and kind constantly increases, and also has some external products to squeeze into the home market simultaneously.Owing to reasons such as bacterial classifications, the quality product of existing market is uneven, has occurred some problems in the production application.According to Ministry of Agriculture's random checking recent years, tracking selective examination, the situation of country's system inspection is seen, spot-check qualification rate less than 60%, and product quality problem mainly is that effective bacterium number is not up to standard, and the quality guaranteed period is too short.Living bacteria count is the important indicator of quality product in the microbial fertilizer; Living bacteria count is not up to standard, and quality product just can not get guaranteeing that what reflect is that effect is unstable; Wherein reason mainly is the bacterial classification problem; Bacterial classification is after being prepared as the microbial strains agent, and the survival ability in preserving process descends, and the survival time shortens.This problem is actually owing to the employed bacterial classification of these microbial strains agent or can not produces gemma; The ability that produces gemma is more weak, and the gemma that perhaps produces is sprouted ability, can not finely tide over stress conditions and stock, preserving process in the microbial strains agent production process; In the production use, showing as bacterial activity descends; Production performance weakens, and reproduction speed is slack-off, and resistance is poor.Therefore, the bacterial classification problem perplexs the production and the development of China's microbial fertilizer always.
Summary of the invention
The bacterial classification survival ability is low in the prior art, living bacteria count is not up to standard in order to solve, the quality guaranteed period is too short, thus problems such as quality product is relatively poor, effect instability, and one of the object of the invention provides a kind of new bacillus laterosporus.
Two of the object of the invention provides a kind of microbial strains agent by the preparation of this bacillus laterosporus and preparation method thereof.
Three of the object of the invention provides a kind of microbial fertilizer that is prepared from this microbial strains agent and preparation method thereof.
Novel bacterial provided by the invention can very well solve the strain number problem that prolongs with the quality guaranteed period up to standard with the microbial strains agent that utilizes this bacterial classification production, and this makes the present invention seem very important and meaningful.
Per-cent of mentioning among the present invention and ratio all are meant weight percent and part by weight.
In order to achieve the above object, the present invention provides following technical scheme:
A kind of new bacillus laterosporus (Bacillus laterosporus), preserving number is CGMCC No.5090.Concrete, this bacterial classification is named as " new lateral bud spore bacillus No. 1 ", and this strain separating is from high-yielding grain fields, and through domestication, proterties is stable for a long time.
The biological characteristics of this bacterial classification is that thalline is shaft-like, belongs to bacillus, and its cell size is 0.15～0.18 * 215～510um; Gram-positive; Can be changed into feminine gender, gemma is oval, adnation, middle life or nearly middle giving birth to; Sporangiocyst expands, and free gemma is on one side than the other side thick (canoe shape).Can utilize multiple nitrogenous source, carbon source, growth temperature 20-55 ℃, 37 ℃ of optimum growth temps, optimal pH 7.2.Under bad condition, thalline transforms and produces gemma, and gemma can tolerate mal-conditions such as 100 ℃ of high temperature 20 minutes and drying to the poor environment strong stress resistance.
New No. 1 bacterial strain of lateral bud spore bacillus is submitted China Committee for Culture Collection of Microorganisms's common micro-organisms center preservation on July 22nd, 2010; Deposit number is CGMCC No.5090; Biology name Bacillus laterosporus; Depositary institution address: No. 3, Yard 1, BeiChen xi Road, Chaoyang District, Beijing City, Institute of Microorganism, Academia Sinica.
The present invention also require to protect a kind of microbial strains agent by this strain preparation with and preparation method thereof.Specific as follows:
The substratum that is used among the present invention has:
New No. 1 substratum (slant medium): peptone 5g/L, sodium-chlor 5g/L, Carnis Bovis seu Bubali cream 5g/L, agar 1.5%-2.0%, PH transfers to 6.5-7.8.
New No. 1 liquid nutrient medium: this substratum does not contain agar, and other compositions are identical with new 1 substratum with content, and PH transfers to 6.5-7.8.
New No. 2 substratum: starch 5g/L, sucrose 1g/L, Yeast diffusion juice 0.2g/L, peptone 5g/L, Carnis Bovis seu Bubali cream 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sal epsom 0.2g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8.
New No. 3 substratum: starch 10g/L, sucrose 5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 10g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8.
New No. 4 substratum: starch 10g/L, sucrose 2.5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8.
More than all substratum all before use through high pressure steam sterilization (121 ℃, 1.1kg/cm
3, 30 minutes), cooling.
The present invention also can adopt substratum and the cultural method used in traditional microbial strains agent production to prepare the microbial strains agent.
Substratum and cultural method that traditional microbial strains agent is used in producing have detailed description in the bacterial classification catalogue at China Committee for Culture Collection of Microorganisms common micro-organisms center.
The concrete working method of microbial strains agent:
One, culture presevation and activation culture
Bacterial classification is gone up preservation with streak culture mode at new 1 substratum (slant medium), and the short term storage condition is 4 ℃, per activation in February 1 time; Long-term storage conditions is-20 ℃, and activation was 1 time in per 6 months.
Two, microorganism culturing
1, adopt method provided by the invention to carry out microorganism culturing:
1) preserve the inclined-plane certainly and get kind after, line inserts slant medium (new 1 substratum), 30-38 ℃ of incubators left standstill dark condition under cultivation 36 hours;
2) use the aseptic water washing inclined-plane, form bacteria suspension;
3) 1 volume bacteria suspension is inserted in new 1 liquid nutrient medium of about 20 volumes, it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
4) bacteria suspension that step 3) is obtained joins in new 2 substratum of about 5-10 times volume, and it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
5) bacteria suspension that step 4) is obtained joins in new 3 substratum of about 50-100 times volume, and it is 10 that 35-38 ℃ of aerobic is cultured to cell concentration
8Individual/the ml order of magnitude;
6) bacteria suspension that step 5) is obtained joins in new 4 substratum of about 5-10 times volume, and it is 10 that 35-38 ℃ of cultivation aerobic is cultured to cell concentration
9Individual/the ml order of magnitude.
2, adopt traditional microbial fermentation production method to carry out microorganism culturing
Substratum: starch 10%, soybean cake powder 10%, potassium hydrogenphosphate 0.2%, ammonium sulfate 0.1%, sal epsom 0.05%, iron(ic)chloride 0.001%, lime carbonate 0.01%, yeast extract paste 0.01%, PH7.2-7.4.
With inserting in the above-mentioned substratum of 1000ml behind the actication of culture, triangular flask shakes a bottle 160RPM, cultivates 16 hours for 30-38 ℃; Be inoculated in the 200L seed fermentation jar by 1% inoculum size then and (still be substratum of the same race); Ventilation was cultivated 16 hours for 30-38 ℃, received in the 2000L fermentor tank by 10% inoculum size (still to be substratum of the same race) again; Cultivate for 30-38 ℃ and be warming up to 40-45 ℃ after 20 hours, treat to stop fermentation after 80% thalline produces gemma cultivation 10 hours.
Three, the production of microbial strains agent
High-quality peat composed of rotten mosses powder (commercially available) is carried out the dry sterilization postcooling; Join in the fermented liquid that fermentation ends (traditional microbial fermentation production method or working method provided by the invention) obtains according to the content of wanting to obtain mikrobe in the microbial strains agent; Fully stir, use the tablets press granulation, oven drying at low temperature; Be packaged into Kucheng and be microbial strains agent product, mixing with common chemical fertilizer or organic carrier as required during use to become microbial fertilizer.
Particularly, the mixed weight ratio of peat composed of rotten mosses powder and fermented liquid is 2-10:1, and preferred, blending ratio is 3-5:1, and is preferred, and blending ratio is 4:1.
Particularly, the common chemical fertilizer that is adopted is conventional nitrogen, phosphorus, potassic fertilizer, and the mixed weight ratio of microbial strains agent and common chemical fertilizer is 1:5-15, and preferred, blending ratio is 1:8-10.The organic carrier that is adopted can be this area fertilizer commonly used, can adopt chicken manure, ground corn core, crushing straw, cinder etc.Specifically can adopt chicken manure, ground corn core, cinder, three's blending ratio is 1:1-5:1-6, and preferred three's blending ratio is 1:2:3.The mixed weight ratio of microbial strains agent and organic carrier is 1:5-15, and preferred, blending ratio is 1:7-10, preferred 1:9.
Useful effect
Use the microbial strains agent of bacterial classification production provided by the present invention that higher effective bacterium number and long quality guaranteed period are arranged.
Use the traditional zymotic mode to carry out the inoculum agent of fermentative prodn at this bacterial classification, carry out effective bacterium number during warehouse-in and detect, its result obviously is superior to the effective bacterium number in commercially available other microbial strains agent, and effective bacterium number is 3.3 times of national standard.Solved strain number problem not up to standard.
The inoculum agent warehouse-in that uses fermentation mode provided by the invention to carry out fermentative prodn at this bacterial classification the time carries out effective bacterium number and detects, and its result obviously is superior to the effective bacterium number in commercially available other microbial strains agent, and effectively the bacterium number is 4 times of national standard.Also solved strain number problem not up to standard.
The inoculum agent that this bacterial classification uses the traditional zymotic mode to carry out fermentative prodn is preserved 2 years in the warehouse after, carry out effective bacterium number and detect, its result obviously is superior to the effective bacterium number in commercially available other microbial strains agent, and effective bacterium number is 3 times of national standard.Solved short problem of quality guaranteed period.
The inoculum agent that this bacterial classification uses fermentation mode provided by the invention to carry out fermentative prodn is preserved 2 years in the warehouse after, carry out effective bacterium number and detect, its result obviously is superior to the effective bacterium number in commercially available other microbial strains agent, and effective bacterium number is 3.6 times of national standard.Solved short problem of quality guaranteed period.
Embodiment
Embodiment 1: utilize traditional method that new side is carried out the agent of fermentative prepn microbial strains for No. 1
Substratum: starch 3%, soybean cake powder 1%, peptone 0.1%, ammonium sulfate 0.2%, potassium hydrogenphosphate 0.2%, yeast powder 0.1%, lime carbonate 0.01%, PH7.2-7.4.
With inserting behind the actication of culture in the above-mentioned substratum of 1000ml; Triangular flask shakes bottle 160RPM and cultivated 16 hours for 37 ℃, is inoculated in the 200L seed fermentation jar by 1% inoculum size then (still to be substratum of the same race), ventilation; Cultivated 16 hours for 37 ℃; Receive (still being substratum of the same race) in the 2000L fermentor tank by 10% inoculum size again, cultivate for 37 ℃ and be warming up to 42 ℃ after 20 hours, treat to stop fermentation after 80% thalline produces gemma cultivation 10 hours.Detect cell concentration, reach 10
9, the weight percent by 1:4 mixes with the high-quality peat composed of rotten mosses powder (commercially available) that carries out the dry sterilization postcooling then, carries out granulation again, and oven drying at low temperature becomes the microbial strains agent.
Embodiment 2: utilize method provided by the invention that new side is carried out the agent of fermentative prepn microbial strains for No. 1
Earlier bacterial classification is carried out activation, use 5ml aseptic water washing inclined-plane again, form bacteria suspension, bacteria suspension inserts the 500ml triangular flask; This triangular flask contains new 1 liquid nutrient medium of 100ml, uses shaking table to cultivate 18 hours, and culture condition is 37 ℃; 180-200rpm detects cell concentration, reaches 10 in concentration
8The order of magnitude carries out next step;
100ml bacterium liquid in the 500ml triangular flask is transferred in the 2000ml triangular flask, and this triangular flask contains new 2 substratum of 700ml, uses shaking table to cultivate 20 hours, and culture condition is 37 ℃, 180-200rpm; Detect cell concentration, reach 10 in concentration
8The order of magnitude carries out next step;
Bacterium liquid in the 2000ml triangular flask is inserted 1m
3In the fermentor tank, the access amount is 6 liters, contains new 3 substratum of 500L in this fermentor tank, and fermentation condition is: temperature 36-38 ℃, and tank pressure 0.5kg/cm, air flow 20m
3/ h cultivated 8 hours; Detect cell concentration, reach 10 in concentration
8The order of magnitude carries out next step;
With 1m
3Bacterium liquid in the fermentor tank inserts 5m
3Fermentor tank, access amount are 500 liters, and this fermentor tank contains 3m
3New 4 substratum, fermentation condition is: temperature 36-38 ℃, tank pressure 0.5kg/cm, air flow 120m
3/ h cultivated 15 hours.Detect cell concentration, reach 10 in concentration
9The order of magnitude stops fermentation.Mix with the high-quality peat composed of rotten mosses powder (commercially available) that carries out the dry sterilization postcooling in the ratio of 1:4 then, carry out granulation again, oven drying at low temperature becomes the microbial strains agent.
Embodiment 3: the microbial strains agent to utilizing the traditional method preparation is not being carried out the detection of bacterium number under stock's the condition for a long time
Dilution plate number scale according to routine detects the viable bacteria content in the microbial strains agent.Take by weighing microbial strains agent 1 gram (stock's two weeks); With the sterilized water dissolving, using sterilized water to be diluted to the thalline number is 20-100/ml, pipettes the 1ml diluent then in sterile petri dish; Add an amount of new 1 substratum (slant medium); The thorough mixing after coagulation is inverted in 37 ℃ of insulation cans and was cultivated 48 hours, the bacterium colony on the statistics flat board; More than the triplicate, multiply by this gram microbial strains dilution agent with MV is the strain number that the milliliter number of cell concentration when being 20-100/ml is the agent of every gram microbial strains.We are not carrying out the detection of bacterium number under stock's the condition for a long time to the microbial strains agent that utilizes the traditional method preparation, and detected result is 6.6*10
8Individual/gram, (national standard is 2.0*10 for 3.3 times of national standard
8Individual/gram).Solved inoculum agent microbe number problem not up to standard.
Embodiment 4: the microbial strains agent to utilizing method preparation provided by the invention is not being carried out the detection of bacterium number under stock's the condition for a long time
Dilution plate number scale according to routine detects the viable bacteria content in the microbial strains agent.Take by weighing microbial strains agent 1 gram (stock's two weeks); With the sterilized water dissolving, using sterilized water to be diluted to the thalline number is 20-100/ml, pipettes the 1ml diluent then in sterile petri dish; Add an amount of new 1 substratum (slant medium); The thorough mixing after coagulation is inverted in 37 ℃ of insulation cans and was cultivated 48 hours, the bacterium colony on the statistics flat board; More than the triplicate, multiply by this gram microbial strains dilution agent with MV is the strain number that the milliliter number of cell concentration when being 20-100/ml is the agent of every gram microbial strains.We are not carrying out the detection of bacterium number under stock's the condition for a long time to the microbial strains agent that utilizes method preparation provided by the invention, and detected result is 8*10
8Individual/gram, be 4 times of national standard.Solved inoculum agent microbe number problem not up to standard.
Embodiment 5: the bacterium number is carried out in the microbial strains agent that utilizes the traditional method preparation detect under long-time stock's condition
Dilution plate number scale according to routine detects the viable bacteria content in the microbial strains agent.Take by weighing microbial strains agent 1 gram (stock 2 years); With the sterilized water dissolving, using sterilized water to be diluted to the thalline number is 20-100/ml, pipettes the 1ml diluent then in sterile petri dish; Add an amount of new 1 substratum (slant medium); The thorough mixing after coagulation is inverted in 37 ℃ of insulation cans and was cultivated 48 hours, the bacterium colony on the statistics flat board; More than the triplicate, multiply by this gram microbial strains dilution agent with MV is the strain number that the milliliter number of cell concentration when being 20-100/ml is the agent of every gram microbial strains.We carry out the detection of bacterium number to the microbial strains agent that utilizes the traditional method preparation under long-time stock's (2 years) condition, detected result is 6*10
8Individual/gram, be 3 times of national standard.Solved inoculum agent microbe number problem and the too short problem of preservation term not up to standard.
Embodiment 6: the bacterium number is carried out in the microbial strains agent that utilizes method preparation provided by the invention detect under long-time stock's condition
Dilution plate number scale according to routine detects the viable bacteria content in the microbial strains agent.Take by weighing microbial strains agent 1 gram (stock 2 years); With the sterilized water dissolving, using sterilized water to be diluted to the thalline number is 20-100/ml, pipettes the 1ml diluent then in sterile petri dish; Add an amount of new 1 substratum (slant medium); The thorough mixing after coagulation is inverted in 37 ℃ of insulation cans and was cultivated 48 hours, the bacterium colony on the statistics flat board; More than the triplicate, multiply by this gram microbial strains dilution agent with MV is the strain number that the milliliter number of cell concentration when being 20-100/ml is the agent of every gram microbial strains.We carry out the detection of bacterium number to the microbial strains agent that utilizes method preparation provided by the invention under long-time stock's (2 years) condition, detected result is 7.2*10
8Individual/gram, be 3.6 times of national standard.Solved inoculum agent microbe number problem and the too short problem of preservation term not up to standard.
Embodiment 7: the microbial strains agent of lengthy warehousing does not mix the effect that use the back with fertilizer
Chicken manure, ground corn core, cinder are mixed with the 1:2:3 weight ratio; The adjustment water cut is 30%; Piled up 7-10 days under in temperature, mix the microbial strains agent of stock's two weeks with the weight ratio of 1:9 with it, process microbial fertilizer greater than 30 ℃ condition.
The microbial fertilizer of processing is carried out on Different Crop and the fertile and of equal value conventional fertile sub-district fertilizer efficiency experiment relatively of matrix, 0.16 mu of each sub-district area, 3 repetitions are established in experiment.Execute 25 kilograms of microbial fertilizers for every mu during experiment; Matrix fertile (mix with the 1:2:3 weight percent via chicken manure, ground corn core, cinder, after the adjustment water cut is 30%, piles up under greater than 30 ℃ condition in temperature and to process in 7-10 days) is executed 25 kilograms for every mu; Conventional fertile (phosphoric acid diamino: urea: Repone K is that 3:3:2 mixes) of equal value executed 25 kilograms for every mu.All, once executed, do not appended as base manure.Blank does not apply fertilizer.
Experimental result is (data are the raising the output per-cent of each fertilizer with respect to blank) as follows
| ? | Romaine lettuce | Sponge gourd | Corn | Paddy rice | Peanut | Cucumber |
| Microbial fertilizer | 14 | 25 | 15 | 14 | 17 | 30 |
| Matrix is fertile | 1 | 19 | 10 | 9 | 10 | 25 |
| Of equal value conventional fertile | 3 | 18 | 8 | 5 | 11 | 17 |
The result shows that this microbial strains agent can finely play a role, and has good effect of increasing production.
Embodiment 8: the microbial strains agent of lengthy warehousing (2 years) mixes the effect that use the back with fertilizer
Chicken manure, ground corn core, cinder are mixed with the 1:2:3 weight ratio; The adjustment water cut is 30%; Piled up 7-10 days under in temperature, mix the microbial strains agent in 2 years of stock with the weight ratio of 1:9 with it, process microbial fertilizer greater than 30 ℃ condition.
The microbial fertilizer of processing is carried out on Different Crop and the fertile and of equal value conventional fertile sub-district fertilizer efficiency experiment relatively of matrix, 0.16 mu of each sub-district area, 3 repetitions are established in experiment.Execute 25 kilograms of microbial fertilizers for every mu during experiment; Matrix fertile (mix with the 1:2:3 weight percent via chicken manure, ground corn core, cinder, after the adjustment water cut is 30%, piles up under greater than 30 ℃ condition in temperature and to process in 7-10 days) is executed 25 kilograms for every mu; Conventional fertile (phosphoric acid diamino: urea: Repone K is that 3:3:2 mixes) of equal value executed 25 kilograms for every mu.All, once executed, do not appended as base manure.Blank does not apply fertilizer.
Experimental result is (data are the raising the output per-cent of each fertilizer with respect to blank) as follows
| ? | Romaine lettuce | Wheat | Corn | Tomato | Cotton | Cucumber |
| Microbial fertilizer | 7 | 12 | 13 | 32.5 | 11.8 | 30 |
| Matrix is fertile | 1 | 7 | 9 | 9 | 8 | 25 |
| Of equal value conventional fertile | 3 | 7 | 8 | 16 | 6 | 18 |
The result shows that this microbial strains agent can be good at solving the quality guaranteed period problem, on result of use, do not have marked difference by the fertilizer of its preparation with respect to the fertilizer of the microbial strains agent preparation of prolonged preservation not, has solved the present invention and has wanted the problem that solves.
Claims (10)
1. a bacillus laterosporus (Bacillus laterosporus) is characterized in that its preserving number at China Committee for Culture Collection of Microorganisms common micro-organisms center is CGMCC No.5090.
2. bacillus laterosporus microbial strains agent is characterized in that this inoculum agent is got with the turfy soil mixing granulation through cultivation and fermentation by bacillus laterosporus then.
3. bacillus laterosporus microbial strains according to claim 2 agent is characterized in that this microbial strains agent is prepared from following method:
1) line of CGMCC No.5090 bacterial strain is inserted slant medium (new 1 substratum), 30-38 ℃ of incubators leave standstill under the dark condition to be cultivated 36 hours;
2) use the aseptic water washing inclined-plane, form bacteria suspension;
3) 1 volume bacteria suspension is inserted in new 1 liquid nutrient medium of 20 volumes, it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
4) bacteria suspension that step 3) is obtained joins in new 2 substratum of 5-10 times of volume, and it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
5) bacteria suspension that step 4) is obtained joins in new 3 substratum of 50-100 times of volume, and it is 10 that 35-38 ℃ of aerobic is cultured to cell concentration
8Individual/the ml order of magnitude;
6) bacteria suspension that step 5) is obtained joins in new 4 substratum of 5-10 times of volume, and it is 10 that 35-38 ℃ of cultivation aerobic is cultured to cell concentration
9Individual/the ml order of magnitude, stop fermentation; Mix with turfy soil in the ratio of 1:2-10 then, granulation, oven drying at low temperature obtains the microbial strains agent;
Wherein above-mentioned substratum is: new No. 1 substratum (slant medium): peptone 5g/L, and sodium-chlor 5g/L, Carnis Bovis seu Bubali cream 5g/L, agar 1.5%-2.0%, PH transfers to 6.5-7.8,
New No. 1 liquid nutrient medium: this substratum does not contain agar, and other compositions are identical with new 1 substratum with content, and PH transfers to 6.5-7.8,
New No. 2 substratum: starch 5g/L, sucrose 1g/L, Yeast diffusion juice 0.2g/L, peptone 5g/L, Carnis Bovis seu Bubali cream 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sal epsom 0.2g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8,
New No. 3 substratum: starch 10g/L, sucrose 5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 10g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8,
New No. 4 substratum: starch 10g/L, sucrose 2.5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8.
4. bacillus laterosporus microbial strains according to claim 2 agent is characterized in that this microbial strains agent is prepared from following method:
With inserting the 1000ml substratum after the activation of CGMCC No.5090 bacterial strain: starch 10%, soybean cake powder 10%, potassium hydrogenphosphate 0.2%, ammonium sulfate 0.1%; Sal epsom 0.05%, iron(ic)chloride 0.001%, lime carbonate 0.01%, yeast extract paste 0.01%; Among the PH7.2-7.4, triangular flask shakes a bottle 160RPM, cultivates 16 hours for 30-38 ℃; Be inoculated into (still being above-mentioned substratum of the same race) in the 200L seed fermentation jar by 1% inoculum size then, ventilation was cultivated 16 hours for 30-38 ℃; Receive (still being above-mentioned substratum of the same race) in the 2000L fermentor tank by 10% inoculum size again, cultivate for 30-38 ℃ and be warming up to 40-45 ℃ after 20 hours, treat to stop fermentation after 80% thalline produces gemma cultivation 10 hours; Mix with turfy soil in the ratio of 1:2-10 then, granulation, oven drying at low temperature obtains the microbial strains agent.
5. microbial fertilizer is characterized in that this fertilizer is mixed by one of claim 2-4 described bacillus laterosporus microbial strains agent and common fertilizer and/or organic carrier.
6. microbial fertilizer according to claim 5, wherein said common fertilizer are nitrogenous fertilizer, phosphate fertilizer and/or potash fertilizer, and described organic carrier is chicken manure, ground corn core and/or cinder.
7. method of producing the microbial strains agent is characterized in that concrete steps are following:
1) line of CGMCC No.5090 bacterial strain is inserted slant medium (new 1 substratum), 30-38 ℃ of incubators leave standstill under the dark condition to be cultivated 36 hours;
2) use the aseptic water washing inclined-plane, form bacteria suspension;
3) 1 volume bacteria suspension is inserted in new 1 liquid nutrient medium of 20 volumes, it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
4) bacteria suspension that step 3) is obtained joins in new 2 substratum of 5-10 times of volume, and it is 10 that 30-38 ℃ of aerobics are cultured to cell concentration
8Individual/the ml order of magnitude;
5) bacteria suspension that step 4) is obtained joins in new 3 substratum of 50-100 times of volume, and it is 10 that 35-38 ℃ of aerobic is cultured to cell concentration
8Individual/the ml order of magnitude;
6) bacteria suspension that step 5) is obtained joins in new 4 substratum of 5-10 times of volume, and it is 10 that 35-38 ℃ of cultivation aerobic is cultured to cell concentration
9Individual/the ml order of magnitude, stop fermentation; Mix with turfy soil in the ratio of 1:2-10 then, granulation, oven drying at low temperature obtains the microbial strains agent;
Wherein above-mentioned substratum is: new No. 1 substratum (slant medium): peptone 5g/L, and sodium-chlor 5g/L, Carnis Bovis seu Bubali cream 5g/L, agar 1.5%-2.0%, PH transfers to 6.5-7.8,
New No. 1 liquid nutrient medium: this substratum does not contain agar, and other compositions are identical with new 1 substratum with content, and PH transfers to 6.5-7.8,
New No. 2 substratum: starch 5g/L, sucrose 1g/L, Yeast diffusion juice 0.2g/L, peptone 5g/L, Carnis Bovis seu Bubali cream 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sal epsom 0.2g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8,
New No. 3 substratum: starch 10g/L, sucrose 5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 10g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8,
New No. 4 substratum: starch 10g/L, sucrose 2.5g/L, Yeast diffusion juice 0.1g/L, peptone 0.5g/L, soybean cake powder 5g/L, ammonium sulfate 1g/L, potassium primary phosphate 0.5g/L, sodium-chlor 5g/L, PH transfers to 6.5-7.8,
More than all substratum all before use through high pressure steam sterilization (121 ℃, 1.1kg/cm
3, 30 minutes), cooling.
8. the method for microbial strains agent according to claim 7, the blending ratio that it is characterized in that fermented liquid and turfy soil is 1:4.
9. a method of producing the microbial strains agent is characterized in that concrete steps are following: with inserting the 1000ml substratum after the activation of CGMCC No.5090 bacterial strain: starch 10%, soybean cake powder 10%; Potassium hydrogenphosphate 0.2%, ammonium sulfate 0.1%, sal epsom 0.05%; Iron(ic)chloride 0.001%, lime carbonate 0.01%, yeast extract paste 0.01%; Among the PH7.2-7.4, triangular flask shakes a bottle 160RPM, cultivates 16 hours for 30-38 ℃; Be inoculated into (still being above-mentioned substratum of the same race) in the 200L seed fermentation jar by 1% inoculum size then, ventilation was cultivated 16 hours for 30-38 ℃; Receive (still being above-mentioned substratum of the same race) in the 2000L fermentor tank by 10% inoculum size again, cultivate for 30-38 ℃ and be warming up to 40-45 ℃ after 20 hours, treat to stop fermentation after 80% thalline produces gemma cultivation 10 hours; The part by weight of pressing 1:2-10 then mixes with turfy soil, granulation, and oven drying at low temperature obtains the microbial strains agent.
10. the method for microbial strains agent according to claim 9, the blending ratio that it is characterized in that fermented liquid and turfy soil is 1:4.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN106831015A (en) * | 2017-02-23 | 2017-06-13 | 麻林涛 | A kind of bacillus laterosporus microbial manure and its production and use |
| CN111733109A (en) * | 2020-07-15 | 2020-10-02 | 杨凌绿都生物科技有限公司 | Preparation and application of bacillus laterosporus microbial inoculum with growth promoting function |
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| CN1624110A (en) * | 2004-11-08 | 2005-06-08 | 麻林涛 | Phosphorus bacteria and process for producing microorganism manure strain agent using said bacteria |
| CN1624111A (en) * | 2004-11-08 | 2005-06-08 | 麻林涛 | Potassium bacteria and process for producing microorganism manure strain agent using said bacteria |
| CN1966670A (en) * | 2006-08-04 | 2007-05-23 | 东莞市保得生物工程有限公司 | Bacillus laterosporus and soil inoculation agent prepared from the strain |
| CN102101800A (en) * | 2009-12-17 | 2011-06-22 | 天津市施易得肥料有限公司 | Method for preparing microbial organic fertilizer |
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| CN1624110A (en) * | 2004-11-08 | 2005-06-08 | 麻林涛 | Phosphorus bacteria and process for producing microorganism manure strain agent using said bacteria |
| CN1624111A (en) * | 2004-11-08 | 2005-06-08 | 麻林涛 | Potassium bacteria and process for producing microorganism manure strain agent using said bacteria |
| CN1966670A (en) * | 2006-08-04 | 2007-05-23 | 东莞市保得生物工程有限公司 | Bacillus laterosporus and soil inoculation agent prepared from the strain |
| CN102101800A (en) * | 2009-12-17 | 2011-06-22 | 天津市施易得肥料有限公司 | Method for preparing microbial organic fertilizer |
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| CN106831015A (en) * | 2017-02-23 | 2017-06-13 | 麻林涛 | A kind of bacillus laterosporus microbial manure and its production and use |
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