CN103409382B - A kind of strengthen the technology of lignin degradation in Phanerochaete chrysosporium solid fermentation - Google Patents
A kind of strengthen the technology of lignin degradation in Phanerochaete chrysosporium solid fermentation Download PDFInfo
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Abstract
The present invention is a kind of strengthens the technology of lignin degradation in Phanerochaete chrysosporium solid fermentation, relates to bioengineering field.This technical characteristic is straw through pulverizing, with containing proper amount of hydrogen peroxide etc. pretreating process, then the Phanerochaete chrysosporium strain of lignin degrading is accessed, the degraded of solid fermentation degrading straw lignin can be strengthened, and cellulose is seldom degraded.This technical matters is easy, will not be to environment, also will not waste of resources is caused.The straw using the method processing can be used as preparing bio-ethanol and the raw material of butanol and as biological feedstuff, and is favorably improved the value of straw.
Description
Technical field
The present invention relates to bioengineering field, refer in particular to hydrogen peroxide pretreatment without high temperature, the straw of HIGH PRESSURE TREATMENT, strengthen Phanerochaete chrysosporium solid fermented straw lignin degradation, the technology of suppression cellulose degradation.
Background technology
The energy is the important substance basis of economy and social development.Since the industrial revolution, world's fossil energy consumption is rapid, and ecological environment constantly deteriorates, and particularly greenhouse gas emission causes increasingly serious Global climate change, and the sustainable development of human society is by serious threat.Since the seventies in last century, the idea of sustainable development progressively becomes international community's common recognition, regenerative resource develops to be paid much attention to by countries in the world, many countries will develop the regenerative resource important component part as energy strategy, propose clear and definite Renewable Energy Development target, having formulated law and the policy encouraging Renewable Energy Development, regenerative resource is developed rapidly.At present, China has become world energy sources production and consumption big country, but per capita energy's level of consumption is the lowest.Along with the economic and development of society, China's energy demand is by sustainable growth.Increase energy supply, the sustainable development ensureing energy security, preserving the ecological environment, facilitate economic and social, be a great strategic task of China's economy and social development.Regenerative resource is the energy resources that China is important, meet energy demand, improve energy resource structure, reduce environmental pollution, the aspect such as promote economic development has played important function.Wherein the exploitation of biomass energy is an importance of regenerative resource.And be the importance that biomass energy is developed with cellulose raw material producing fuel ethyl alcohol by ferment or other biological fuel.But cellulose raw material exists content and is only second to the lignin of content of cellulose; it is wrapped in around cellulose with crystal form; protection cellulose is not easy to be degraded by microorganism or enzyme preparation, is therefore how to destroy the lignin in cellulose raw material with the topmost problem of the existence of cellulose raw material fermenting and producing bio-fuel.
Destroy the main method of lignin in straw at present and have 5 kinds of methods such as steam-explosion pretreatment, sulfur acid pretreatment, NaOH pretreatment, pretreatment with agueous Ammonia and Biological Pretreatment.These methods are generally owing to investment is big, cost is high, secondary pollution problems, and are difficult to industrialized production.The patent and the existing substantial amounts of report such as patent (application number/patent No.: 200810064332) of paper that utilize biodegradation straw lignin in recent years describe strengthening white rot fungus secretion manganese peroxidase enzyme method, the method is advanced by three days than the method for existing fermented by white rot fungus manganese peroxidase, fermentation period shortens half, and production of enzyme is higher than 900U/L；Patent (application number: 200680022879) target is to increase white rot basidiomycetes and produces Extracellular laccase and the yield of manganese peroxidase, and reduces cost, and the method, relative to existing culture technique, can make laccase and manganese peroxidase production of enzyme dramatically increase；Patent (application number: 200910079781) describes another kind of manganese peroxidase producing strains Trichoderma harzianum, this bacterium (4-5 days) can form a large amount of conidium in a short time, its conidial speed of formation is fast about week age than Phanerochaete chrysosporium, and sporiparous ability can reach 10 times of Phanerochaete chrysosporium, Phanerochaete chrysosporium is then the strain that in basidiomycetes, growth is stronger with sporiparous ability；The weak point aiming to overcome that current white rot fungus degrading lignin of patent (application number: 200610109413), and the microbial bacterial agent of a kind of novel lignin degrading and the method utilizing above-mentioned microbial inoculum lignocellulose degradation are provided.
But these patented technologies have a common problem to be exactly biological when lignin degrading, how to control the degraded of cellulose, because cellulose is the primary raw material of biofermentation ethanol, the degraded only controlling cellulose during Biological Pretreatment could improve the yield of the fuel such as bio-ethanol, butanol.
The present inventor, through in-depth study, finds out a kind of with straw as primary raw material, by the method for lignin in Phanerochaete chrysosporium solid culture degrading straw.The method is used strain Phanerochaete chrysosporium strain with method difference in the past, uses straw as primary raw material, by lignin in solid fermentation degrading straw, controls the degraded of cellulose simultaneously.
Summary of the invention
One purpose of the present invention there is provided a kind of with Phanerochaete chrysosporium as strain, by controlling the degradation technique of cellulose while solid fermentation degrading straw lignin, use the fermented product obtained by this technology fermented stalk for fermenting organism fuel, such as ethanol and butanol, the yield of bio-fuel can be improved greatly.
A kind of strengthen the technology of lignin degradation in Phanerochaete chrysosporium solid fermentation, with Phanerochaete chrysosporium as starting strain, fermented stalk raw material, carry out test tube amplification culture, liquid submerged culture, first order seed cultivates and solid fermentation is cultivated, and obtains the Phanerochaete chrysosporium solid fermentation thing containing manganese peroxidase.
Strain used by the present invention is Phanerochaete chrysosporium any one strain (Phanerochaete chrysosporium), such as the strain of China General Microbiological culture presevation administrative center (CCGMC), Chinese agriculture Microbiological Culture Collection administrative center (ACCC), Chinese industrial Microbiological Culture Collection administrative center (CICC), Chinese medicine Microbiological Culture Collection administrative center (CMCC), National Veterinary Culture Collection (CVCC) and antibiotic strain preservation pipe reason center etc. preservation.
Raw material used in the present invention is any one straw, agricultural crop straws containing lignin as all in corn straw, rice straw, Wheat Straw, broomcorn straw, soybean stalk, cotton stalk etc., and straw first passes around pulverizing, crosses the sieve of 20～100 mesh.
First class inoculum culture medium of the present invention is: wheat bran and water are in 1:0.5～3(mass ratio) ratio mixing, pH is natural, subpackage 500mL triangular flask, every bottle 80～200g, 110～135 DEG C of sterilizings 30～180 minutes.
Two grades expand bacterium culture medium is corn cob with water in 1:0.5～4(mass ratio) ratio mixing, it is subsequently adding corn cob and the 0 of water gross weight～5% soybean cake powder, 0～5% Semen Maydis pulp (mass ratio), mix homogeneously, pH is natural, 110～130 DEG C of sterilizings 30～180 minutes.
Wherein said solid-state fermentation culture medium is: straw, hydrogen peroxide and water press 1:0.2～1:0.5～4(mass ratio) mix homogeneously, react 3～24 hours, add corn cob, hydrogen peroxide and the 0 of water gross weight～5% soybean cake powder, 0～5% Semen Maydis pulp (mass ratio), it is fermentation medium.
Wherein said first class inoculum culture process is, inoculates a ring Phanerochaete chrysosporium test tube slant spore in the 250mL triangular flask equipped with 20～100g first class inoculum culture medium, 20～50 DEG C, quiescent culture 24～120 hours；Wherein said second class inoculum amplification culture technique is that first class inoculum is inoculated on two grades of expansion bacterium culture mediums in the ratio (strain and two grades of expansion bacterium culture medium weight ratios) of 1:5～100, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 4～40cm, expecting wide 0.5～2 meter, length does not limits, and ventilation is 0.3～1.5:1(gas volume/fermentation medium weight)/minute, incubation time is 3～23 days, halfway stirring 1～2 times.
The wherein said degradable fermented technique of straw lignin controlling cellulose degradation is: second class inoculum is inoculated in solid fermentation culture medium in the ratio (strain and solid fermentation culture medium weight ratio) of 1:5～100, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 4～40cm, expecting wide 0.5～2 meter, length does not limits, and ventilation is 0.3～1.5:1(gas volume/fermentation medium weight)/minute, incubation time is 10 days～60 days, halfway stirring 1～5 times.Use this technique to use solid fermentation, and raw material is without high temperature high pressure process, so will not give environment, also will not waste resource.Lignin degradation rate can reach 75～98%, cellulose degradation rate 0～2%.
The fermented product after this Technology degrading straw lignin is used to may be used for the raw material of the bio-fuel such as fermenting alcohol, butanol.
In order to material technical scheme involved by and technique are expanded on further, give following example, but these embodiments limit the scope of the present invention the most in any form.
Detailed description of the invention
The mensuration of content of lignin sees the analysis of Yang Sheng chief editor's " forage analysis and determination of feeds quality technology " (the 1st edition) chapter 4 cellulose and measures.Lignin degradation rate calculates and presses Tsang
Deng method:
Embodiment 1
1, the making of test tube slant strain
At newly configured potato sucrose culture medium (" the industrial microorganism experimental technique handbook " of Zhu Gejian, Wang Zhengxiang chief editor, 1994, page 367) the middle ring Phanerochaete chrysosporium strain (China General Microbiological culture presevation administrative center CCGMC5.776) that accesses, 26 DEG C, incubation time 50 hours；4 DEG C save backup.
2, first class inoculum makes
Wheat bran and water are in 1:0.5(mass ratio) ratio mixing, pH naturally, subpackage 500mL triangular flask, every bottle of 200g, 135 DEG C of sterilizings 30 minutes；A ring Phanerochaete chrysosporium test tube slant spore is inoculated after cooling, 21 DEG C, quiescent culture 115 hours.
3, prepared by two grades of expansion strains
Corn cob and water are in 1:0.5(mass ratio) ratio mixing, be subsequently adding 5% soybean cake powder of corn cob and water gross weight, 5% Semen Maydis pulp (mass ratio), mix homogeneously, pH naturally, 110 DEG C of sterilizings 170 minutes；In ratio (strain and two grades of expansion bacterium culture medium weight ratios) the inoculation first class inoculum of 1:5, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 38cm, expecting wide 0.5 meter, length does not limits, and ventilation is 1.45:1(gas volume/fermentation medium weight)/minute, incubation time is 22 days, halfway stirring 2 times.
4, solid fermentation degrading straw lignin
Straw, hydrogen peroxide and water press 1:0.2:3.9(mass ratio) mix homogeneously, reacts 23 hours, adds corn cob, hydrogen peroxide and 4.8% soybean cake powder of water gross weight, 0.1% Semen Maydis pulp (mass ratio), be fermentation medium；Second class inoculum is inoculated in solid fermentation culture medium in the ratio (strain and solid fermentation culture medium weight ratio) of 1:98, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 39cm, expecting wide 0.5 meter, length does not limits, and ventilation is 0.32:1(gas volume/fermentation medium weight)/minute, incubation time is 9 days, halfway stirring 1 time.
5, after fermentation ends, analyze the weight-loss ratio in lignin and content of cellulose, and sweat, 76% can be reached through being calculated Lignin degradation rate, cellulose degradation rate 0.2%.
Embodiment 2
1, the making of test tube slant strain
A ring Phanerochaete chrysosporium strain (Chinese agriculture Microbiological Culture Collection administrative center ACCC is accessed in newly configured potato sucrose culture medium (" the industrial microorganism experimental technique handbook " of Zhu Gejian, Wang Zhengxiang chief editor, page 1994,367)
30942), 26 DEG C, incubation time 50 hours；4 DEG C save backup.
2, first class inoculum makes
Wheat bran and water are in 1:1.8(mass ratio) ratio mixing, pH naturally, subpackage 500mL triangular flask, every bottle of 132g, 124 DEG C of sterilizings 117 minutes；A ring Phanerochaete chrysosporium test tube slant spore is inoculated after cooling, 36 DEG C, quiescent culture 68 hours.
3, prepared by two grades of expansion strains
Corn cob and water are in 1:2.6(mass ratio) ratio mixing, be subsequently adding 2.3% soybean cake powder of corn cob and water gross weight, 2.2% Semen Maydis pulp (mass ratio), mix homogeneously, pH naturally, 124 DEG C of sterilizings 100 minutes；In ratio (strain and two grades of expansion bacterium culture medium weight ratios) the inoculation first class inoculum of 1:48, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 24cm, expecting wide 1.2 meters, length does not limits, and ventilation is 0.8:1(gas volume/fermentation medium weight)/minute, incubation time is 12 days, halfway stirring 2 times.
4, solid fermentation degrading straw lignin
Straw, hydrogen peroxide and water press 1:0.6:2.6(mass ratio) mix homogeneously, reacts 13 hours, adds corn cob, hydrogen peroxide and 2.5% soybean cake powder of water gross weight, 2.8% Semen Maydis pulp (mass ratio), be fermentation medium；Second class inoculum is inoculated in solid fermentation culture medium in the ratio (strain and solid fermentation culture medium weight ratio) of 1:58, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 25cm, expecting wide 1.3 meters, length does not limits, and ventilation is 1.8:1(gas volume/fermentation medium weight)/minute, incubation time is 38 days, halfway stirring 3 times.
5, after fermentation ends, analyze the weight-loss ratio in lignin and content of cellulose, and sweat, 85% can be reached through being calculated Lignin degradation rate, cellulose degradation rate 1.12%.
Embodiment 3
1, the making of test tube slant strain
A ring Phanerochaete chrysosporium strain (Chinese industrial Microbiological Culture Collection administrative center is accessed in newly configured potato sucrose culture medium (" the industrial microorganism experimental technique handbook " of Zhu Gejian, Wang Zhengxiang chief editor, page 1994,367)
CICC14067), 26 DEG C, incubation time 50 hours；4 DEG C save backup.
2, first class inoculum makes
Wheat bran and water are in 1:2.9(mass ratio) ratio mixing, pH naturally, subpackage 500mL triangular flask, every bottle of 83g, 110 DEG C of sterilizings 170 minutes；A ring Phanerochaete chrysosporium test tube slant spore is inoculated after cooling, 48 DEG C, quiescent culture 25 hours.
3, prepared by two grades of expansion strains
Corn cob and water are in 1:3.9(mass ratio) ratio mixing, be subsequently adding 0% soybean cake powder of corn cob and water gross weight, 0% Semen Maydis pulp (mass ratio), mix homogeneously, pH naturally, 130 DEG C of sterilizings 32 minutes；In ratio (strain and two grades of expansion bacterium culture medium weight ratios) the inoculation first class inoculum of 1:97, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 4.5cm, expecting wide 1.8 meters, length does not limits, and ventilation is 0.4:1(gas volume/fermentation medium weight)/minute, incubation time is 3 days, halfway stirring 1 time.
4, solid fermentation degrading straw lignin
Straw, hydrogen peroxide and water press 1:0.9:0.5(mass ratio) mix homogeneously, reacts 4 hours, adds corn cob, hydrogen peroxide and 0.1% soybean cake powder of water gross weight, 4.5% Semen Maydis pulp (mass ratio), be fermentation medium；Second class inoculum is inoculated in solid fermentation culture medium in the ratio (strain and solid fermentation culture medium weight ratio) of 1:6, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 4cm, expecting wide 2 meters, length does not limits, and ventilation is 1.5:1(gas volume/fermentation medium weight)/minute, incubation time is 56 days, halfway stirring 5 times.
5, after fermentation ends, analyze the weight-loss ratio in lignin and content of cellulose, and sweat, 98% can be reached through being calculated Lignin degradation rate, cellulose degradation rate 2%.
Claims (1)
1. strengthening a method for lignin degradation in Phanerochaete chrysosporium solid fermentation, its feature is being carried out as steps described below: the making of (1) test tube slant strain
A ring Phanerochaete chrysosporium CGMCC5.776 strain is accessed in newly configured potato sucrose culture medium, 26 DEG C, incubation time 50 hours；4 DEG C save backup；
(2) first class inoculum makes
Wheat bran and the water ratio of 1:0.5 in mass ratio mix, and pH is natural, subpackage 500mL triangular flask, every bottle of 200g, 135 DEG C of sterilizings 30 minutes；A ring Phanerochaete chrysosporium test tube slant spore is inoculated after cooling, 21 DEG C, quiescent culture 115 hours；
(3) two grades expand strain and prepare
Corn cob and the water ratio of 1:0.5 in mass ratio mix, and are subsequently adding 5% soybean cake powder of corn cob and water gross weight, the Semen Maydis pulp of mass ratio meter 5%, mix homogeneously, and pH is natural, 110 DEG C of sterilizings 170 minutes, are two grades and expand bacterium culture mediums；The ratio inoculation first class inoculum that bacterium culture medium weight ratio is 1:5 is expanded in strain and two grades, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 38cm, expecting wide 0.5 meter, length does not limits, according to the ventilation of gas volume/fermentation medium weight be (1.45:1)/minute, incubation time is 22 days, halfway stirring 2 times；
(4) solid fermentation degrading straw lignin
Corn cob, hydrogen peroxide and water are 1:0.2:3.9 mix homogeneously in mass ratio, react 23 hours, add corn cob, hydrogen peroxide and 4.8% soybean cake powder of water gross weight, and mass ratio is 0.1% Semen Maydis pulp, is solid fermentation culture medium；Second class inoculum is inoculated in solid fermentation culture medium in the ratio of strain Yu solid fermentation culture medium weight ratio 1:98, mix homogeneously, it is laid on solid fermentation bed cultivation, compost thickness 39cm, expecting wide 0.5 meter, length does not limits, ventilation according to the ratio of gas volume and fermentation medium weight be (0.32:1)/minute, incubation time is 9 days, halfway stirring 1 time；
(5) after fermentation ends, analyze the weight-loss ratio in lignin and content of cellulose, and sweat, reach 76% through being calculated Lignin degradation rate, cellulose degradation rate 0.2%.
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| CN103784479B (en) * | 2014-01-20 | 2017-01-04 | 湖南大学 | Phanerochaete chrysosporium antioxidation extracting solution and preparation method thereof |
| CN103789279B (en) * | 2014-01-20 | 2016-08-17 | 湖南大学 | Phanerochaete chrysosporium extracting solution containing antioxidase and preparation method |
| CN104946702A (en) * | 2015-02-11 | 2015-09-30 | 河南农业大学 | Method for pretreating lignocellulose raw material by combining ferric chloride and white rot fungi |
| CN105255953B (en) * | 2015-10-09 | 2018-12-25 | 淮阴工学院 | Physical-chemical-Biological Pretreatment corn stover method |
| CN110226489B (en) * | 2019-06-27 | 2022-05-03 | 深圳市铁汉生态环境股份有限公司 | Slope greening spray-seeding fiber matrix material and preparation method and use method thereof |
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