CN101492484B - Synthetic circulation production process for guanine nucleoside - Google Patents

Synthetic circulation production process for guanine nucleoside Download PDF

Info

Publication number
CN101492484B
CN101492484B CN2009100427858A CN200910042785A CN101492484B CN 101492484 B CN101492484 B CN 101492484B CN 2009100427858 A CN2009100427858 A CN 2009100427858A CN 200910042785 A CN200910042785 A CN 200910042785A CN 101492484 B CN101492484 B CN 101492484B
Authority
CN
China
Prior art keywords
guanosine
membrane
mother liquor
filtration
liquid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN2009100427858A
Other languages
Chinese (zh)
Other versions
CN101492484A (en
Inventor
钟广新
蔡传康
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hunan Han Jing Rui amino acid Co., Ltd.
Original Assignee
HUNAN SECO BIOTECHNOLOGY CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by HUNAN SECO BIOTECHNOLOGY CO Ltd filed Critical HUNAN SECO BIOTECHNOLOGY CO Ltd
Priority to CN2009100427858A priority Critical patent/CN101492484B/en
Publication of CN101492484A publication Critical patent/CN101492484A/en
Application granted granted Critical
Publication of CN101492484B publication Critical patent/CN101492484B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • Y02P60/873

Landscapes

  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Saccharide Compounds (AREA)

Abstract

The invention provides a comprehensive recycling production process of guanosine. The bacterial suspension collected from the process in which guanosine is extracted and refined from guanosine fermented liquid is dried as feed additive or made into feed protein; the primary mother liquid acquired from the first four times during micro-filtrate membrane filtration, crude crystallization and pressure filtration and separation is sent into a reverse osmosis membrane for condensation and then mixed with the guanosine fermented liquid for internal recycling; the primary mother liquid acquired from the fifth time undergoes evaporation concentration, crystallization, drying and granulation to produce ammonium sulfate and other bio-compound fertilizers; the secondary mother liquid acquired from ultrafiltration membrane treatment is reused as micro-filtration membrane dialysis water; the third mother liquid acquired from extract crystallization and pressure filtration and separation is respectively reused as anti-crystallinic water of anti-crystallinic jar and dialysis water of micro-filtration membrane and ultrafiltration membrane. The invention overcomes the defects of the traditional process such as incomprehensive utilization, resources waste and environmental pollution; the comprehensive cycling process is reasonable and feasible and conforms to the green environmental protection concept, thus cleaning the environment, promoting the ecological balance, reducing the production cost and strengthening the social and economic benefits.

Description

A kind of synthetic circulation production process of guanosine-
Technical field
The present invention relates to produce the synthetic circulation production process of the production technique of guanosine-, particularly a kind of guanosine-.
Background technology
Guanosine-(guanosine) is the important intermediate of food and medical product, and its purposes is very extensive, and annual requirement is with the speed increase of 10%-20%.At present, the fermentative Production guanosine has been advanced production technique.The refining guanosine of extraction is generally slightly got from the guanosine fermented liquid, essence is got with separate three technological processs; Each leaching process all can produce bacteria suspension and residue mother liquor (claiming mother liquor, secondary mother liquid and three mother liquors again a time); These bacteria suspensions generally all do not carry out scientific and reasonable comprehensive utilization once more with the residue mother liquor; Waste precious resources, polluted environment.
Summary of the invention
To the deficiency of above-mentioned similar technology, the purpose of this invention is to provide a kind of to bacteria suspension and three kinds of guanosine-environmental protection production technique that mother liquor fully utilizes.
Technical scheme of the present invention is:
1, bacteria suspension comprehensive utilization:
Bacteria suspension oven dry with the guanosine fermented liquid produces after microfiltration membrane is handled both can be used as fodder additives, also can be made into feedstuff protein.
2, a mother liquor comprehensive utilization:
1. in the thick leaching process of guanosine; Through the guanosine stillness of night of micro-filtrate membrane filtration is stirred decrease temperature crystalline in the bullion crystallizer after; A mother liquor that obtains in the time of will separating with plate-and-frame filter press is sent into reverse osmosis membrane and is concentrated, and then sends into microfiltration membrane and mix with the guanosine fermented liquid and carry out internal recycle technology; 60 ℃ of the temperature of reverse osmosis membrane technology, pressure≤0.35Mpa, flow rate control is at 100L/m 2.h-200L/m 2.h, be concentrated into guanosine content and reach 15g/L-20g/L;
2. above-mentioned internal recycle technology is one-period with 5 times, and the mother liquor that the 5th obtains is concentrated to 5 times-6 times in temperature≤80 ℃, vacuum pressure under-0.06Mpa--0.08Mpa the condition through quadruple effect evaporator earlier; Again liquid concentrator is sent into continuous crystallizer continuous crystallisation under 85 ℃ of temperature, vacuum pressure-0.06Mpa--0.08Mpa condition, obtain inorganic salt crystal such as ammonium sulfate; Separate with the continuous cone centrifugal basket drier again, separating factor 2000, moisture is less than 25%-30%; Under 100 ℃, rotating speed 8r/min-12r/min condition, dry moisture 8%-10% with the tube bank dryer then; With the crystal granulation of tablets press to oven dry, granularity 1.5mm-2.5mm obtains ammonium sulfate and other bio-compound fertilizers at last at last.
3, secondary mother liquid comprehensive utilization:
Removing albumen, pigment through ultra-filtration membrane in the smart leaching process of guanosine, to handle the secondary mother liquid volume that the back obtains less, and pigment, impurity are more, and guanosine content 0.4g/L-0.5g/L can be all utilize as the microfiltration membrane water of dialysing again.
4, three mother liquor comprehensive utilizations:
The guanosine clear liquid of ultrafiltration membrance filter is after the elaboration crystallizer stirs decrease temperature crystalline; Three mother liquor volumes that obtain when separating with plate-and-frame filter press are big; Pigment, impurity are considerably less, and guanosine content 0.4g/L-0.5g/L can be respectively dissolves brilliant water and microfiltration membrane, the ultra-filtration membrane water of dialysing and utilize as dissolving brilliant jar.
Advantage of the present invention is: 1. fully fully utilize the bacteria suspension that obtains in the guanosine production process, mother liquor, secondary mother liquid and three mother liquors, meet the environmental protection new concept, purified environment, promoted the eubiosis; 2. resource effectively comprehensive utilization comprehensively on the basis that guanosine is produced, has been derived from fodder additives, feedstuff protein and composite bio-fertilizer addition product; 3. comprehensive circulation technology is reasonable, feasible, has reduced production cost, has strengthened the corporate social economic benefit.
Embodiment
Concrete production process of the present invention is:
1, bacteria suspension comprehensive utilization:
Bacteria suspension oven dry with the guanosine fermented liquid produces after microfiltration membrane is handled both can be used as fodder additives, also can be made into feedstuff protein.
2, a mother liquor comprehensive utilization:
1. in the thick leaching process of guanosine; Through the guanosine stillness of night of micro-filtrate membrane filtration is stirred decrease temperature crystalline in the bullion crystallizer after; A mother liquor that obtains in the time of will separating with plate-and-frame filter press is sent into reverse osmosis membrane and is concentrated, and then sends into microfiltration membrane and mix with the guanosine fermented liquid and carry out internal recycle technology; 60 ℃ of the temperature of reverse osmosis membrane technology, pressure≤0.35Mpa, flow rate control is at 100L/m 2.h-200L/m 2.h, be concentrated into guanosine content and reach 15g/L-20g/L;
2. above-mentioned internal recycle technology is one-period with 5 times, and the mother liquor that the 5th obtains is concentrated to 5 times-6 times in temperature≤80 ℃, vacuum pressure under-0.06Mpa--0.08Mpa the condition through quadruple effect evaporator earlier; Again with liquid concentrator send into continuous crystallizer in 85 ℃ of temperature, vacuum pressure for continuous crystallisation under the-0.06Mpa--0.08Mpa condition, obtain inorganic salt crystal such as ammonium sulfate; Separate with the continuous cone centrifugal basket drier again, separating factor 2000, moisture is less than 25%-30%; Under 100 ℃, rotating speed 8r/min-12r/min condition, dry moisture 8%-10% with the tube bank dryer then; With the crystal granulation of blade type tablets press to oven dry, granularity 1.5mm-2.5mm obtains ammonium sulfate and other bio-compound fertilizers at last at last.
3, secondary mother liquid comprehensive utilization:
Removing albumen, pigment through ultra-filtration membrane in the smart leaching process of guanosine, to handle the secondary mother liquid volume that the back obtains less, and pigment, impurity are more, and guanosine content 0.4g/L-0.5g/L can be all utilize as the microfiltration membrane water of dialysing again.
4, three mother liquor comprehensive utilizations:
The guanosine clear liquid of ultrafiltration membrance filter is after the elaboration crystallizer stirs decrease temperature crystalline; Three mother liquor volumes that obtain when separating with plate-and-frame filter press are big; Pigment, impurity are considerably less, and guanosine content 0.4g/L-0.5g/L can be respectively dissolves brilliant water and microfiltration membrane, the ultra-filtration membrane water of dialysing and utilize as dissolving brilliant jar.

Claims (1)

1. the bacteria suspension and residue mother liquor synthetic circulation production process that produce of a guanosine-leaching process is characterized in that:
(1), bacteria suspension comprehensive utilization:
Bacteria suspension oven dry with the guanosine fermented liquid produces after microfiltration membrane is handled both can be used as fodder additives, also can be made into feedstuff protein;
(2), a mother liquor comprehensive utilization:
1. in the thick leaching process of guanosine; Through the guanosine clear liquid of micro-filtrate membrane filtration stirs decrease temperature crystalline in the bullion crystallizer after; A mother liquor that obtains in the time of will separating with plate-and-frame filter press is sent into reverse osmosis membrane and is concentrated, and then sends into microfiltration membrane and mix with the guanosine fermented liquid and carry out internal recycle technology; 60 ℃ of the temperature of reverse osmosis membrane technology, pressure≤0.35Mpa, flow rate control is at 100L/m 2.h-200L/m 2.h, be concentrated into guanosine content and reach 15g/L-20g/L;
2. above-mentioned internal recycle technology is one-period with 5 times, and the mother liquor that the 5th obtains is concentrated to 5 times-6 times in temperature≤80 ℃, vacuum pressure under-0.06Mpa--0.08Mpa the condition through quadruple effect evaporator earlier; Again with liquid concentrator send into continuous crystallizer in 85 ℃ of temperature, vacuum pressure for continuous crystallisation under the-0.06Mpa--0.08Mpa condition, obtain ammonia sulfate crystal; Separate with the continuous cone centrifugal basket drier again, separating factor 2000, moisture is less than 25%-30%; Under 100 ℃, rotating speed 8r/min-20r/min condition, dry moisture 8%-10% with the tube bank dryer then; With the crystal granulation of tablets press to oven dry, granularity 1.5mm-2.5mm obtains composite bio-fertilizer ammonium sulfate at last at last;
(3), secondary mother liquid comprehensive utilization:
Removing albumen, pigment through ultra-filtration membrane in the smart leaching process of guanosine, to handle the secondary mother liquid volume that the back obtains less, and pigment, impurity are more, and guanosine content 0.4g/L-0.5g/L can be all utilize as the microfiltration membrane water of dialysing again;
(4), three mother liquor comprehensive utilizations:
The guanosine clear liquid of ultrafiltration membrance filter is after the elaboration crystallizer stirs decrease temperature crystalline; Three mother liquor volumes that obtain when separating with plate-and-frame filter press are big; Pigment, impurity are considerably less, and guanosine content 0.4g/L-0.5g/L can be respectively dissolves brilliant water and microfiltration membrane, the ultra-filtration membrane water of dialysing and utilize as dissolving brilliant jar.
CN2009100427858A 2009-03-04 2009-03-04 Synthetic circulation production process for guanine nucleoside Expired - Fee Related CN101492484B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009100427858A CN101492484B (en) 2009-03-04 2009-03-04 Synthetic circulation production process for guanine nucleoside

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009100427858A CN101492484B (en) 2009-03-04 2009-03-04 Synthetic circulation production process for guanine nucleoside

Publications (2)

Publication Number Publication Date
CN101492484A CN101492484A (en) 2009-07-29
CN101492484B true CN101492484B (en) 2012-02-29

Family

ID=40923291

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009100427858A Expired - Fee Related CN101492484B (en) 2009-03-04 2009-03-04 Synthetic circulation production process for guanine nucleoside

Country Status (1)

Country Link
CN (1) CN101492484B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102578389A (en) * 2012-02-15 2012-07-18 武汉工程大学 Method for producing high-protein feed by using guanosine fermentation waste liquor
CN102924551B (en) * 2012-11-30 2016-02-24 通辽梅花生物科技有限公司 A kind of method extracting guanosine from fermented liquid
CN103012528B (en) * 2013-01-22 2015-08-12 通辽梅花生物科技有限公司 A kind of method extracting guanosine from guanosine fermented liquid
CN108822163B (en) * 2018-07-13 2021-05-18 山东阳成生物科技有限公司 Comprehensive cyclic production method of D-glucosamine hydrochloride
CN112592946A (en) * 2020-12-31 2021-04-02 河南巨龙生物工程股份有限公司 Environment-friendly high-yield guanosine production process method
CN113321691B (en) * 2021-06-11 2023-04-07 肇东星湖生物科技有限公司 Guanosine purification method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1270631A (en) * 1997-07-18 2000-10-18 味之素株式会社 Process for producing purine nucleosides via fermentation
WO2008084629A1 (en) * 2006-12-22 2008-07-17 Ajinomoto Co., Inc. A method for producing purine nucleosides and nucleotides by fermentation using a bacterium belonging to the genus escherichia or bacillus

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1270631A (en) * 1997-07-18 2000-10-18 味之素株式会社 Process for producing purine nucleosides via fermentation
WO2008084629A1 (en) * 2006-12-22 2008-07-17 Ajinomoto Co., Inc. A method for producing purine nucleosides and nucleotides by fermentation using a bacterium belonging to the genus escherichia or bacillus

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
刘辉.鸟苷工程菌的构建及其发酵条件的初步研究.《中国优秀博硕士学位论文全文数据库 (硕士) 工程科技Ⅰ辑》.2007,第2007卷(第4期),第B018-19页. *
汤生荣等.发酵法生产鸟苷的生产性试验.《工业微生物》.1998,第28卷(第4期),第11-16页. *

Also Published As

Publication number Publication date
CN101492484A (en) 2009-07-29

Similar Documents

Publication Publication Date Title
CN101293847B (en) Method for extracting threonine with threonine fermentation liquor
CN101914054B (en) Comprehensive method for extracting L-tryptophan from fermentation liquor
CN101492484B (en) Synthetic circulation production process for guanine nucleoside
CN105439105B (en) The integrated processing recovery process of spent acid film and device in a kind of production process of titanium pigment
CN103979730B (en) Purify penicillin production waste liquid and the method for reclaim(ed) sulfuric acid sodium
CN102732589B (en) Method for treating threonine mother liquor
CN101863822B (en) Production method for extracting tryptophan from fermentation liquor by one-step refining
CN102659855B (en) Energy-saving environment-friendly sucrose production process
CN106186002A (en) A kind of preparation method of battery-level lithium carbonate
CN101491287A (en) Method for extracting lactose and lactoalbumin from whey and producing formulation milk powder
CN106191328A (en) A kind of xylose production process
CN101182079B (en) Citric acid mother liquor treatment process
CN101120766B (en) Monosodium glutamate green manufacturing technology
CN102745836A (en) Processing method of orange-can production wastewater
CN102584571A (en) Extraction process for shikimic acid in fermentation liquor
CN109824065A (en) A kind of method of separating magnesium and lithium and enriching lithium
CN102643209A (en) Extraction method of L-glutamine
CN105063247A (en) Sugar making process for refining cane mixed juice by use of multi-stage membrane filtration technology
CN103232353A (en) Method for separating and extracting L-valine from broth with high efficiency
CN105949276A (en) Concentration and purification energy-saving treatment process for components in corn steep liquor
CN101434554B (en) Method for all-film extraction of aminoglutaric acid
CN103804172A (en) Method for improving organic acid product quality
CN103232362B (en) Process for extracting L-glutamine
CN102071152A (en) Method for recovering yeast in fermented erythritol liquor
CN101837998A (en) Method for evaporating, concentrating and crystallizing solution of aluminum chloride

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: HUNAN HANJINGRUI AMINO ACID CO., LTD.

Free format text: FORMER OWNER: HUNAN SECO CO., LTD.

Effective date: 20130509

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20130509

Address after: 415400 No. 13 Xiangyang River Street, Jinshi City, Hunan

Patentee after: Hunan Han Jing Rui amino acid Co., Ltd.

Address before: 415400 No. 12 Xiangyang River Street, Jinshi City, Hunan

Patentee before: Hunan Seco Biotechnology Co., Ltd.

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20120229

Termination date: 20170304