CN100594238C - Production process for improving suspension cell saponin content of American ginseng - Google Patents
Production process for improving suspension cell saponin content of American ginseng Download PDFInfo
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- CN100594238C CN100594238C CN200510048270A CN200510048270A CN100594238C CN 100594238 C CN100594238 C CN 100594238C CN 200510048270 A CN200510048270 A CN 200510048270A CN 200510048270 A CN200510048270 A CN 200510048270A CN 100594238 C CN100594238 C CN 100594238C
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Abstract
The secondary metabolite cultured and produced by the plant cell suspension, special the technique to improve saponin production of American ginseng suspension cell is related in this invention. During the suspension cell culture, the final concentration of D-galactose achieves 2-40g/L by adding culture medium of D-galactose as 10-40v% of the culture volume, which increases the suspension cell growth 10-20 times and the saponin production 1-2 times up to 600-800mg/L.
Description
Technical field
The present invention relates to a kind of vegetable cell suspension culture and produce the technology of secondary metabolite, particularly improve the production technique of suspension cell saponin content of American ginseng.
Background technology
China is as the source region of herbal medicine, though natural resources of Chinese medicinal materials is abundant, standing stock are limited.Because destruction, unplanned felling and the cultivation technique etc. of ecotope are former thereby cause the rare and endangered medicinal plant kind constantly to increase.As the later stage eighties, the Radix Glycyrrhizae resource reduces 60% than the fifties, and the Moschus resource reduces 70% this fifties, and other destruction as resources such as the bark of official magnolia, the bark of eucommia, golden cypress, Chinese ephedra, Herba Cistanches, loose shellfishes is also very serious.So imbalance between supply and demand increasingly sharpens.
In plant tissue culture research, find to contain in the culturing cell medicinal ingredients such as various special meta-bolitess such as alkaloid, pigment, steroidal, terpene and essence etc., wherein some is a microorganism and manually can not synthetic, some then is just very deficient in the very little or resource of whole strain plant content own, and content is very high sometimes in cultured cells.Therefore, utilize plant cell culture technology production desirable metabolites, become the microbial technique important development field of contemporary biotechnology later on that continues.
Radix Panacis Quinquefolii (Panax quinquefolium) is a kind of rare traditional Chinese medicine of Araliaceae Panax, its contained Radix Panacis Quinquefolii Saponin is main pharmacology composition, have be good for the stomach, the effect of cardiac stimulant, calm, hypoglycemic and reducing blood-fat, and certain anti-cancer and antidotal effect are arranged.Radix Panacis Quinquefolii, the suitableeest broad-leaf forest area, mountain region that grows in about 1000 meters of height above sea level.Happiness is cloudy, and suitable skew ray and scattered light are avoided high light; Be afraid of high temperature, vegetative period, optimal temperature was 18 ℃～24 ℃; The requirement cultivating soil layer is deep, and soil property is the loam or the sandy loam of the slant acidity loose, fertile, that humus content abundant, water-permeable is strong.No matter wild the or Radix Panacis Quinquefolii of cultivation, because the physiological property of himself, poor growth generally needs four to six years ability results to be used as medicine.Their market 1 imbalance between supply and demand is outstanding, costs an arm and a leg about 1000 yuan/kg.Its saponin component still can not synthetic up to now.Therefore, by cell culture processes mass production Radix Panacis Quinquefolii Saponin, become the research focus.The Zheng Guangzhi of China, Fang Qimin, Zhou Ligang, former dawn, brave, Zhang Meiping etc. studied the culture condition of Radix Panacis Quinquefolii cell suspension culture respectively, and measured content of effective in the different culture condition low suspension cultures, for the further research of Radix Panacis Quinquefolii cell cultures provides the foundation.
At present, Radix Panacis Quinquefolii cell suspension culture technology still has the imperfection part, lack the high yield that is fit to extensive suspension culture, stable cell strain, cell suspension culture technology imperfection, suspension cell culture level and saponin output are lower, make to utilize suspended cell culture technic large-scale industrial production Radix Panacis Quinquefolii Saponin to be restricted.
Summary of the invention
Technical problem to be solved by this invention provides a kind of production technique that improves suspension cell saponin content of American ginseng, when not reducing American ginseng suspending cell yield, increase the purpose of effective desired substance content and reduction industrial production cost greatly to be implemented in.
The present invention adopts following technical scheme:
Add the nutrient solution that contains the D-semi-lactosi in the suspension cell culture process, magnitude of recruitment is the 10%-40% of volume of culture, makes D-semi-lactosi final concentration reach 2-40g/L.
The concrete implementation step of the present invention is as follows:
(1) preparation storing solution;
(2) bottling: in the storing solution that has prepared, add deionized water dilution 18-22 doubly, add white sugar, lactoalbumin hydrolysate, 2 more successively, 4-dichlorphenoxyacetic acid, α-Nai Yisuan, kinetin and indolebutyric acid, final concentration is respectively 1.5%-6%, 0.3%-1%, 0.5-1.5mg/L, 0-0.5mg/L, 0.2-1.0mg/L and 0.2-1.0mg/L, regulates the pH value then and is 5.5-6.5, fully stirs the back bottling, 100ml-500ml triangular flask, liquid amount are triangular flask volumetrical 1/5-1/2.
(3) sterilization: the sealing bottleneck, temperature is controlled at 115-122 ℃, pressure-controlling is at 1.0-1.2kg/cm
2, to sterilize 20-30 minute, the cooling back is standby.
(4) inoculation, cultivation: in the nutrient solution of making, under aseptic condition, insert the suspension cell of Radix Panacis Quinquefolii logarithmic phase, every liter of nutrient solution inserts the suspension cell of 15-50 gram fresh weight, put into the dark cultivation of shaking table suspension, replenish the nutrient solution that contains the D-semi-lactosi in culturing process, magnitude of recruitment is the 10%-40% of volume of culture, make D-semi-lactosi final concentration reach 2-40g/L, cultivated 25-35 days, harvested cell extracts the Radix Panacis Quinquefolii ginsenoside.
Technology inoculation of the present invention back culture temperature is controlled at 22-26 ℃ of dark the cultivation.
Technology shaking speed of the present invention is 90-150rpm.
Positively effect of the present invention is as follows: utilize technology of the present invention to carry out American ginseng suspending cell and cultivate, after cultivation finishes, can make cell yield increase nearly 10-20 doubly than inoculum size.The increment of cell (fresh weight) can reach about 400-600g/L, and Radix Panacis Quinquefolii ginsenoside yield increased improves 1-2 doubly, reaches 600-800mg/L.
Embodiment
Embodiment 1:
Preparation 1000ml suspension cell liquid nutrient medium, pH6.0,33 100ml triangular flasks of packing, every bottle of 30ml; Autoclaving, pressure-controlling is at 1.0kg/cm
2, 120 ℃, 20min.The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, and inoculum size is the suspension cell that every liter of nutrient solution inserts 15 gram fresh weights, 22 ℃ of culture temperature, shaking speed 90rpm, the dark cultivation.Cultivated 15 days, every bottle is replenished the nutrient solution 7.8ml that contains the D-semi-lactosi, makes the D-galactose concentration reach 15g/L, cultivates harvested cell again 10 days.Average every bottle of results fresh cell 26.2g, the Radix Panacis Quinquefolii content of ginsenoside reaches 610mg/L.
Embodiment 2:
Preparation 1000ml suspension cell liquid nutrient medium, pH5.5,33 100ml triangular flasks of packing, every bottle of 30ml; Autoclaving, pressure-controlling is at 1.2kg/cm
2, 115 ℃, 30min.The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, and inoculum size is the suspension cell that every liter of nutrient solution inserts 50 gram fresh weights, 26 ℃ of culture temperature, shaking speed 150rpm, the dark cultivation.Cultivated 25 days, every bottle is replenished the nutrient solution 12ml that contains the D-semi-lactosi, makes the D-galactose concentration reach 40g/L, cultivates harvested cell again 5 days.Average every bottle of results fresh cell 18.8g, total panaquilon content reaches 670mg/L.
Embodiment 3:
Preparation 1000ml suspension cell liquid nutrient medium, pH6.5,33 100ml triangular flasks of packing, every bottle of 30ml; Autoclaving, pressure-controlling is at 1.1kg/cm
2, 122 ℃, 25min.The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, and inoculum size is the suspension cell that every liter of nutrient solution inserts 30 gram fresh weights, 24 ℃ of culture temperature, shaking speed 120rpm, the dark cultivation.Cultivated 20 days, every bottle is replenished the nutrient solution 10ml that contains the D-semi-lactosi, makes the D-galactose concentration reach 36g/L, cultivates harvested cell again 7 days.Average every bottle of results fresh cell 23.8g, total panaquilon content reaches 630mg/L.
Claims (3)
1, a kind of production technique that improves suspension cell saponin content of American ginseng is characterized in that preparing 1000ml suspension cell liquid nutrient medium, pH6.0,33 100ml triangular flasks of packing, every bottle of 30ml; Autoclaving, pressure-controlling is at 1.0kg/cm
2, 120 ℃, 20min; The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, inoculum size is the suspension cell that every liter of nutrient solution inserts 15 gram fresh weights, 22 ℃ of culture temperature, shaking speed 90rpm, the dark cultivation cultivated 15 days, every bottle is replenished the nutrient solution 7.8ml that contains the D-semi-lactosi, make the D-galactose concentration reach 15g/L, cultivated harvested cell again 10 days; Average every bottle of results fresh cell 26.2g, Radix Panacis Quinquefolii Saponin content reaches 610mg/L.
2, a kind of production technique that improves suspension cell saponin content of American ginseng is characterized in that preparing 1000ml suspension cell liquid nutrient medium, pH5.5,33 100ml triangular flasks of packing, every bottle of 30ml; Autoclaving, pressure-controlling is at 1.2kg/cm
2, 115 ℃, 30min; The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, inoculum size is the suspension cell that every liter of nutrient solution inserts 50 gram fresh weights, 26 ℃ of culture temperature, shaking speed 150rpm, the dark cultivation cultivated 25 days, every bottle is replenished the nutrient solution 12ml that contains the D-semi-lactosi, make the D-galactose concentration reach 40g/L, cultivated harvested cell again 5 days; Average every bottle of results fresh cell 18.8g, total panaquilon content reaches 670mg/L.
3, a kind of production technique that improves suspension cell saponin content of American ginseng is characterized in that preparing 1000ml suspension cell liquid nutrient medium, pH6.5,33 100ml triangular flasks of packing, every bottle of 30m l; Autoclaving, pressure-controlling is at 1.1kg/cm
2, 122 ℃, 25min; The American ginseng suspending cell of taking the logarithm vegetative period is inoculated in the 100mL triangular flask, inoculum size is the suspension cell that every liter of nutrient solution inserts 30 gram fresh weights, 24 ℃ of culture temperature, shaking speed 120rpm, the dark cultivation cultivated 20 days, every bottle is replenished the nutrient solution 10ml that contains the D-semi-lactosi, make the D-galactose concentration reach 36g/L, cultivated harvested cell again 7 days; Average every bottle of results fresh cell 23.8g, total panaquilon content reaches 630mg/L.
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| CN200510048270A CN100594238C (en) | 2005-12-31 | 2005-12-31 | Production process for improving suspension cell saponin content of American ginseng |
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| CN200510048270A CN100594238C (en) | 2005-12-31 | 2005-12-31 | Production process for improving suspension cell saponin content of American ginseng |
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| CN100594238C true CN100594238C (en) | 2010-03-17 |
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Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104737916B (en) * | 2015-04-17 | 2017-05-03 | 安徽农业大学 | Suspension culture method for producing quiquefolium saponins |
| CN104920209A (en) * | 2015-05-18 | 2015-09-23 | 天津大学 | Method for taking two inducers to promote ginseng adventitious saponin accumulation |
| CN104871973A (en) * | 2015-05-18 | 2015-09-02 | 天津大学 | Method for accelerating accumulation of saponin in ginseng adventitious roots by adopting two types of inductors |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1135528A (en) * | 1994-12-21 | 1996-11-13 | 广州市天河区嘉兰德生物工程有限公司 | Simple industrial production method of fresh American ginseng cells |
| CN1149587A (en) * | 1995-10-30 | 1997-05-14 | 中国科学院昆明植物研究所 | Ginseng oligosaccharide element and ginseng monomer oligosaccharide and its preparing technology and use |
| US6326202B1 (en) * | 1999-10-19 | 2001-12-04 | Council Of Scientific & Industrial Research | Stable high ginsenoside-yielding callus line of Panax quinquefolium (American ginseng) and a method for developing such stable high ginsenoside-yielding callus line |
-
2005
- 2005-12-31 CN CN200510048270A patent/CN100594238C/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1135528A (en) * | 1994-12-21 | 1996-11-13 | 广州市天河区嘉兰德生物工程有限公司 | Simple industrial production method of fresh American ginseng cells |
| CN1149587A (en) * | 1995-10-30 | 1997-05-14 | 中国科学院昆明植物研究所 | Ginseng oligosaccharide element and ginseng monomer oligosaccharide and its preparing technology and use |
| US6326202B1 (en) * | 1999-10-19 | 2001-12-04 | Council Of Scientific & Industrial Research | Stable high ginsenoside-yielding callus line of Panax quinquefolium (American ginseng) and a method for developing such stable high ginsenoside-yielding callus line |
Non-Patent Citations (4)
| Title |
|---|
| Saponin production in callus and cell suspension cultures ofPANAX QUINQUEFOLIUM. Archana Mathur, et al..Phytochemistry,Vol.35 No.5. 1994 * |
| SaponinproductionincallusandcellsuspensionculturesofPANAXQUINQUEFOLIUM.ArchanaMathur et al..Phytochemistry |
| 西洋参悬浮细胞培养条件的研究. 原晓勇等.西北大学学报（自然科学版），第24卷第1期. 1994 |
| 西洋参悬浮细胞培养条件的研究. 原晓勇等.西北大学学报(自然科学版)，第24卷第1期. 1994 * |
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Application publication date: 20060719 Assignee: The Huanshui River, Shijiazhuang all living creatures' thing Science and Technology Ltd. Assignor: Hebei Biology Institute Contract record no.: 2012130000166 Denomination of invention: Production process for improving suspension cell saponin content of American ginseng Granted publication date: 20100317 License type: Exclusive License Record date: 20120914 |
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