CN1687138A - Method for preparing grape manna oligosaccharide - Google Patents
Method for preparing grape manna oligosaccharide Download PDFInfo
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- CN1687138A CN1687138A CN 200510034300 CN200510034300A CN1687138A CN 1687138 A CN1687138 A CN 1687138A CN 200510034300 CN200510034300 CN 200510034300 CN 200510034300 A CN200510034300 A CN 200510034300A CN 1687138 A CN1687138 A CN 1687138A
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- grape
- enzyme
- preparation
- manna
- manna oligosaccharide
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Abstract
The present invention relates to a preparation method of glucomannan oligosaccharide. It is characterized by that the glucomannan oligosaccharide can be obtained by dissolving 2 mass% of konjak fine flour in 1 mass% of glucomannan oligosaccharidase liquor through the process of water-bath enzymolysis, in which the glucomannan oligosaccharidase is obtained by using strain of Trichoderma viride CGMCC3.2942 and adopting the steps of culture in slant culture medium containing konjak fine flour, inoculating yeast culture and enzyme liquor extraction, etc.
Description
Technical field
The present invention relates to a kind of preparation method of grape manna oligosaccharide, relate in particular to a kind of method for preparing grape manna oligosaccharide by homemade mannan oligosaccharide enzymic hydrolysis konjaku powder.
Background technology
The restriction of factors such as the many cell wallss with microorganism (mainly being yeast) of method that prepare grape manna oligosaccharide both at home and abroad at present are extracted as the master, therefore are subjected to the starting material source deficient, and extracting method complexity and yield are low, the application of grape manna oligosaccharide is affected.Thus, searching source approach abundant, that preparation technology is simple, yield is high prepares grape manna oligosaccharide has just had significant meaning.
Summary of the invention
The object of the present invention is to provide a kind of starting material source abundant, preparation technology is simple, the preparation method of dear money, highly active grape manna oligosaccharide.
The present invention is a raw material with resourceful konjaku powder, by specific homemade grape manna oligosaccharide enzyme, and with the simple technology of gentleness, preparation high purity, highly active grape manna oligosaccharide, thus realized purpose of the present invention.
The preparation method of grape manna oligosaccharide of the present invention is characterized in that may further comprise the steps:
(1) spawn culture: wherein bacterial classification is viride (Trichoderma viride) CGMCC3.2942, and substratum is in mass fraction, by 6 parts of bagasses, and 2 parts in wheat bran, 0.5 part of konjaku powder, (NH
4)
2SO
42 parts, KH
2PO
41 part, MgSO
40.05 part, 1.5 parts in agar, 100 parts of compositions of water; Method with routine prepares slant medium cultivation bacterial classification, obtains the inclined-plane kind;
(2) bacterium is bent cultivates: the inclined-plane kind is made spore suspension with ordinary method, and the bottle that spore suspension is put into substratum carried out 4 days bent cultivations of bacterium under 28 ℃, described substratum is that 1: 2.2 solid medium and nutrition salt solution is formed by mass ratio, wherein solid medium is in massfraction, by bagasse 70%, wheat bran 27%, konjaku powder 3% is formed, nutrition salt solution is in massfraction, by (NH
4)
2SO
40.5%, KH
2PO
40.05%, MgSO
40.025% and water 99.425% form;
(3) enzyme liquid extracting: cultured bacterium song adds 32 ℃ of distilled water, 30 ℃ of extracting at constant temperature, and filter cleaner, the filtrate centrifugation, supernatant liquor is a grape manna oligosaccharide enzyme crude enzyme liquid;
(4) konjaku powder enzymolysis: it is 1% enzyme liquid that grape manna oligosaccharide enzyme liquid is made into by pure enzyme massfraction with distilled water, the adding massfraction is 2% konjaku powder in the stirring, the rearmounted 40 ℃ of water enzyme digestion 2h of dissolving, after enzymolysis finishes, keep 20min under 80 ℃ and go out that enzyme is lived and cooling, the liquid grape manna oligosaccharide.
The used culture presevation of the present invention is in China Committee for Culture Collection of Microorganisms, and preserving number is CGMCC3.2942.
The preferred version and the condition of abovementioned technology are as follows: the preparation of the described substratum of step 1 is earlier that agar is molten with poach, again with konjaku powder, and (NH
4)
2SO
4, KH
2PO
4And MgSO
4Dissolving adds bagasse, the abundant mixing of wheat bran while hot;
The preparation method of the described substratum of step 2 adds swelling in the nutrition salt solution with konjaku powder earlier, again with bagasse and the abundant mixing of wheat bran;
The extracting at constant temperature time of step 3 is 2h, and filtrate centrifugation time under the rotating speed of 5000r/min is 15min; Described crude enzyme liquid preferably is purified to solid enzyme powder, method is to add pre-cooled ethanol under ice bath while stirring lentamente, make alcohol concn reach 65%, leave standstill under 4 ℃, preferably leave standstill 3h, abandon supernatant liquid, be deposited under the rotating speed of 5000r/min centrifugal, best centrifugal 20min, get thick enzyme mud, thick enzyme mud dissolves with the lyase elutriant, and the mass ratio of enzyme mud and elutriant is 1: 8 in the lyase elutriant, wherein elutriant pH=5.4 is dissolved in the 1000mL water and is made by saltpetre, calcium chloride, each 2mg of Trisodium Citrate; The centrifugal purification under the rotating speed of 5000r/min of enzyme liquid after the dissolving, best centrifugal 20min gets pure enzyme liquid.
The liquid grape manna oligosaccharide that the present invention obtains concentrates the spray-dried powdery grape manna oligosaccharide that obtains of concentrated solution through ultrafiltration or vacuum decompression.
The present invention adopts pure biological preparation, and preparation technology is simple, safety, and cost is low, the grape manna oligosaccharide biological activity height that obtains.
Embodiment
Following embodiment further specifies of the present invention, but the invention is not restricted to following embodiment.
Embodiment 1:
1.5g agar is molten with the 100mL poach, and with konjaku powder 0.5g, (NH
4)
2SO
42g, KH
2PO
41g, MgSO
40.05g dissolving, add bagasse 6g, wheat bran 2g and abundant mixing while hot, substratum is spread out cooling, be cut into strip, pack in right amount in the test tube, 0.11MPa sterilization 30min puts into the inclined-plane, inserts viride (Trichoderma viride) CGMCC3.2942, obtain one of inclined-plane kind, and make spore suspension 100mL.
(NH
4)
2SO
41.1g, KH
2PO
40.11g, MgSO
40.055g add in the 218.735g distilled water and make 220g nutrition salt solution.Konjaku powder 3g is added swelling in the nutrition salt solution, and again with bagasse 70g, the abundant mixing of wheat bran 27g, the substratum that obtains are sub-packed in the 1000mL triangular flask, every bottled substratum 100g, the 0.11MPa 30min that sterilizes.Every then triangular flask inserts spore suspension 8mL, shakes up back 28 ℃ and cultivates 4 days, obtains the bacterium song.
The bent every triangular flask of cultured bacterium adds 32 ℃ of distilled water 150mL, 30 ℃ of extracting at constant temperature 2h, and filter cleaner, the centrifugal 15min of filtrate 5000r/min, supernatant liquor are crude enzyme liquid.Enzyme liquid extracts with 95% pre-cooled ethanol precipitation.Add pre-cooled ethanol under the ice bath while stirring lentamente, make alcohol concn reach 65%, leave standstill 3h under 4 ℃, abandon supernatant, be deposited in the centrifugal 20min of 5000r/min, get thick enzyme mud, saltpetre, calcium chloride, each 2mg of Trisodium Citrate is dissolved in the lyase elutriant that is made into pH5.4 in the 1000mL water, in enzyme mud: the ratio of elutriant=1: 8 with enzyme mud with the dissolving of lyase elutriant after, the centrifugal 20min of 5000r/min purifies, the dense enzyme liquid of must purifying, and the pure grape manna oligosaccharide enzyme with 1g after the lyophilize is made into enzyme liquid with 97g distilled water, add the 2g konjaku powder in the stirring, the rearmounted 40 ℃ of water enzyme digestion 2h of dissolving after enzymolysis finishes, keep the 20min enzyme that goes out under 80 ℃ and live, cooling gets the liquid grape manna oligosaccharide.The liquid grape manna oligosaccharide concentrates through vacuum decompression, the spray-dried powdery grape manna oligosaccharide that obtains of concentrated solution.
Embodiment 2:
The liquid grape manna oligosaccharide that embodiment 1 obtains is measured through the HPLC of China Guangzhou Analysis ﹠. Test Center, examines to such an extent that the content of mannan oligosaccharide is 16.5g/L.
Claims (7)
1. the preparation method of a grape manna oligosaccharide is characterized in that may further comprise the steps:
(1) spawn culture: wherein bacterial classification is viride (Trichoderma viride) CGMCC3.2942, and substratum is in mass fraction, by 6 parts of bagasses, and 2 parts in wheat bran, 0.5 part of konjaku powder, (NH
4)
2SO
42 parts, KH
2PO
41 part, MgSO
40.05 part, 1.5 parts in agar, 100 parts of compositions of water, the preparation slant medium is cultivated bacterial classification, obtains the inclined-plane kind;
(2) bacterium is bent cultivates: the inclined-plane kind is made spore suspension, and the bottle that spore suspension is put into substratum carried out 4 days bent cultivations of bacterium under 28 ℃, described substratum is that 1: 2.2 solid medium and nutrition salt solution is formed by mass ratio, wherein solid medium is in massfraction, by bagasse 70%, wheat bran 27%, konjaku powder 3% is formed, nutrition salt solution is in massfraction, by (NH
4)
2SO
40.5%, KH
2PO
40.05%, MgSO
40.025% and water 99.425% form;
(3) enzyme liquid extracting: cultured bacterium song adds 32 ℃ of distilled water, 30 ℃ of extracting at constant temperature, and filter cleaner, the filtrate centrifugation, supernatant liquor is a grape manna oligosaccharide enzyme crude enzyme liquid;
(4) konjaku powder enzymolysis: it is 1% enzyme liquid that grape manna oligosaccharide enzyme liquid is made into by pure enzyme massfraction with distilled water, the adding massfraction is 2% konjaku powder in the stirring, the rearmounted 40 ℃ of water enzyme digestion 2h of dissolving, the enzyme that goes out live and cool off the liquid grape manna oligosaccharide.
2. the preparation method of a kind of grape manna oligosaccharide according to claim 1, the preparation that it is characterized in that the described substratum of step 1 is earlier that agar is molten with poach, again with konjaku powder, (NH
4)
2SO
4, KH
2PO
4And MgSO
4Dissolving adds bagasse, the abundant mixing of wheat bran while hot.
3. the preparation method of a kind of grape manna oligosaccharide according to claim 1, the preparation method who it is characterized in that the described substratum of step 2 add swelling in the nutrition salt solution with konjaku powder earlier, again with bagasse and the abundant mixing of wheat bran.
4. the preparation method of a kind of grape manna oligosaccharide according to claim 1 is characterized in that the extracting at constant temperature time of step 3 is 2h, and filtrate is at the centrifugal 15min of 5000r/min.
5. according to the preparation method of claim 1 or 4 described a kind of grape manna oligosaccharides, it is characterized in that described crude enzyme liquid is purified to pure enzyme liquid, its method is made up of following steps:
Under ice bath, add pre-cooled ethanol while stirring lentamente, alcohol concn is reached under 65%, 4 ℃ leave standstill 3h, abandon supernatant liquid, be deposited in the centrifugal 20min of 5000r/min, get thick enzyme mud, thick enzyme mud dissolves with the lyase elutriant, and the mass ratio of enzyme mud and elutriant is 1: 8 in the lyase elutriant, elutriant pH=5.4 wherein, be dissolved in the 1000mL water and made by saltpetre, calcium chloride, each 2mg of Trisodium Citrate, the enzyme liquid after the dissolving gets pure enzyme liquid at the centrifugal 20min of 5000r/min.
6. the preparation method of a kind of grape manna oligosaccharide according to claim 1 is characterized in that the described sterilization work of step 4 is to keep 20min under 80 ℃.
7. according to the preparation method of claim 1 or 2 or 3 or 4 or 6 described a kind of grape manna oligosaccharides, it is characterized in that the described liquid grape manna oligosaccharide of step 4 concentrates the spray-dried powdery grape manna oligosaccharide that obtains of concentrated solution through ultrafiltration or vacuum decompression.
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CN 200510034300 CN1259427C (en) | 2005-04-22 | 2005-04-22 | Method for preparing grape manna oligosaccharide |
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CN 200510034300 CN1259427C (en) | 2005-04-22 | 2005-04-22 | Method for preparing grape manna oligosaccharide |
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CN1687138A true CN1687138A (en) | 2005-10-26 |
CN1259427C CN1259427C (en) | 2006-06-14 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101182500B (en) * | 2007-11-01 | 2010-04-14 | 广东省微生物研究所 | Glucomannan enzyme preparation method |
CN112280814A (en) * | 2020-10-29 | 2021-01-29 | 武汉芘芘薇莎生物科技有限公司 | High-content medium-low molecular weight konjac glucomannan, preparation method thereof and functional composition thereof |
-
2005
- 2005-04-22 CN CN 200510034300 patent/CN1259427C/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101182500B (en) * | 2007-11-01 | 2010-04-14 | 广东省微生物研究所 | Glucomannan enzyme preparation method |
CN112280814A (en) * | 2020-10-29 | 2021-01-29 | 武汉芘芘薇莎生物科技有限公司 | High-content medium-low molecular weight konjac glucomannan, preparation method thereof and functional composition thereof |
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Publication number | Publication date |
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CN1259427C (en) | 2006-06-14 |
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Granted publication date: 20060614 Termination date: 20200422 |