CN104663441A - Large-scale manufacture method of high-precision BL (containing mounting medium) culture substance - Google Patents

Large-scale manufacture method of high-precision BL (containing mounting medium) culture substance Download PDF

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Publication number
CN104663441A
CN104663441A CN201510082514.0A CN201510082514A CN104663441A CN 104663441 A CN104663441 A CN 104663441A CN 201510082514 A CN201510082514 A CN 201510082514A CN 104663441 A CN104663441 A CN 104663441A
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matrix
mother liquor
precision
cocl2
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钱家静
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    • Y02P60/216

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  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

The invention discloses a large-scale manufacture method of a high-precision BL (containing mounting medium) culture substance and belongs to the technical field of plant biology. The method comprises the following steps: firstly calculating the quantity demand of 18 elements of the substance, after being amplified for 1000 times, and the quantity demands of the CuSO4*5H2O and the CoCl2*6H2O, after being amplified for 10000 times; accurately weighing the medicines; mixing and sealing the 18 elements in turn according to the quantity demands from less to more; dissolving the 10000 times of CuSO4*5H2O and CoCl2*6H2O with 1L of distilling water for later use; respectively unsealing according to demand. By adopting the method, the amplified substance has the characteristics of being high in precision, convenient and rapid in operation, simple in application and small in error in different batches and in the same batch, the phenomenon of big error, sediment and mildew caused by the manual operation and the external factor influence can be avoided and the method can be applied to the biotechnology such as plant tissue culture.

Description

A kind of scale preparation method of high accuracy BL (containing mounting medium) culture matrix
Technical field
The invention discloses the scale preparation method of a kind of high accuracy BL (containing mounting medium) culture matrix, belong to plant biotechnology field.Be more particularly one include accurate calculating, accurate weighing, first few after how mix, seal, mother liquor preparation separately, six steps such as use of breaking seal, to acquisition different batches and batch between the minimum culture matrix of error, minimizing experimental error method.
Background technology
Plant tissue culture technique or cultivation technique without soil need preparation medium mother liquor usually, and namely preparation expands certain multiple, liquid containing all kinds reagent.But, because mother liquor contains dissimilar reagent, be usually divided into the large class of macroelement, trace element, molysite and organic element four, and the multiple that four large classes expand is different, causes medicine service property (quality) inconsistent, easily occurs the error of calculation first; Second the producer of medicine, quality are inconsistent, even if to calculate, weigh consistent, also can affect result of the test; Three due to mother liquor be liquid condition, at the end of spring and the beginning of summer season, because the temperature rises and humidity increases, extremely easily cause mother liquor bacterial infection, mould, cause the phenomenon presenting different colours in mother liquor or occur precipitation, waste raw material; Comparatively big error can be there is to the difference of the cognition of container scale (especially trace element), instrument precision in four fundamental rules because of weighing person.
In view of the above-mentioned shortcoming of mother liquor; with the mother liquor medium of routine; usually there will be the failed phenomenon that maybe cannot repeat of the result of the test caused because of factors such as weighing person, medicine, seasons; have impact on the process using Plant Tissue Breeding or cultivation technique without soil to carry out test greatly, hit the confidence of experimenter.
Summary of the invention
A kind of scale preparation method of high accuracy BL (containing mounting medium) culture matrix; it is characterized in that, include in described method accurate calculating, accurate weighing, first few after how mix, seal, prepared by independent mother liquor, six steps such as use of breaking seal.
Method according to claim 1, is characterized in that, six described step concrete operations are as follows:
1. accurately calculate: 17 kinds of elements contained by BL minimal medium are expanded 1000 times, i.e. Sodium Molybdate Dihydrate 0.25g, nicotinic acid 0.5g, potassium iodide 0.83g, boric acid 6.2g, white vitriol 10.6g, four water manganese sulphate 22.3g, iron edetate 36.5g, inositol 100g, aspartoyl 100g, potassium dihydrogen phosphate 170g, epsom salt 370g, calcium chloride dihydrate 440g, ammonium nitrate 1650g, potassium nitrate 1900g, agar powder 5000g; 2 kinds of element CoCL2 6H2Os and cupric sulfate pentahydrate expand 10000 times, i.e. each 0.25g;
2. accurate weighing: according to the result precise of 1. middle calculating, especially with CoCL2 6H2O and the cupric sulfate pentahydrate of each 0.25g of ten thousand/balance precise;
3. how to mix after first few: mix according to few priority of carrying out of amount more, namely according to Sodium Molybdate Dihydrate, nicotinic acid, potassium iodide, boric acid, white vitriol, four water manganese sulphates, iron edetate, inositol, aspartoyl, potassium dihydrogen phosphate, epsom salt, calcium chloride dihydrate, ammonium nitrate, potassium nitrate, the order of agar powder mixes, and amounts to 9707.73g;
4. seal: the requirement of mixed solid matrix according to 250g every bottle is sub-packed in plastic containers, and seals;
5. mother liquor preparation separately: CoCL2 6H2O and cupric sulfate pentahydrate respectively weigh 0.25g, are dissolved in 1L distilled water, are mixed with 10000 times of mother liquors;
6. to break seal use: as required, add the above-mentioned solid matrix 9.7g of precise in every 1L distilled water, heating adds the independent mother liquor of 100 μ L CoCL2 6H2Os and cupric sulfate pentahydrate after it dissolves completely, and then adds reagent needed for other.
Beneficial effect of the present invention: the scale preparation method of this high precision culture matrix has following characteristics, i.e. without the error of calculation between the matrix of different batches; Because 17 kinds of reagent all expand 1000 times, 2 kinds of reagent expand 10000 times, and the weighing error between the matrix of different batches is minimum, and precision is high; In theory, due to the usage amount (calculating with each 1L) that solid matrix is 1000 times at every turn, namely the above-mentioned formula of 1000L can be prepared, liquid mother liquor only needs 100 μ L at every turn, and batch inside there will not be the human error caused because using the reagent of different manufacturers, different times; Solid matrix after expansion is that every 250g is sealed in plastic containers, can avoid because the impact of the extraneous factor such as weather, temperature, moisture causes occurring the common precipitation of liquid mother liquor, the phenomenon such as mouldy, and fluid matrix is only the mixing of two kinds of elements.After expanding 10000 times, precision is high; Above-mentioned plurality of advantages is all the follow-up test carried out for matrix with this medium, obtains result of the test accurately and lays the foundation.。
Embodiment:
Below in conjunction with specific embodiment, the present invention is conducted further description.
The scale preparation method of a kind of high accuracy BL (containing mounting medium) (carbonaceous sources and mounting medium) solid culture matrix in the present embodiment, include accurate calculating, accurate weighing, first few after how mix, seal, prepared by independent mother liquor, six steps such as use of breaking seal.
Above-mentioned six step concrete operations are as follows:
1. accurately calculate: 17 kinds of elements contained by BL minimal medium are expanded 1000 times, i.e. Sodium Molybdate Dihydrate 0.25g, nicotinic acid 0.5g, potassium iodide 0.83g, boric acid 6.2g, white vitriol 10.6g, four water manganese sulphate 22.3g, iron edetate 36.5g, inositol 100g, aspartoyl 100g, potassium dihydrogen phosphate 170g, epsom salt 370g, calcium chloride dihydrate 440g, ammonium nitrate 1650g, potassium nitrate 1900g, agar powder 5000g; 2 kinds of element CoCL2 6H2Os and cupric sulfate pentahydrate expand 10000 times, i.e. each 0.25g;
2. accurate weighing: according to the result precise of 1. middle calculating, especially with CoCL2 6H2O and the cupric sulfate pentahydrate of each 0.25g of ten thousand/balance precise;
3. how to mix after first few: mix according to few priority of carrying out of amount more, namely according to Sodium Molybdate Dihydrate, nicotinic acid, potassium iodide, boric acid, white vitriol, four water manganese sulphates, iron edetate, inositol, aspartoyl, potassium dihydrogen phosphate, epsom salt, calcium chloride dihydrate, ammonium nitrate, potassium nitrate, the order of agar powder mixes, and amounts to 9707.73g;
4. seal: the requirement of mixed solid matrix according to 250g every bottle is sub-packed in plastic containers, and seals;
5. mother liquor preparation separately: CoCL2 6H2O and cupric sulfate pentahydrate respectively weigh 0.25g, are dissolved in 1L distilled water, are mixed with 10000 times of mother liquors;
6. to break seal use: as required, add the above-mentioned solid matrix 9.7g of precise in every 1L distilled water, heating adds the independent mother liquor of 100 μ L CoCL2 6H2Os and cupric sulfate pentahydrate after it dissolves completely, and then adds reagent needed for other.
1L solution after above-mentioned substrate preparation is added the sucrose of 30g, and then add the KOH of 1N of 1ml, dissolve completely and be sub-packed in the vial of 30 200ml, after 121 DEG C of sterilizing 20min.On superclean bench, inoculate stevia stem section, after cultivating 28d under 25 DEG C of illumination 12h conditions, occur axillalry bud and take root good.

Claims (3)

1. the scale preparation method of high accuracy BL (containing a mounting medium) culture matrix; it is characterized in that, include in described method accurate calculating, accurate weighing, first few after how mix, seal, prepared by independent mother liquor, six steps such as use of breaking seal.
2. method according to claim 1, is characterized in that, six described step concrete operations are as follows:
1. accurately calculate: 17 kinds of elements contained by BL minimal medium are expanded 1000 times, i.e. Sodium Molybdate Dihydrate 0.25g, nicotinic acid 0.5g, potassium iodide 0.83g, boric acid 6.2g, white vitriol 10.6g, four water manganese sulphate 22.3g, iron edetate 36.5g, inositol 100g, aspartoyl 100g, potassium dihydrogen phosphate 170g, epsom salt 370g, calcium chloride dihydrate 440g, ammonium nitrate 1650g, potassium nitrate 1900g, agar powder 5000g; 2 kinds of element CoCL2 6H2Os and cupric sulfate pentahydrate expand 10000 times, i.e. each 0.25g;
2. accurate weighing: according to the result precise of 1. middle calculating, especially with CoCL2 6H2O and the cupric sulfate pentahydrate of each 0.25g of ten thousand/balance precise;
3. how to mix after first few: mix according to few priority of carrying out of amount more, namely according to Sodium Molybdate Dihydrate, nicotinic acid, potassium iodide, boric acid, white vitriol, four water manganese sulphates, iron edetate, inositol, aspartoyl, potassium dihydrogen phosphate, epsom salt, calcium chloride dihydrate, ammonium nitrate, potassium nitrate, the order of agar powder mixes, and amounts to 9707.73g;
4. seal: the requirement of mixed solid matrix according to 250g every bottle is sub-packed in plastic containers, and seals;
5. mother liquor preparation separately: CoCL2 6H2O and cupric sulfate pentahydrate respectively weigh 0.25g, are dissolved in 1L distilled water, are mixed with 10000 times of mother liquors;
6. to break seal use: as required, add the above-mentioned solid matrix 9.7g of precise in every 1L distilled water, heating adds the independent mother liquor of 100 μ L CoCL2 6H2Os and cupric sulfate pentahydrate after it dissolves completely, and then adds reagent needed for other.
3. method according to claim 1, is characterized in that, the scale preparation method of this high precision culture matrix has following characteristics, i.e. without the error of calculation between the matrix of different batches; Because 17 kinds of reagent all expand 1000 times, 2 kinds of reagent expand 10000 times, and the weighing error between the matrix of different batches is minimum, and precision is high; In theory, due to the usage amount (calculating with each 1L) that solid matrix is 1000 times at every turn, namely the above-mentioned formula of 1000L can be prepared, liquid mother liquor only needs 100 μ L at every turn, and batch inside there will not be the human error caused because using the reagent of different manufacturers, different times; Solid matrix after expansion is that every 250g is sealed in plastic containers, can avoid because the impact of the extraneous factor such as weather, temperature, moisture causes occurring the common precipitation of liquid mother liquor, the phenomenon such as mouldy, and fluid matrix is only the mixing of two kinds of elements; After expanding 10000 times, precision is high; Above-mentioned plurality of advantages is all the follow-up test carried out for matrix with this medium, obtains result of the test accurately and lays the foundation.
CN201510082514.0A 2015-02-16 2015-02-16 Large-scale manufacture method of high-precision BL (containing mounting medium) culture substance Pending CN104663441A (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006254832A (en) * 2005-03-18 2006-09-28 Sanei Gen Ffi Inc Solid medium
CN101070531A (en) * 2006-05-09 2007-11-14 陈曦 Dry-powder-type culturing substrate and preparing method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006254832A (en) * 2005-03-18 2006-09-28 Sanei Gen Ffi Inc Solid medium
CN101070531A (en) * 2006-05-09 2007-11-14 陈曦 Dry-powder-type culturing substrate and preparing method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
仪宏等: "脱水植物组织培养基的制备", 《河北轻化工学院学报》 *

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Application publication date: 20150603