JPS6319308Y2 - - Google Patents
Info
- Publication number
- JPS6319308Y2 JPS6319308Y2 JP18502883U JP18502883U JPS6319308Y2 JP S6319308 Y2 JPS6319308 Y2 JP S6319308Y2 JP 18502883 U JP18502883 U JP 18502883U JP 18502883 U JP18502883 U JP 18502883U JP S6319308 Y2 JPS6319308 Y2 JP S6319308Y2
- Authority
- JP
- Japan
- Prior art keywords
- container
- solvent
- condensation
- dna
- synthesis
- 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
Links
- 239000002904 solvent Substances 0.000 claims description 40
- 238000009833 condensation Methods 0.000 claims description 30
- 230000005494 condensation Effects 0.000 claims description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 230000006820 DNA synthesis Effects 0.000 claims description 18
- 238000010521 absorption reaction Methods 0.000 claims description 16
- 239000003153 chemical reaction reagent Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 238000003786 synthesis reaction Methods 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 9
- 230000002194 synthesizing effect Effects 0.000 claims description 4
- 239000006096 absorbing agent Substances 0.000 description 11
- 238000005406 washing Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000000873 masking effect Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002808 molecular sieve Substances 0.000 description 4
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 4
- 238000006482 condensation reaction Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 230000006819 RNA synthesis Effects 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
Description
【考案の詳細な説明】
(イ) 産業上の利用分野
この考案は、DNA合成、さらにはRNA合成を
おこなう装置に関し、とくにその縮合用溶媒の吸
水機構に関するものである。[Detailed explanation of the invention] (a) Industrial application field This invention relates to an apparatus for DNA synthesis and further RNA synthesis, and in particular relates to the water absorption mechanism of the condensation solvent.
(ロ) 従来技術
DNA合成は、マスキング、脱保護、乾燥、縮
合の各反応で構成される。このうち、DNA合成
の主反応とも言える縮合反応は水によつて著しく
阻害される。反応スケールが小さくなるぼど微量
の水が問題となる。一方遺伝子工学の必要とする
DNA量は非常に少なく、また合成用の核酸試薬
が高価なため反応スケールは、ますます小さくな
る傾向にある。現在、縮合用溶媒は、1回合成が
終るたびに新しいものと取りかえたり、モレキユ
ラ シーブを液中に、投入したりしているが、前
者は操作が繁雑であり、後者はモレキユラ シー
ブの微粒子が流路中に侵入して、電磁弁などを破
損する。(b) Prior art DNA synthesis consists of masking, deprotection, drying, and condensation reactions. Among these, the condensation reaction, which can be said to be the main reaction of DNA synthesis, is significantly inhibited by water. As the reaction scale becomes smaller, trace amounts of water become a problem. On the other hand, genetic engineering requires
Since the amount of DNA is very small and the nucleic acid reagents for synthesis are expensive, the reaction scale tends to become smaller and smaller. Currently, the condensation solvent is replaced with a new one every time one synthesis is completed, or Molecular Sieve is added to the liquid, but the former method is complicated to operate, and the latter method is difficult because the fine particles of Molecular Sieve are added to the solution. It can enter the flow path and damage solenoid valves, etc.
(ハ) 目的
この考案は上記の事情に鑑みなしたもので、溶
媒内に吸水剤が混入せず、かつ複数回の合成工程
においても縮合用溶媒を取り換える必要のない
DNA等合成装置を提供しようとするものである。(c) Purpose This invention was developed in view of the above circumstances, and it is possible to avoid mixing water absorbing agents into the solvent and eliminate the need to replace the condensation solvent even during multiple synthesis steps.
The aim is to provide a device for synthesizing DNA, etc.
(ニ) 構成
この考案においては、縮合用溶媒容器から延出
するチユーブに吸水カラムを組みこんだもので、
そのさらに詳しい構成は、複数個のDNA等合成
試薬容器と縮合剤容器と各種試薬容器と縮合用溶
媒容器と合成反応容器とを備え、合成反応容器内
においてDNA等の合成のなされるDNA等合成装
置において、縮合用溶媒容器から延出する縮合用
溶媒の引き出しチユーブに、内部のフイルター材
によつて区画される空間内に吸水剤が充填された
吸水カラムを組みこんだことを特徴とするDNA
等合成装置に示す通りである。(d) Configuration In this invention, a water absorption column is incorporated into a tube extending from a condensation solvent container.
Its more detailed configuration includes a plurality of reagent containers for DNA synthesis, a condensing agent container, various reagent containers, a condensation solvent container, and a synthesis reaction container. A DNA apparatus characterized in that a water absorption column filled with a water absorption agent is incorporated into a condensation solvent extraction tube extending from a condensation solvent container in a space defined by an internal filter material.
As shown in the iso-synthesizer.
(ホ) 実施例
以下この考案の実施例を図面により詳述する
が、この考案は以下の実施例に限定されるもので
はない。(e) Examples Examples of this invention will be described below in detail with reference to the drawings, but this invention is not limited to the following examples.
第1図はこの考案のDNA等合成装置の全体構
成を示す。 Figure 1 shows the overall configuration of this device for synthesizing DNA, etc.
1は調整用容器であり、粉末のDNA等合成試
薬と縮合剤とが収納されるDNA等合成試薬容器
2と縮合剤容器3とが垂直方向に一体に構成され
ている。4が反応の際に支持体が収納される合成
反応容器である。5はマスキング試薬容器、6,
7は洗浄、乾燥用の溶媒容器である。8が縮合用
溶媒容器で、この縮合用溶媒容器8から調整用容
器1に至る縮合用溶媒の引き出しチユーブ9に吸
水カラム10が組み込まれている。 Reference numeral 1 denotes an adjustment container, in which a DNA synthesis reagent container 2 and a condensing agent container 3, in which a powdered DNA synthesis reagent and a condensing agent are stored, and a condensing agent container 3 are vertically integrated. 4 is a synthesis reaction vessel in which a support is housed during the reaction. 5 is a masking reagent container; 6;
7 is a solvent container for washing and drying. 8 is a condensation solvent container, and a water absorption column 10 is installed in a condensation solvent extraction tube 9 extending from the condensation solvent container 8 to the adjustment container 1.
第1図は略図であり、例えば調整用容器1は実
際にはさらに多数個であり、またシリンジポンプ
や弁等の図示も省略している。 FIG. 1 is a schematic diagram; for example, there are actually many more adjustment containers 1, and illustrations of syringe pumps, valves, etc. are also omitted.
DNAの合成工程を簡略に述べると、まず洗浄
乾燥用の溶媒容器6,7からの溶媒により合成反
応容器4、さらにはその内部の支持体の洗浄およ
び乾燥をおこなう。次に縮合用溶媒容器8から溶
媒を一つの調整用容器1に至らせ、溶媒により
DNA合成試薬と縮合剤とが混合され、その溶液
が合成反応容器4に至つてDNA合成がおこなわ
れる。次にさらに洗浄、マスキング試薬によるマ
スキング、洗浄がおこなわれDNA合成に第1の
工程が終了する。そして、さらに別の調整用容器
1に縮合用溶媒容器8から合成反応容器4への流
路が切り換えられ上記と同様の合成工程がおこな
われる。 Briefly describing the DNA synthesis process, first, the synthesis reaction vessel 4 and the support therein are washed and dried using the solvent from the solvent vessels 6 and 7 for washing and drying. Next, the solvent is brought from the condensation solvent container 8 to one adjustment container 1, and the solvent
A DNA synthesis reagent and a condensing agent are mixed, and the resulting solution reaches the synthesis reaction vessel 4, where DNA synthesis is performed. Next, further washing, masking with a masking reagent, and washing are performed to complete the first step of DNA synthesis. Then, the flow path from the condensation solvent container 8 to the synthesis reaction container 4 is switched to yet another adjustment container 1, and the same synthesis process as described above is performed.
以下この考案の特徴的構成である吸水カラム1
0部分の構成について、第2図、第3図によつて
説明する。 Below is the water absorption column 1, which is the characteristic configuration of this invention.
The configuration of the 0 portion will be explained with reference to FIGS. 2 and 3.
吸水カラム10は、カラム本体11内に吸水剤
12が設けられて構成されている。カラム本体1
1は、カラムホルダー11a内にカラムホルダー
11b端が螺入されることにより構成され、それ
ぞれのカラムホルダー11a,11bの端面の偏
心位置と中心位置にチユーブ13,13の接続口
14,14が設けられている。吸水剤12はカラ
ム本体11内の円筒空間15内の中央に、吸水カ
ラム10の軸方向に円筒状のフイルター材16内
に充填固定されて設けられている。このように吸
水剤12が位置することにより、吸水剤12は溶
媒の吸入側の接続口14に相対し、よつて排出側
の接続口14に至る間に溶媒は必ず吸水剤12内
を通つて確実に水が奪われる。 The water absorption column 10 is configured such that a water absorption agent 12 is provided within a column body 11. Column body 1
1 is constructed by screwing the end of a column holder 11b into a column holder 11a, and connection ports 14, 14 of tubes 13, 13 are provided at eccentric positions and central positions of the end faces of each column holder 11a, 11b. It is being The water-absorbing agent 12 is provided in the center of a cylindrical space 15 in the column body 11, and is filled and fixed in a cylindrical filter material 16 in the axial direction of the water-absorbing column 10. By positioning the water-absorbing agent 12 in this way, the water-absorbing agent 12 faces the connection port 14 on the solvent suction side, so that the solvent always passes through the water-absorbing agent 12 while reaching the connection port 14 on the discharge side. Water will definitely be taken away.
フイルター材16のカラム本体11内への固定
は、カラムホルダー11a,11bで両端を押圧
するようにしておこなつている。すなわち、カラ
ムホルダー11a内にカラムホルダー11bを螺
入する時に固定し、その固定の前にフイルター材
16内に吸水剤12を充填する。 The filter material 16 is fixed in the column body 11 by pressing both ends with column holders 11a and 11b. That is, when the column holder 11b is screwed into the column holder 11a, it is fixed, and before the fixation, the water absorbing agent 12 is filled into the filter material 16.
吸水剤12としては、モレキユラシーブやシリ
カゲルの微粒子を用い、フイルター材16として
は、口紙やプラスチツクフイルターや布フイルタ
ーやガラスフイルターを用いる。今、吸水剤12
として5ミクロン大のモレキユラシーブ微粒子を
用いる際には、隙間大きさが1〜2ミクロン大の
フイルター材16を用いる。このようなフイルタ
ー材16は吸水剤12を通過させず、溶媒は通過
させる。 As the water absorbing agent 12, fine particles of molecular sieve or silica gel are used, and as the filter material 16, a mouth paper, a plastic filter, a cloth filter, or a glass filter is used. Now, water absorbing agent 12
When using molecular sieve fine particles of 5 microns in size, a filter material 16 with a gap size of 1 to 2 microns is used. Such a filter material 16 does not allow the water absorbing agent 12 to pass through it, but allows the solvent to pass through it.
上記第1図のDNA等合成装置において、吸水
カラム10が調整用容器1の前段に設けられるこ
とによりDNA等合成試薬と縮合剤の混合以前に
溶媒内の水が奪われ、合成反応容器4における縮
合反応は溶媒内の水分により阻害されることがな
くおこなわれる。 In the apparatus for synthesizing DNA, etc., shown in FIG. The condensation reaction takes place without being inhibited by moisture in the solvent.
上記の第1図に示す実施例においては、DNA
等合成試薬容器と縮合剤容器とを一体とした調整
用容器を用いたが、この調整用容器は第4図に示
すようなもので、内部にフイルター17が2段に
設けられ、上部のフイルター17上が縮合剤容器
3とされ、下部のフイルター17上がDNA等合
成試薬容器2とされている。そして上方から溶媒
が流入し、下方からDNA等合成試薬と縮合剤と
が溶媒で混合された溶液が送出される。 In the embodiment shown in FIG. 1 above, DNA
We used an adjustment container that integrated a synthetic reagent container and a condensing agent container. The upper part of the filter 17 is used as a condensing agent container 3, and the lower part above the filter 17 is used as a DNA synthesis reagent container 2. Then, a solvent flows in from above, and a solution in which a synthetic reagent such as DNA and a condensing agent are mixed in a solvent is sent out from below.
また、上記の第1図に示す実施例においては、
調整用容器を用い縮合用溶媒はDNA等合成試薬
と縮合剤とを混合するように用いたが、DNA等
合成試薬、縮合剤がともにすでに溶媒に一体とさ
れているものを用いる場合には、縮合用溶媒の希
釈用溶媒として用いることが考えられ、当然その
際には縮合用溶媒剤容器および吸水カラムは適宜
位置に配置される。 Furthermore, in the embodiment shown in FIG. 1 above,
The condensation solvent was used to mix the DNA synthesis reagent and the condensation agent using an adjustment container, but if the DNA synthesis reagent and condensation agent are both already combined in the solvent, It is conceivable to use it as a diluting solvent for the condensation solvent, and in that case, the condensation solvent container and the water absorption column are naturally placed at appropriate positions.
すなわちこの考案にいう縮合用溶媒とは、縮合
の際に存在する溶媒をいい、その存在が積極的で
あるか消極的であるかは問わない。 That is, the condensation solvent referred to in this invention refers to a solvent that is present during condensation, and it does not matter whether its presence is positive or negative.
さらに第1図に示した実施例の縮合用溶媒が洗
浄や乾燥用として使用されることも考えられる。 Furthermore, it is conceivable that the condensation solvent of the embodiment shown in FIG. 1 may be used for washing and drying purposes.
(ヘ) 効果
この考案は上述のように構成されているので、
この考案によれば縮合用溶媒の水分が吸水カラム
内を通過することにより自動的に除去される。よ
つて長時間にわたつて同一の縮合用溶媒を用い、
その縮合用溶媒内に仮に水分が侵入したとしても
何ら支障がなく、同一の縮合用溶媒の長時間の連
続使用が可能となる。また吸水剤はフイルター材
によつて区画される空間内に充填されているので
溶媒内に吸水剤が混入することもない。(f) Effects This idea is structured as described above, so
According to this invention, water in the condensation solvent is automatically removed by passing through the water absorption column. Therefore, using the same condensation solvent for a long time,
Even if water were to enter the condensation solvent, there would be no problem, and the same condensation solvent could be used continuously for a long time. Furthermore, since the water-absorbing agent is filled in the space defined by the filter material, the water-absorbing agent does not mix into the solvent.
第1図はこの考案のDNA等合成装置の実施例
全体構成略図、第2図はDNA等合成装置の縮合
用溶媒容器と吸水カラム部分の実施例断面図、第
3図は吸水カラムの実施例断面図、第4図は調整
用容器の縦断面図である。
2……DNA等合成試薬容器、3……縮合剤容
器、4……合成反応容器、8……縮合用溶媒容
器、9……引き出しチユーブ、10……吸水カラ
ム、12……吸水剤。
Figure 1 is a schematic diagram of the overall configuration of an embodiment of the DNA synthesis apparatus of this invention, Figure 2 is a sectional view of an embodiment of the condensation solvent container and water absorption column of the DNA synthesis apparatus, and Figure 3 is an embodiment of the water absorption column. The cross-sectional view, FIG. 4, is a longitudinal cross-sectional view of the adjustment container. 2... DNA synthesis reagent container, 3... Condensing agent container, 4... Synthesis reaction container, 8... Condensation solvent container, 9... Drawer tube, 10... Water absorption column, 12... Water absorption agent.
Claims (1)
各種試薬容器と縮合用溶媒容器と合成反応容器と
を備え、合成反応容器内においてDNA等の合成
のなされるDNA等合成装置において、縮合用溶
媒容器から延出する縮合用溶媒の引き出しチユー
ブに、内部のフイルター材によつて区画される空
間内に吸水剤が充填された吸水カラムを組みこん
だことを特徴とするDNA等合成装置。 In a DNA synthesis apparatus that is equipped with a plurality of DNA synthesis reagent containers, a condensation agent container, various reagent containers, a condensation solvent container, and a synthesis reaction container, and in which DNA or the like is synthesized in the synthesis reaction container, the condensation solvent 1. An apparatus for synthesizing DNA, etc., characterized in that a water absorption column filled with a water absorption agent is incorporated into a condensation solvent draw-out tube extending from a container, in a space defined by an internal filter material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18502883U JPS6093733U (en) | 1983-11-29 | 1983-11-29 | DNA synthesis equipment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18502883U JPS6093733U (en) | 1983-11-29 | 1983-11-29 | DNA synthesis equipment |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6093733U JPS6093733U (en) | 1985-06-26 |
JPS6319308Y2 true JPS6319308Y2 (en) | 1988-05-30 |
Family
ID=30400025
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18502883U Granted JPS6093733U (en) | 1983-11-29 | 1983-11-29 | DNA synthesis equipment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6093733U (en) |
-
1983
- 1983-11-29 JP JP18502883U patent/JPS6093733U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6093733U (en) | 1985-06-26 |
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