CS268591B1 - The method of obtaining enzymes from the feraentation base of penicillin production ultra f 1 lt rieloti - Google Patents
The method of obtaining enzymes from the feraentation base of penicillin production ultra f 1 lt rieloti Download PDFInfo
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- CS268591B1 CS268591B1 CS88526A CS52688A CS268591B1 CS 268591 B1 CS268591 B1 CS 268591B1 CS 88526 A CS88526 A CS 88526A CS 52688 A CS52688 A CS 52688A CS 268591 B1 CS268591 B1 CS 268591B1
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Abstract
Óčeloa rltienla ja zlskavanle enzýa^v, predovietkýa proteAz z Feraentačnej pody z výroby penicilinu poaocou ultraFIltrAde. UltraflltrAclou Ja aoinA tlete vo ťlnAlnoa výrobku nežledúce látky z Feraentačnej pody Izolovat a «koncentrovat tak, ie doslahnu koncentrAdu , v ktorej sú prleayslove vyuilteínA. Súčasne sa u 11 ra F 111 r A cl ou vyčisti od neiladůdch aakroaolekutArnyeh lAtok Flnitny výrobok penicilín.The purpose of the ultrafiltration is to remove enzymes, especially proteins, from the fermentation broth of penicillin production by ultrafiltration. Ultrafiltration is used to isolate and concentrate undesirable substances from the fermentation broth in the final product to a concentration in which they are practically useful. At the same time, the final product penicillin is purified from undesirable and acroaceutical substances.
Description
CS 268 591 B1 1EN 268 591 B1 1
Vynálet riell zlskavanle prleayselne použitelných enzýaov z feraentačnej pódy z vý-roby penicilinu pomocou ult rafl lt řáde.Inventing a commercially useful enzymes from feraentative pellets from penicillin production by ultra raffle.
Feraentsčná výroba benzylpenle1l1nu a fenoxyaetylpěnidllnu sa robi subaerzne po- ocou kutěna Penldlllua chrysogenua. Hlavnýa uhlíkatým zdrojoa feraentačnej pódy je u-charóza, glukóza, alebo laktóza, zdrojoa dualka je kukuřičný extrakt, blelkovlnové sub-stráty, araíldová aúka a sojové aúka. Okrem toho póda obsahuje stopové prvky, biologic-ky aktivně látky, prekurzory, pufrujúce látky, odpeňovadlá.The pharmaceutical production of benzylpeniline and phenoxyethyl ethylidone is carried out subaerially by the Penldlllua chrysogen. The main carbon source and the feraentative post are u-charose, glucose, or lactose, the source is corn extract, bleach sub-strata, acacia and soybean. In addition, the pod contains trace elements, biologically active substances, precursors, buffering agents, defoamers.
Kultlváde prebleha prl teplote 25 °C, pH sa pohybuje v rozaedzl 6 - 7,5. Počasferaentáde sa póda Intenzivně aleča a vzduánl. Doba kultlváde je 5 - 8 dni. Po skonče-ni feraentačného procesu sa feraentačná aádlua filtruje na kolollsoch, alebo rotačnýchvákuových flltroch za účeloa odstránenla nerozpustných látok.The culture was filled at 25 ° C, the pH ranged from 6 to 7.5. The stage is intensely alive and airy. The culture time is 5-8 days. After the feraeration process has been completed, the feraentation adultera is filtered on wheels or rotary flasks to remove insoluble matter.
Počas kultlváde produkčný kaen vytvára vedla penicilinu eite ďalSie látky aedzlnlal aj extracelulárne enzýay, ktorých přítomnost vo flnálnoa výrobku je nežladúca,nakotko aóžu neprlaznlvo pósoblt na obzvláál citlivých paclentov. T1eto látky Je možno z feraentačnej pódy po skončeni kultlváde oddělit ultrafll-tráclou cez ultraf1ltračnů aeabránu s dellacou hranlcou 5 000 - 50 000 aolekulovej hmot-nosti, ktorá zadržlave vysokoaolekulárne látky a naopak prepůáta n1zkoaolekulárne zlož- fi ky feraentačnej pody. Z koncentrátu vysokoaolekulárnych látok získaného pomocou ultraf1ltráde je aožnézískávat vlaceré prleayselne významné enzýay, hlavně proteázy, T1eto enzýay, ktoré sastanů takto vedlajila produktoa výroby penicilinu sa doteraz nijako nevyužlvajů a nao-pak ako cudzorodé látky sposobujů alerglu nlektorých paclentov, sů vo flnálnoa výrobkuna závadu. ř Přiklad 1 1 000 000 dielov feraentačnej pódy z výroby benzyl penicilinu obsahujůcej 1 dlelenzýaov ultraf 11trujeae cez ultraf1Itračnů aeabránu s dellacou hranlcou 10 000 aoleku-lovej hmotnosti pr1 teplote 25 °C a tlaku 0,3 HPa. Prltoa sa cez aeabránu oddělí995 000 dielov peraeátu obsahujůceho nlzkoaolekulárne látky a nad aeabránou zostane5 000 dielov koncentrátu obsahujůdch 1 dlel enzýaov. Vyčištěný peraeát zbavený vysoko-aol ekul á rnych látok sa použije na výrobu benzylpenld11 nu. Koncentrát z ultraf11trádesa použije na výrobu enzýaov. Přiklad 2 1 000 000 dielov feraentačnej pódy z výroby fenoxyaetylpenldllnu obsahujůcej 5dielov enzýaov ultraf1ltrujeae cez ultraflItračnů aeabránu s dellacou hranlcou 20 000aolekulovej haotnoatl pr1 teplote 15 °C a tlaku 0,4 MPa. Prltoa sa cez aeabránu oddělí990 000 dielov peraeátu obsahujůceho nlzkoaolekulárne látky a nad aeabránou zostane10 000 dielov koncentrátu obsahujůdch 5 dielov enzýaov. Vyčištěný peraeát zbavený vy-sokoaolekulárnych látok sa použije na výrobu fenoxyaetylpěnid11 nu. Koncentrát sa pou-žije na výrobu enzýaov.During the culture, the production kaen forms a penicillin eite with additional substances and also extracellular enzymes, the presence of which in the product and the product is non-sweet, to the extent that it does not cure to particularly sensitive substances. These substances can be separated from the feraentation stage by ultrafiltration through an ultrafiltration and a membrane with a separating edge of 5,000 - 50,000 and molecular weight, which retains the high molecular weight substances and, on the other hand, transfers the low molecular weight components of the phaeractic substrate. From the high molecular weight concentrate obtained by ultrafiltration, it is possible to obtain, in the meantime, importantly important enzymes, especially proteases. EXAMPLE 1 1 000 000 parts of a benzyl penicillin feraentation process containing 1 x ultrafilera ultrafiltration through ultrafiltration and a membrane with a 10,000 molecular weight cutoff at 25 ° C and 0.3 HPa pressure. The extrudate is separated by 995,000 parts percolate containing a low molecular weight substance and 5,000 parts of the concentrate containing 1 µl of enzyme are left over the membrane. Purified peracyl free peracid was used to produce benzylpiperidine. The ultrafiltrate concentrate is used to produce enzymes. Example 2 1 000 000 parts of a phenoxy-ethyl-pennyl feraentation filter containing 5 parts of ultrafiltrate enzymes via ultrafiltration and a barrier having a 20,000-molecular haotnoatl cut-off at a temperature of 15 ° C and a pressure of 0.4 MPa. The flow is separated by aO000,000 parts percolate containing a low molecular weight substance and 10,000 parts of the concentrate containing 5 parts of the enzyme remain above the membrane. The purified percolate-free peracetic acid was used to produce phenoxy-ethylpolymer. The concentrate is used for the production of enzymes.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS88526A CS268591B1 (en) | 1988-01-28 | 1988-01-28 | The method of obtaining enzymes from the feraentation base of penicillin production ultra f 1 lt rieloti |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS88526A CS268591B1 (en) | 1988-01-28 | 1988-01-28 | The method of obtaining enzymes from the feraentation base of penicillin production ultra f 1 lt rieloti |
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| Publication Number | Publication Date |
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| CS52688A1 CS52688A1 (en) | 1989-08-14 |
| CS268591B1 true CS268591B1 (en) | 1990-03-14 |
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| Application Number | Title | Priority Date | Filing Date |
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| CS88526A CS268591B1 (en) | 1988-01-28 | 1988-01-28 | The method of obtaining enzymes from the feraentation base of penicillin production ultra f 1 lt rieloti |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2105988A1 (en) * | 1996-03-15 | 1997-10-16 | Antibioticos Sa | Process for purifying 7-substituted-amino-desacetoxy-cephalosporines through the use of filtration membranes |
-
1988
- 1988-01-28 CS CS88526A patent/CS268591B1/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2105988A1 (en) * | 1996-03-15 | 1997-10-16 | Antibioticos Sa | Process for purifying 7-substituted-amino-desacetoxy-cephalosporines through the use of filtration membranes |
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| Publication number | Publication date |
|---|---|
| CS52688A1 (en) | 1989-08-14 |
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