Patent US4434228A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4434228A Expired / Lapsed US ⏱️ 0.0 years remaining

Immobilization of biological materials in condensed polyalkyleneimine polymers

Assignee: Genex Corp
•
Filing: 1982-04-20
•
Granted: 1984-02-28
•
Expires: 2002-04-20
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Biological materials are immobilized within condensed polyalkyleneimine polymers. Condensation of the polymer is accomplished by bridging the amine groups of polyalkyleneimine polymer chains with a polycarboxylic acid, in the presence of a condensing agent. d

Inventors

  • 👤 Wayne E. Swann

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 08:47
CPC Classifications
C; C12; C12P; C12P13/00; C12P13/04; C12P13/22; C12N; C12N11/00; C12N11/02; C12N11/08; C12N11/089; C12N11/098; C12P13/20

Claims Analysis

Total Claims: 39
Claim 1
Independent Claim 52 words
A method for immobilizing a biological material by preparing an insolubilized biological material composite, comprising condensing a polyalkyleneimine polymer with a condensing amount of a polycarboxylic acid in the presence of a condensing amount of a condensing agent, wherein said biological material is mixed with said polyalkyleneimine polymer during said condensation reaction.
Claim 2
Independent Claim 52 words
A method for immobilizing a biological material by preparing an insolubilized biological material composite, comprising condensing a polyalkyleneimine polymer with a condensing amount of a polycarboxylic acid in the presence of a condensing amount of a condensing agent, wherein said biological material is mixed with said polyalkyleneimine polymer during said condensation reaction.
Claim 3
Dependent Claim 21 words
The method of claim 1, wherein the polyalkyleneimine polymer is selected from the group consisting of polyethyleneimine, polypropyleneimine, polybutyleneimine and polypentyleneimine.
Claim 4
Dependent Claim 11 words
The method of claim 1, wherein the polyalkylenemine polymer is polyethyleneimine.
Claim 5
Dependent Claim 13 words
The method of claim 1, wherein the polycarboxylic acid is a dicarboxylic acid.
Claim 6
Dependent Claim 40 words
The method of claim 1, 2 or 3 wherein the polycarboxylic acid is selected from the group consisting of adipic, azelaic, 1,11-undecanedioic, 1,12-dodecanedioic, traumatic, pentadecanedioic, hexadecanedioic, sebacic, suberic, glutaric, malonic, pimellic, succinic, malic, maleic, glutamic, aspartic, oxalic, fumaric, and polyaspartic.
Claim 7
Dependent Claim 15 words
The method of claim 1, 2 or 3 wherein the polycarboxylic acid is succinic acid.
Claim 8
Dependent Claim 18 words
The method of claim 1 wherein the condensing agent is selected from the group consisting of N-ethyl-5-phenylisoxazolium-3-sulfonate, N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline.
Claim 9
Dependent Claim 14 words
The method of claim 1 wherein the condensing agent is a carbodiimide condensing agent.
Claim 10
Dependent Claim 23 words
The method of claim 8, wherein the carbodiimide condensing agent is 1-ethyl-3,3-dimethylaminopropyl carbodiimide, dicyclohexyl carbodiimide, 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate, or a salt thereof.
Claim 11
Dependent Claim 17 words
The method of claim 1, wherein the carbodiimide condensing agent is 1-ethyl-3,3-dimethylaminopropyl carbodimide or a salt thereof.
Claim 12
Dependent Claim 16 words
The method of claim 5 wherein the condensing agent is 1-ethyl-3,3-dimethylaminopropyl carbodiimide or a salt thereof.
Claim 13
Dependent Claim 23 words
The method of claim 1, 2, 3 or 4, wherein the molar ratio of polyalkyleneimine to polycarboxylic is from about 1:20 to 1:0005.
Claim 14
Dependent Claim 27 words
The method of claim 12, wherein the condensing agent is employed in an amount ranging from about 0.2 to 3 times stoichiometric, relative to the polycarboxylic acid.
Claim 15
Dependent Claim 27 words
The method of claim 12, wherein the condensing agent is employed in an amount ranging from about 0.5 to 1.5 times stoichiometric relative to the polycarboxylic acid.
Claim 16
Dependent Claim 30 words
The method of claim 1, 2, 3 or 4 wherein the polyalkyleneimine and polycarboxylic acid are first mixed, then the biological material is added, then the condensing agent is added.
Claim 17
Dependent Claim 13 words
The method of claim 1, wherein the biological material immobilized is an enzyme.
Claim 18
Dependent Claim 13 words
The method of claim 1, wherein the biological material immobilized comprises whole cells.
Claim 19
Dependent Claim 16 words
The method of claim 17, wherein the whole cells are E. coli cells which contain aspartase.
Claim 20
Dependent Claim 11 words
The method of claim 9, wherein the biological material is aspartase.
Claim 21
Dependent Claim 12 words
The method of claim 1, wherein the biological material comprises phenylalanine ammonia-lyase.
Claim 22
Dependent Claim 12 words
The method of claim 1, wherein the biological material comprises tryptophan synthetase.
Claim 23
Dependent Claim 29 words
The method of claim 1, further comprising post treatment of the insolubilized biological material composite with an amine crosslinking agent to impart additional strength and stability to the composite.
Claim 24
Dependent Claim 27 words
The method of claim 22, wherein the amine crosslinking agent is selected from the group consisting of glutaric dialdehyde, diisocyanates, polyisocyanates, 2,4,6-trichloro-S-triazine, bisoxirane, bisimidate, divinylsulfone, and 1,5-difluoro-2,4-dinitrobenzene.
Claim 25
Dependent Claim 13 words
The method of claim 22, wherein the amine crosslinking agent is glutaric dialdehyde.
Claim 26
Dependent Claim 29 words
An insolubilized biological material composite comprising a biologically active material immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine chains are bridged by a polycarboxylic acid.
Claim 27
Dependent Claim 29 words
An insolubilized biological material composite comprising a biologically active material immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine chains are bridged by a polycarboxylic acid.
Claim 28
Dependent Claim 31 words
The composite of claim 25, wherein the biologically active material is selected from the group consisting of enzymes, antigens, antibodies, antibiotics, carbohydrates, coenzymes, plant cells, bacteria, yeast, fungi and tissue cultures.
Claim 29
Dependent Claim 21 words
The composite of claim 25, wherein the biologically active material is selected from the group consisting of enzymes and whole cells.
Claim 30
Dependent Claim 12 words
The composite of claim 25, wherein the biologically active material is aspartase.
Claim 31
Dependent Claim 18 words
The composite of claim 25, wherein the biological material are whole cells of E. coli which contain aspartase.
Claim 32
Dependent Claim 12 words
The composite of claim 25, wherein the biological material comprises phenylalanine ammonia-lyase.
Claim 33
Dependent Claim 12 words
The composite of claim 25, wherein the biological material comprises tryptophan synthetase.
Claim 34
Independent Claim 49 words
A method for producing aspartic acid, comprising contacting, under aspartic acid-producing conditions, a substrate, containing ammonium fumarate, with an insolubilized biological material composite of aspartase or aspartase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.
Claim 35
Independent Claim 49 words
A method for producing aspartic acid, comprising contacting, under aspartic acid-producing conditions, a substrate, containing ammonium fumarate, with an insolubilized biological material composite of aspartase or aspartase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.
Claim 36
Independent Claim 51 words
A method for producing phenylalanine, comprising contacting, under phenylalanine-producing conditions, a substrate, containing t-cinnamic acid and ammonia, with an insolubilized biological material composite of phenylalanine ammonia-lyase or phenylalanine ammonia-lyase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.
Claim 37
Independent Claim 51 words
A method for producing phenylalanine, comprising contacting, under phenylalanine-producing conditions, a substrate, containing t-cinnamic acid and ammonia, with an insolubilized biological material composite of phenylalanine ammonia-lyase or phenylalanine ammonia-lyase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.
Claim 38
Independent Claim 49 words
A method for producing tryptophan, comprising contacting, under tryptophan-producing conditions, a substrate, containing indole and serine, with an insolubilized biological material composite of tryptophan synthetase or tryptophan-synthetase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.
Claim 39
Independent Claim 49 words
A method for producing tryptophan, comprising contacting, under tryptophan-producing conditions, a substrate, containing indole and serine, with an insolubilized biological material composite of tryptophan synthetase or tryptophan-synthetase-containing microbial cells immobilized within a condensed polyalkyleneimine polymer, wherein amino groups on the polyalkyleneimine polymer chains are bridged by a polycarboxylic acid.

References Cited (Backward Citations)

US3791926A Cited
GB1396714A Cited
US3830699A Cited
US3859169A Cited
US4182695A Cited
GB2019410B Cited
US4248969A Cited
US4355105A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-02-27 1987-08-29 1988-02-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-02-27 1991-08-29 1992-02-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-02-27 1995-08-29 1996-02-28 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag