Plasmids and process for producing recombinant desulphatohirudin HV-1 peptides

The present invention relates to a process for producing recombinant desulphatohirudin by means of culturing microorganisms. Concerning the codon usage of microorganisms the synthesized nucleotide sequences were joined downstream of and in reading frame with isolated promoters and signal sequences,...

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Hauptverfasser: ERDEI, J+E,ACU A+EE NOS, BARK+E,ACU O+EE N+E,ACU E+EE E T+E,ACU O+EE TH, ZSUZSA, MORAVCSIK, IMRE, VINCZE, ATTILA, KISS, GY+E,UML O+EE RGY B, TEGDES, ANIK+E,ACU O+EE, M+E,ACU A+EE T+E,ACU E+EE, GY+E,UML O+EE RGY, KLUPP, TIBOR, P+E,ACU O+EE LYA, K+E,ACU A+EE LM+E,ACU A+EE N, K+E,UML O+EE NCZ+E,UML O+EE L, GULY+E,ACU A+EE S, +E,ACU E+EE VA, ZILAHI, ERIKA, AMBRUS, G+E,ACU A+EE BOR, OTT, ISTV+E,ACU A+EE N, BARAB+E,ACU A+EE S, BARTA, ALBRECHT, K+E,ACU A+EE RNLY, P+E,ACU E+EE TER, MOLN+E,ACU A+EE R, EGY+E,UML U+EE D, CECILIA, SAL+E,ACU A+EE T, PATTHY, ANDR+E,ACU A+EE S
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creator ERDEI
J+E,ACU A+EE NOS
BARK+E,ACU O+EE N+E,ACU E+EE E T+E,ACU O+EE TH
ZSUZSA
MORAVCSIK
IMRE
VINCZE
ATTILA
KISS
GY+E,UML O+EE RGY B
TEGDES
ANIK+E,ACU O+EE
M+E,ACU A+EE T+E,ACU E+EE
GY+E,UML O+EE RGY
KLUPP
TIBOR
P+E,ACU O+EE LYA
K+E,ACU A+EE LM+E,ACU A+EE N
K+E,UML O+EE NCZ+E,UML O+EE L
K+E,ACU A+EE LM+E,ACU A+EE N
GULY+E,ACU A+EE S
+E,ACU E+EE VA
ZILAHI
ERIKA
AMBRUS
G+E,ACU A+EE BOR
OTT
ISTV+E,ACU A+EE N
BARAB+E,ACU A+EE S
+E,ACU E+EE VA
BARTA
ISTV+E,ACU A+EE N
ALBRECHT
K+E,ACU A+EE RNLY
KISS
P+E,ACU E+EE TER
MOLN+E,ACU A+EE R
ISTV+E,ACU A+EE N
EGY+E,UML U+EE D
CECILIA
SAL+E,ACU A+EE T
J+E,ACU A+EE NOS
PATTHY
ANDR+E,ACU A+EE S
description The present invention relates to a process for producing recombinant desulphatohirudin by means of culturing microorganisms. Concerning the codon usage of microorganisms the synthesized nucleotide sequences were joined downstream of and in reading frame with isolated promoters and signal sequences, subsequently the expression/secretion cassettes comprising the foregoing elements were inserted into plasmid DNAs allowing the cultivation of cells under selective culture conditions. E. coli, Saccharomyces and Streptomyces species were transformed with the said recombinant plasmids to biosynthesize the thrombin inhibitor desulphatohirudin HV-1 which was then isolated and identified. The thus-produced desulphatohirudin can be used to inhibit blood coagulation.
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Concerning the codon usage of microorganisms the synthesized nucleotide sequences were joined downstream of and in reading frame with isolated promoters and signal sequences, subsequently the expression/secretion cassettes comprising the foregoing elements were inserted into plasmid DNAs allowing the cultivation of cells under selective culture conditions. E. coli, Saccharomyces and Streptomyces species were transformed with the said recombinant plasmids to biosynthesize the thrombin inhibitor desulphatohirudin HV-1 which was then isolated and identified. The thus-produced desulphatohirudin can be used to inhibit blood coagulation.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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language eng
recordid cdi_epo_espacenet_US5552299A
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subjects BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS THEREOF
CULTURE MEDIA
ENZYMOLOGY
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
MICROBIOLOGY
MICROORGANISMS OR ENZYMES
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
PEPTIDES
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS
SPIRITS
VINEGAR
WINE
title Plasmids and process for producing recombinant desulphatohirudin HV-1 peptides
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