Abstract:
The present invention relates to an FRET donor/acceptor pair for use as biosensor, comprising at least two fluorescence proteins, where at least one fluorescence protein is stable with respect to a parameter to be detected by the biosensor and at least one fluorescence protein is not stable.
Abstract:
Die vorliegende Erfindung betrifft die Verwendung eines Proteins umfassend eine LOV-Domäne zur photosensiblen Desfunktionalisierung eines Moleküls sowie eine Methode zur photosensiblen Desfunktionalisierung eines Zielmoleküls.
Abstract:
The invention relates to compounds exhibiting an antibiotic activity which are extracted from body fluids of mollusks, namely from certain West African snails. The invention also relates to medicaments comprising these compounds and to the application thereof for producing a medicament used to control infectious pathogens in humans and animals.
Abstract:
Zur Untersuchung von Protein-Protein Interaktionen, Proteinfaltungen und Proteinlokalisation sowie bei der Sekretion von Proteinen werden in der Biotechnologie und in der Grundlagenforschung in vivo Reporterproteine eingesetzt. Um Fluoreszenzreporter als Marker für Sekretionsprozesse nutzen zu können, wurden von uns erstmals FMN-bindende Fluoreszenproteine (FbFP) entwickelt. Die neuen Fluoreszenzmarker lassen sich wie GFP in verschiedenen Bakterien exprimieren. Durch die Bindung des Chromophors FMN entsteht so ein cyan-grün fluoreszierendes Protein, das sich in vivo mit allen gängigen spektroskopischen und mikroskopischen Verfahren nachweisen lässt. Im Gegensatz zu GFP kann dieses Protein überraschender Weise auch über den Sec-Weg sekretiert und im Periplasma in den fluoreszenzaktiven Zustand überführt werden.
Abstract:
Die vorliegende Erfindung betrifft ein FRET-Donor-Akzeptor-Paar zur Verwendung als Biosensor umfassend mindestens zwei Fluoreszenzproteine, wobei wenigstens ein Fluoreszenzprotein gegenber einem durch den Biosensor zur detektierenden Parameter stabil und mindestens eins nicht stabil ist.
Abstract:
The present invention relates to a polynucleotide encoding an enzyme having carboxyl esterase [E. C. 3.1.1.1] activity, wherein the coding sequence is selected from the group consisting of (a) a polynucleotide encoding an amino acid sequence as depicted in any one of SEQ ID NOs: 2, 4, 6 and 8; (b) a polynucleotide having or comprising a nucleotide sequence encoding an enzyme, wherein the nucleic acid sequence is as shown in any one of SEQ ID NOs: 1, 3, 5 and 7; (c) a polynucleotide having or comprising a nucleotide sequence encoding a fragment or derivative of an enzyme encoded by a polynucleotide of (a) or (b), wherein in said derivative one or more amino acid residues are conservatively substituted compared to the amino acid sequence of (a); (d) a polynucleotide encoding an enzyme having carboxyl esterase activity which polynucleotide is at least 65% identical to a polynucleotide encoding an enzyme as shown in one of SEQ ID NOs: 2, 4, 6 and 8; (e) a polynucleotide having or comprising a nucleotide sequence the complementary strand of which hybridizes to a polynucleotide as defined in any one of (a) to (d); and (T) a polynucleotide having or comprising a nucleotide sequence being degenerate to the nucleotide sequence of the polynucleotide of (d) or (e); or the complementary strand of such a polynucleotide of (a) to (f) or fragments thereof useful as specific probes or primers. The present invention also relates to a host, genetically engineered with the polynucleotide of the present invention or the vector of the present invention. The present invention also relates to a polypeptide comprising the amino acid sequence encoded by a polynucleotide of the present invention or which is obtainable by the process of the present invention. Moreover, the present invention relates to a process for producing said polypeptide and for producing bacteria expressing said polypeptide. Finally, the present invention relates to a composition comprising the polynucleotide of the present invention, the vector of the present invention, the host of the present invention, the polypeptide of the present invention, the antibody of the present invention and/or one or more primers of the present invention.
Abstract translation:本发明涉及编码具有羧基酯酶[E. 3.1.1.1]活性,其中编码序列选自(a)编码SEQ ID NO:2,4,6和8中任一个所示氨基酸序列的多核苷酸; (b)具有或包含编码酶的核苷酸序列的多核苷酸,其中所述核酸序列如SEQ ID NO:1,3,5和7中任一个所示; (c)具有或包含编码由(a)或(b)的多核苷酸编码的酶的片段或衍生物的核苷酸序列的多核苷酸,其中在所述衍生物中,与氨基酸相比,一个或多个氨基酸残基被保守取代 (a)的顺序; (d)编码具有羧基酯酶活性的酶的多核苷酸与编码如SEQ ID NO:2,4,6和8之一所示的酶的多核苷酸至少65%相同; (e)具有或包含核苷酸序列的多核苷酸,其互补链与(a)至(d)中任一项所定义的多核苷酸杂交; 和(T)具有或包含与(d)或(e)的多核苷酸的核苷酸序列退化的核苷酸序列的多核苷酸; 或(a)至(f)的这种多核苷酸或其片段的互补链用作特异性探针或引物。 本发明还涉及用本发明的多核苷酸或本发明的载体进行遗传工程改造的宿主。 本发明还涉及包含由本发明的多核苷酸编码或可通过本发明的方法获得的氨基酸序列的多肽。 此外,本发明涉及生产所述多肽和产生表达所述多肽的细菌的方法。 最后,本发明涉及包含本发明的多核苷酸,本发明的载体,本发明的宿主,本发明的多肽,本发明的抗体和/或一种或多种的组合物 本发明的引物。
Abstract:
The present invention relates to a polynucleotide encoding an enzyme having carboxyl esterase [E. C. 3.1.1.1] activity, wherein the coding sequence is selected from the group consisting of (a) a polynucleotide encoding an amino acid sequence as depicted in any one of SEQ ID NOs: 2, 4, 6 and 8; (b) a polynucleotide having or comprising a nucleotide sequence encoding an enzyme, wherein the nucleic acid sequence is as shown in any one of SEQ ID NOs: 1, 3, 5 and 7; (c) a polynucleotide having or comprising a nucleotide sequence encoding a fragment or derivative of an enzyme encoded by a polynucleotide of (a) or (b), wherein in said derivative one or more amino acid residues are conservatively substituted compared to the amino acid sequence of (a); (d) a polynucleotide encoding an enzyme having carboxyl esterase activity which polynucleotide is at least 65% identical to a polynucleotide encoding an enzyme as shown in one of SEQ ID NOs: 2, 4, 6 and 8; (e) a polynucleotide having or comprising a nucleotide sequence the complementary strand of which hybridizes to a polynucleotide as defined in any one of (a) to (d); and (T) a polynucleotide having or comprising a nucleotide sequence being degenerate to the nucleotide sequence of the polynucleotide of (d) or (e); or the complementary strand of such a polynucleotide of (a) to (f) or fragments thereof useful as specific probes or primers. The present invention also relates to a host, genetically engineered with the polynucleotide of the present invention or the vector of the present invention. The present invention also relates to a polypeptide comprising the amino acid sequence encoded by a polynucleotide of the present invention or which is obtainable by the process of the present invention. Moreover, the present invention relates to a process for producing said polypeptide and for producing bacteria expressing said polypeptide. Finally, the present invention relates to a composition comprising the polynucleotide of the present invention, the vector of the present invention, the host of the present invention, the polypeptide of the present invention, the antibody of the present invention and/or one or more primers of the present invention.
Abstract translation:本发明涉及编码具有羧基酯酶[E. 3.1.1.1]活性,其中编码序列选自(a)编码SEQ ID NO:2,4,6和8中任一个所示氨基酸序列的多核苷酸; (b)具有或包含编码酶的核苷酸序列的多核苷酸,其中所述核酸序列如SEQ ID NO:1,3,5和7中任一个所示; (c)具有或包含编码由(a)或(b)的多核苷酸编码的酶的片段或衍生物的核苷酸序列的多核苷酸,其中在所述衍生物中,与氨基酸相比,一个或多个氨基酸残基被保守取代 (a)的顺序; (d)编码具有羧基酯酶活性的酶的多核苷酸与编码如SEQ ID NO:2,4,6和8之一所示的酶的多核苷酸至少65%相同; (e)具有或包含核苷酸序列的多核苷酸,其互补链与(a)至(d)中任一项所定义的多核苷酸杂交; 和(T)具有或包含与(d)或(e)的多核苷酸的核苷酸序列退化的核苷酸序列的多核苷酸; 或(a)至(f)的这种多核苷酸或其片段的互补链用作特异性探针或引物。 本发明还涉及用本发明的多核苷酸或本发明的载体进行遗传工程改造的宿主。 本发明还涉及包含由本发明的多核苷酸编码或可通过本发明的方法获得的氨基酸序列的多肽。 此外,本发明涉及生产所述多肽和产生表达所述多肽的细菌的方法。 最后,本发明涉及包含本发明的多核苷酸,本发明的载体,本发明的宿主,本发明的多肽,本发明的抗体和/或一种或多种的组合物 本发明的引物。
Abstract:
The invention relates to novel proteins, in particular, exhibiting a protease activity and promoting the production of extracellular lipases by bacteria, in particular, by Burkholderia-type bacteria, to coding nucleic acid sequences, expression constructs containing them, host modified thereby, to a method for producing proteins exhibiting a protease activity and to a lipase production method, in particular by Burkholderia-type bacteria.
Abstract:
The invention relates to agents containing esterases, and to the use thereof for dressing fibres, in particular, artificial fibres, washing and cleaning agents comprising esterases and corresponding washing and cleaning methods, in addition to additional technical areas of application. The invention also relates to the use of esterases for protecting against or reducing and/or preventing pilling, preferably in textiles, particularly plastic fibres, more preferably polyester fibres, in addition to the use of esterases for separating the plastics, in particular, polyester compounds. The invention further relates to novel esterases and to sufficiently related proteins and to derivatives thereof, agents containing them and to the use thereof.
Abstract:
The invention relates to a method for producing and identifying hydrolase mutants having improved properties regarding stereoselectivity and site selectivity, catalytic activity or stability during chemical reactions.