{"id":8105,"date":"2024-08-11T19:11:51","date_gmt":"2024-08-11T19:11:51","guid":{"rendered":"https:\/\/longchangextracts.com\/?p=8105"},"modified":"2024-08-11T19:11:51","modified_gmt":"2024-08-11T19:11:51","slug":"bingchengensis-bcj60","status":"publish","type":"post","link":"https:\/\/longchangextracts.com\/de\/bingchengensis-bcj60\/","title":{"rendered":"Studie \u00fcber Sekund\u00e4rmetaboliten des gentechnisch ver\u00e4nderten Bakteriums Streptomyces bingchengensis BCJ60"},"content":{"rendered":"<p>Studie \u00fcber Sekund\u00e4rmetaboliten des gentechnisch ver\u00e4nderten Bakteriums Streptomyces bingchengensis BCJ60<br \/>\nPolyketidverbindungen sind eine Art von Naturprodukten, die durch kontinuierliche Kondensationsreaktionen von niederen Carbons\u00e4uren, katalysiert durch die Polyketidsynthase, hergestellt werden, darunter Makrolide, Tetracycline, Anthrachinone und Polyether. Aus pharmakologischer Sicht sind Polyketidverbindungen eine wichtige Quelle f\u00fcr neuartige Arzneimittel, die haupts\u00e4chlich als Antibiotika, Immunsuppressiva, Antiparasitika, Cholesterinsenker und Antitumormittel eingesetzt werden. Die Funktion jeder Dom\u00e4ne der Polyketidsynthase entspricht der Struktur des Endprodukts. Diese Korrespondenz kann daher genutzt werden, um Biosynthesegene zu bearbeiten und synthetische Produkte zu entwerfen, wodurch ein neues Forschungsgebiet entsteht - die kombinatorische Biologie der Polyketidsynthase. Die Wissenschaftler erzeugen neue Produkte vor allem durch die Reduzierung, Vergr\u00f6\u00dferung oder den Austausch von Modulen und Strukturbereichen der Polyketidsynthase, beispielsweise durch die Ver\u00e4nderung des Polyketidsynthase-Genclusters aveLAT-ACP in Streptomyces avermitilis, um einen gentechnisch ver\u00e4nderten Stamm zu erhalten. Zwei neue Avermectin-Derivate, 25-Methyl-Ivermectin und 25-Ethyl-Ivermectin, wurden aus den Sekund\u00e4rmetaboliten des Stammes isoliert.<\/p>\n<p>In fr\u00fcheren Forschungsarbeiten hat unsere Forschungsgruppe das milF-Gen, das f\u00fcr die Polyketidsynthase in Streptomyces bingchengensis BC-120-4 kodiert, ver\u00e4ndert, um den gentechnisch ver\u00e4nderten Stamm Streptomyces bingchengensis BCJ60 zu erhalten. Dieser Stamm kann nicht f\u00fcr C-5-Ketoreduktase kodieren und blockiert somit die Synthese von Milbeimycin A3\/A4\/B2\/B3. Durch eine gezielte genetische Ver\u00e4nderung kann das biosynthetische Gencluster ver\u00e4ndert werden, wodurch bestimmte biosynthetische Wege zur Gewinnung neuer Metaboliten aktiviert werden k\u00f6nnen. Daher konzentriert sich diese Studie haupts\u00e4chlich auf die Sekund\u00e4rmetaboliten des gentechnisch ver\u00e4nderten Stammes Streptomyces bingchengensis BCJ60, um hochwirksame insektizide Antibiotika mit praktischem Wert zu erhalten.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>In diesem Artikel werden die Sekund\u00e4rmetaboliten des gentechnisch ver\u00e4nderten Bakteriums Streptomyces bingchengensis BCJ60 systematisch untersucht, und es wurden 11 Verbindungen gewonnen, von denen die Verbindungen 1 und 2 zwei neue Verbindungen sind. In fr\u00fcheren Studien hat unsere Forschungsgruppe Voruntersuchungen zu den Sekund\u00e4rmetaboliten des gentechnisch ver\u00e4nderten Bakteriums Streptomyces bingchengensis BCJ60 durchgef\u00fchrt und 12 neue Verbindungen erhalten, bei denen es sich um Milberelline handelt. Dies deutet darauf hin, dass durch die gezielte Ver\u00e4nderung von Genen das biosynthetische Gencluster ver\u00e4ndert wird, wodurch bestimmte Biosynthesewege aktiviert und neue Metaboliten gewonnen werden, was zum weiteren Verst\u00e4ndnis des Biosynthesemechanismus von Mirella-Verbindungen beitr\u00e4gt. Das Experiment zur insektiziden Aktivit\u00e4t der neuen Verbindung zeigte, dass die Verbindungen 1 und 2 eine signifikante Abt\u00f6tungsaktivit\u00e4t gegen Zinnobermilben und Kiefernholznematoden aufwiesen, wobei kein signifikanter Unterschied zu dem kommerziellen Mirbeimycin A3\/A4 bestand. Dies deutet darauf hin, dass die Verbindungen 1 und 2 nicht nur als alternative Insektizide zu Mirbeimycin A3\/A4 dienen k\u00f6nnen, sondern auch das Potenzial haben, eine neue Generation von Agrar- oder Veterin\u00e4rantibiotika mit h\u00f6herer Aktivit\u00e4t durch strukturelle Ver\u00e4nderung zu erhalten.<\/p>","protected":false},"excerpt":{"rendered":"<p>Study on secondary metabolites of genetically engineered bacterium Streptomyces bingchengensis BCJ60 Polyketide compounds are a type of natural product produced by continuous condensation reactions of lower carboxylic acids catalyzed by polyketide synthase, including macrolides, tetracyclines, anthraquinones, and polyethers. From a pharmacological perspective, polyketide compounds are an important source of novel drugs, mainly used as antibiotics, [&hellip;]<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Study on secondary metabolites of genetically engineered bacterium Streptomyces bingchengensis BCJ60 - China Chemical Manufacturer<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/longchangextracts.com\/de\/bingchengensis-bcj60\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Study on secondary metabolites of genetically engineered bacterium Streptomyces bingchengensis BCJ60 - China Chemical Manufacturer\" \/>\n<meta property=\"og:description\" content=\"Study on secondary metabolites of genetically engineered bacterium Streptomyces bingchengensis BCJ60 Polyketide compounds are a type of natural product produced by continuous condensation reactions of lower carboxylic acids catalyzed by polyketide synthase, including macrolides, tetracyclines, anthraquinones, and polyethers. 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