Klonování PCB degradujícího bakteriálního genu do rostlin

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F04%3A00012752" target="_blank" >RIV/60461373:22330/04:00012752 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/60461373:22330/04:00017137

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Cloning of bacterial PCB degradative genes to plants

Popis výsledku v původním jazyce

The target of this work is to increase biodegradation of polychlorinated biphenyls (PCBs) by the plants transformed with the gene from bacterial PCB degradation pathway. Bacterial aerobic PCB degradation pathway contains 4 steps (bph operon) in which thethird one (bphC) catalyzes the conversion of 2,3-dihydroxybiphenyl into 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid and thus destroyes the biphenyl ring. For this purpose the bphC gene encoding the enzyme 2,3-dihydroxybiphenyl-1,2-dioxygenase was chosen from bacteria Pseudomonas testosteroni B-356 for cloning into plant Nicotiana tabacum. Different constructs in cassette with bphC containing genes for GFP (green fluorescent protein), GUS (glucuronidase) and LUC (luciferase) were prepared to allow sensitive detection of bphC expression in plants. Also construct in which bphC was joined to His tail was designed. The constructs with bphC/GFP was already transformed into the Nicotiana tabacum. The presence of bphC/GFP DNA and RNA was pro

Název v anglickém jazyce

Cloning of bacterial PCB degradative genes to plants

Popis výsledku anglicky

The target of this work is to increase biodegradation of polychlorinated biphenyls (PCBs) by the plants transformed with the gene from bacterial PCB degradation pathway. Bacterial aerobic PCB degradation pathway contains 4 steps (bph operon) in which thethird one (bphC) catalyzes the conversion of 2,3-dihydroxybiphenyl into 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid and thus destroyes the biphenyl ring. For this purpose the bphC gene encoding the enzyme 2,3-dihydroxybiphenyl-1,2-dioxygenase was chosen from bacteria Pseudomonas testosteroni B-356 for cloning into plant Nicotiana tabacum. Different constructs in cassette with bphC containing genes for GFP (green fluorescent protein), GUS (glucuronidase) and LUC (luciferase) were prepared to allow sensitive detection of bphC expression in plants. Also construct in which bphC was joined to His tail was designed. The constructs with bphC/GFP was already transformed into the Nicotiana tabacum. The presence of bphC/GFP DNA and RNA was pro

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

EI - Biotechnologie a bionika

OECD FORD obor

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Projekt

<a href="/cs/project/LN00B030" target="_blank" >LN00B030: Centrum pro molekulární a genovou biotechnologii</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2004

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Int. Biodeterioration and Biodegradation

ISSN

0964-8305

e-ISSN

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Svazek periodika

53

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

1

Strana od-do

247-248

Kód UT WoS článku

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EID výsledku v databázi Scopus

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