Klonování bakteriálních PCB degradujícícg genů do rostliny Nicotina tabacum

Kód výsledku v IS VaVaI

RIV/60461373:22330/04:00012750 - isvavai.cz

Výsledek na webu

—

DOI - Digital Object Identifier

—

Jazyk výsledku

angličtina

Název v původním jazyce

Cloning of a bacterial PCB-degrading gene into the plants of Nicotiana tabacum

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 a bacterial PCB-degrading gene into the plants of Nicotiana tabacum

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

D - Stať ve sborníku

CEP obor

DK - Kontaminace a dekontaminace půdy včetně pesticidů

OECD FORD obor

—

Projekt

LN00B030: Centrum pro molekulární a genovou biotechnologii

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 statě ve sborníku

Proceeding of the 6th International Symposium and Exhibition on Environmental Contamination in Central and eastern Europe

ISBN

0-9748192-0-4

ISSN

—

e-ISSN

—

Počet stran výsledku

1

Strana od-do

479

Název nakladatele

Florida State University

Místo vydání

Florida

Místo konání akce

Praha

Datum konání akce

1. 9. 2004

Typ akce podle státní příslušnosti

WRD - Celosvětová akce

Kód UT WoS článku

—