Enhanced metabolic flux of methylerythritol phosphate (MEP) pathway by overexpression of Ginkgo biloba 1-Hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate Reductase 1 (GbHDR1) gene in poplar

نویسندگان

چکیده

Abstract Terpenoids are of great interests in a broad range health-beneficial biological activities and various industrial applications. In plants, terpenoids synthesized by two distinct pathways, methylerythritol phosphate (MEP) mevalonate pathways separate location. MEP pathway supplies isoprene precursors isopentenyl diphosphate (IPP) its isomer dimethylallyl (DMAPP) terpenoid biosynthesis plant plastids. The has been an engineering target to increase the metabolic flux towards higher production plants. 1-Hydroxy-2-methyl-2-( E )-butenyl-4-diphosphate reductase (HDR) is terminal step regulate encoded three paralogous genes Ginkgo biloba. this study, we assessed effect overexpression GbHDR1 on metabolism poplar Overexpression plants accelerated growth delayed winter-bud formation. Transcript levels gibberellin, chlorophylls, carotenoid biosynthetic GbHDR1- overexpressing ( ox) poplars were up-regulated, suggesting enhancement. Moreover, enhanced contents chlorophylls carotenoids leaves ox resulted photosynthetic rate as consequence. Therefore, expect will be desirable point for enhancing

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Cloning and analysis of 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase genes HsHDR1 and HsHDR2 in Huperzia serrate

We cloned and analyzed the two genes of the 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase (HDR) gene family from Huperzia serrate. The two transcripts coding HDR, named HsHDR1 and HsHDR2, were discovered in the transcriptome dataset of H. serrate and were cloned by reverse transcription-polymerase chain reaction (RT-PCR). The physicochemical properties, protein domains, protein secon...

متن کامل

Molecular cloning and characterization of 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase (CaHDR) from Camptotheca acuminata and its functional identification in Escherichia coli.

Camptothecin is an anti-cancer monoterpene indole alkaloid. The gene encoding 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase (designated as CaHDR), the last catalytic enzyme of the MEP pathway for terpenoid biosynthesis, was isolated from camptothecin-producing Camptotheca acuminata. The full-length cDNA of CaHDR was 1686 bp encoding 459 amino acids. Comparison of the cDNA and genomic...

متن کامل

Methyl 2 , 5 - Dihydroxy - 4 - ( 3 1 - methyl - 2 1 - butenyl ) benzoate

Methyl 2,5-dihydroxy-4-(31-methyl-21-butenyl)benzoate (1) was isolated from the root of Erythrina subumbrans. The chemical structure of 1 has been elucidated based on spectroscopy UV-Vis, HRESIMS, 1D and 2D NMR analysis.

متن کامل

Isoprenoid biosynthesis via 1-deoxy-D-xylulose 5-phosphate/2-C-methyl-D-erythritol 4-phosphate (DOXP/MEP) pathway.

Higher plants, several algae, bacteria, some strains of Streptomyces and possibly malaria parasite Plasmodium falciparum contain the novel, plastidic DOXP/MEP pathway for isoprenoid biosynthesis. This pathway, alternative with respect to the classical mevalonate pathway, starts with condensation of pyruvate and glyceraldehyde-3-phosphate which yields 1-deoxy-D-xylulose 5-phosphate (DOXP); the l...

متن کامل

Synthesis of 1-Hydroxy-2-(Prop-2'-Enyl) 9-Antrone

An efficient synthesis of the 1-hydroxy-2-(prop-2'-enyl)9-anthrone is described. Selective nitration of anthraquinone, reduction to the corresponding amine, diazotization and treatment by sulfuric acid solution afforded the 1-hydroxy-9,10-anthraquinone in good yield as the key intermediate. Reaction with allyl bromide/K2CO3 and subsequent selective reduction accompanie...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Applied Biological Chemistry

سال: 2022

ISSN: ['2468-0834', '2468-0842']

DOI: https://doi.org/10.1186/s13765-022-00718-6