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1.
Arch Insect Biochem Physiol ; 91(1): 17-36, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26440910

RESUMO

The insect peptide hormone trypsin modulating oostatic factor (TMOF), a decapeptide that is synthesized by the mosquito ovary and controls the translation of the gut's trypsin mRNA was cloned and expressed in the marine alga Chlorella desiccata. To express Aedes aegypti TMOF gene (tmfA) in C. desiccata cells, two plasmids (pYES2/TMOF and pYDB4-tmfA) were engineered with pKYLX71 DNA (5 Kb) carrying the cauliflower mosaic virus (CaMV) promoter 35S(2) and the kanamycin resistant gene (neo), as well as, a 8 Kb nitrate reductase gene (nit) from Chlorella vulgaris. Transforming C. desiccata with pYES2/TMOF and pYDB4-tmfA show that the engineered algal cells express TMOF (20 ± 4 µg ± SEM and 17 ± 3 µg ± SEM, respectively in 3 × 10(8) cells) and feeding the cells to mosquito larvae kill 75 and 60% of Ae. aegypti larvae in 4 days, respectively. Southern and Northern blots analyses show that tmfA integrated into the genome of C. desiccata by homologous recombination using the yeast 2 µ circle of replication and the nit in pYES2/TMOF and pYDB4-tmfA, respectively, and the transformed algal cells express tmfA transcript. Using these algal cells it will be possible in the future to control mosquito larvae in the marsh.


Assuntos
Aedes/genética , Chlorella/genética , Hormônios de Inseto/genética , Proteínas de Insetos/genética , Hormônios Peptídicos/genética , Controle Biológico de Vetores/métodos , Aedes/crescimento & desenvolvimento , Aedes/metabolismo , Animais , Chlorella/metabolismo , Clonagem Molecular , Hormônios de Inseto/metabolismo , Proteínas de Insetos/metabolismo , Larva/genética , Larva/crescimento & desenvolvimento , Larva/metabolismo , Organismos Geneticamente Modificados/genética , Organismos Geneticamente Modificados/metabolismo , Hormônios Peptídicos/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo
2.
J Exp Bot ; 66(13): 3725-35, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25922486

RESUMO

Triglycerides (TAGs) from microalgae can be utilized as food supplements and for biodiesel production, but little is known about the regulation of their biosynthesis. This work aimed to test the relationship between acetyl-CoA (Ac-CoA) levels and TAG biosynthesis in green algae under nitrogen deprivation. A novel, highly sensitive liquid chromatography mass spectrometry (LC-MS/MS) technique enabled us to determine the levels of Ac-CoA, malonyl-CoA, and unacetylated (free) CoA in green microalgae. A comparative study of three algal species that differ in TAG accumulation levels shows that during N starvation, Ac-CoA levels rapidly rise, preceding TAG accumulation in all tested species. The levels of Ac-CoA in the high TAG accumulator Chlorella desiccata exceed the levels in the moderate TAG accumulators Dunaliella tertiolecta and Chlamydomonas reinhardtii. Similarly, malonyl-CoA and free CoA levels also increase, but to lower extents. Calculated cellular concentrations of Ac-CoA are far lower than reported K mAc-CoA values of plastidic Ac-CoA carboxylase (ptACCase) in plants. Transcript level analysis of plastidic pyruvate dehydrogenase (ptPDH), the major chloroplastic Ac-CoA producer, revealed rapid induction in parallel with Ac-CoA accumulation in C. desiccata, but not in D. tertiolecta or C. reinhardtii. It is proposed that the capacity to accumulate high TAG levels in green algae critically depends on their ability to divert carbon flow towards Ac-CoA. This requires elevation of the chloroplastic CoA pool level and enhancement of Ac-CoA biosynthesis. These conclusions may have important implications for future genetic manipulation to enhance TAG biosynthesis in green algae.


Assuntos
Acetilcoenzima A/biossíntese , Chlorella/metabolismo , Triglicerídeos/metabolismo , Acetil-CoA Carboxilase/metabolismo , Sequência de Aminoácidos , Chlorella/efeitos dos fármacos , Chlorella/crescimento & desenvolvimento , Coenzima A/metabolismo , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Malonil Coenzima A/metabolismo , Redes e Vias Metabólicas/efeitos dos fármacos , Dados de Sequência Molecular , Nitrogênio/farmacologia , Proteínas de Plantas/química , Proteínas de Plantas/metabolismo , Plastídeos/efeitos dos fármacos , Plastídeos/enzimologia , Piruvato Desidrogenase (Lipoamida)/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Padrões de Referência , Amido/metabolismo
3.
J Exp Bot ; 66(22): 7287-98, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26357883

RESUMO

In a recent study, it has been shown that biosynthesis of triacylglycerol (TAG) in the oleaginous green alga Chlorella desiccata is preceded by a large increase in acetyl-coenzyme A (Ac-CoA) levels and by upregulation of plastidic pyruvate dehydrogenase (ptPDH). It was proposed that the capacity to accumulate high TAG critically depends on enhanced production of Ac-CoA. In this study, two alternative Ac-CoA producers-plastidic Ac-CoA synthase (ptACS) and ATP citrate lyase (ACL)-are shown to be upregulated prior to TAG accumulation under nitrogen deprivation in the oleaginous species C. desiccata, but not in the moderate TAG accumulators Dunaliella tertiolecta and Chlamydomonas reinhardtii. Measurements of endogenous acetate production and of radiolabelled acetate incorporation into lipids are consistent with the upregulation of ptACS, but suggest that its contribution to the overall TAG biosynthesis is negligible. Induction of ACS and production of endogenous acetate are correlated with activation of alcohol dehydrogenase, suggesting that the upregulation of ptACS is associated with activation of PDH-bypass in C. desiccata. It is proposed that activation of the PDH-bypass in C. desiccata is needed to enable a high rate of lipid biosynthesis under nitrogen deprivation by controlling the level of pyruvate reaching ptPHD and/or mtPDH. This may be an important parameter for massive TAG accumulation in microalgae.


Assuntos
Acetato-CoA Ligase/metabolismo , Chlorella/enzimologia , Complexo Piruvato Desidrogenase/metabolismo , ATP Citrato (pro-S)-Liase/metabolismo , Álcool Desidrogenase/metabolismo , Ativação Enzimática , Nitrogênio/metabolismo , Oxigênio/metabolismo , Plastídeos/enzimologia , Triglicerídeos/metabolismo
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