Role of cytochrome P450 1A2 and N-acetyltransferase 2 in 2, 6-dimethylaniline induced genotoxicity

Abstract The purpose of the current work was to assess a possible role of cytochrome P450 1A2 (CYP1A2) and N-acetyltransferase 2 (NAT2) in the metabolic activation of 2,6-dimethylaniline (2,6-DMA) and also clarify the function of DNA repair in affecting the ultimate mutagenic potency. Two cell lines, nucleotide excision repair (NER)-deficient 5P3NAT2 and proficient 5P3NAT2R9 both expressing CYP1A2 and NAT2, were treated with 2,6-DMA for 48 h or its metabolites for 1 h. Cell survival determined by trypan blue exclusion and MTT assays, and 8-azaadenine-resistant mutants at the adenine phosphoribosyltransferase (aprt) gene locus were evaluated. 5P3NAT2 and 5P3NAT2R9 cells treated with 2,6-DMA and its metabolites showed a dose-dependent increase in cytotoxicity and mutant fraction; N-OH-2,6-DMA and 2,6-DMAP in serum-free α-minimal essential medium (MEM) are more potent than 2,6-DMA in complete MEM. 5P3NAT2 cells was more sensitive to the cytotoxic and mutagenic action than 5P3NAT2R9 cells. H2DCFH-DA assay showed dose-dependent ROS production under 2,6- DMAP treatment. These findings indicate that the genotoxic effects of 2,6-DMA are mediated by CYP1A2 activation via N-hydroxylation and the subsequent esterification by the phase II conjugation enzyme NAT2, and through the generation of ROS by hydroxylamine and/or aminophenol metabolites. NER status is also an important contributor

The effect of inhibitors on photosynthetic electron transport chain in canola leaf discs / Efeito de inibidores na cadeia de transporte de elétrons fotossintética em discos foliares de canola

The mechanisms of photosynthetic electron transport can be elucidated by inhibition of electron flow through the use of specific substances that, when combined with the chlorophyll chlorophyll a fluorescence emission was measured to investigate the effect of several inhibitors of the photosynthetic electron transport chain in canola leaf discs. Leaf discs were incubated in the dark for 2 hours in different solutions: (a) water ­ control; (b) DCMU at 500 µM; (c) phenanthroline at 10 mM; and (d) hydroxylamine at 10, 50, 100 and 200 mM. Similar effects were observed between DCMU and phenanthroline, the initial fluorescence value was altered, but not the maximum fluorescence, with the disappearance of the IP phase. Hydroxylamine interacted and inhibited the oxygen evolving complex and caused an imbalance between the rate of QA reduction by photosystem II and the rate of QA oxidation by photosystem I.

Os mecanismos de transporte de elétrons podem ser elucidados pela inibição do fluxo de elétrons pelo uso de substâncias específicas que, juntamente com a técnica de fluorescência da clorofila, torna-se uma ferramenta importante para detalhar a cadeia de transporte de elétrons. Neste trabalho, a emissão da fluorescência da clorofila foi mensurada para investigar o efeito dos diferentes inibidores da cadeia de transporte de elétrons fotossintéticos de discos foliares de canola. Os discos foliares foram incubados no escuro durante 02 h em diferentes soluções: (a) água - controle, (b) 500 uM de DCMU, (c) 10 mM de fenantrolina, e (d) 10, 50, 100 e 200 mM de hidroxilamina. Foram observados efeitos similares entre DCMU e fenantrolina, o valor da fluorescência inicial foi alterado, contudo a fluorescência máxima não se alterou, havendo o desaparecimento da fase de IP. Hidroxilamina interagiu e inibiu o complexo de evolução de oxigênio e causou desequilíbrio entre a taxa de redução QA pelo fotossistema II e a taxa de oxidação QA pelo fotossistema I.

Construction of expression vectors for efficient expression of soluble recombinant proteins / 生物工程学报

The aim of the study is to construct two vectors for efficient expression of soluble recombinant proteins. The first vector was constructed by cloning the HisSUMO fragment into an expression vector pET30a(+) to fuse with the gene of interest (designated as HisSUMO Express). The second vector was constructed in the same way, but with a hydroxylamine cleavage site between HisSUMO and the gene of interest for an economic purpose (designated as HisSUMO Economic). The mouse fibroblast growth factor-21(mFGF-21), which was difficult to express in routine-used expression vectors, was taken as an example to test the vectors. The results showed that the mFGF-21 was expressed at high level in both vectors. The Sumo/mFGF-21 fusion protein accounted for more than 40% of the total bacterial protein. The fusion protein was purified with Ni-TNA column, and the HisSUMO was removed by cleavage of the fusion protein with either hydroxylamine solution or SUMO protease I. The concentration of the purified mFGF-21 mature protein was 54 mg/L and the recovery rate was 6%. The purified proteins derived from either hydroxylamine or SUMO protease I cleavage could stimulate glucose up-take by adipocytes. These results indicated that both HisSUMO Express and HisSUMO Economic were useful expression vectors for efficient expression of soluble recombinant proteins.

N-galloylhydroxylamine from pentagalloylglucose: analgesic and anti-inflammatory activities, semi-synthesis

The pericarp of Harpullia pendula, 1, 2, 3, 4, 6-penta-O-galloyl-beta-D-glucopyranose, as a major gallotannin [7], was isolated together with other six polyphenolic metabolites. Their structures were established as gallic acid [1], methylgallate [2], ethylgallate [3], chlorogenic acid [4], 1, 2, 6-tri-O-galloyl-beta-D-glucopyranose [5] 1, 2, 4, 6-teta-O-galloyl-beta-Dglucopyranose [6], according the chromatographic properties, chemical and spectroscopic analyses. Compound 7 was subjected to a semi-synthesis with hydroxylamine hydrochloride resulting in a significant analgesic and anti-inflammatory N-galloyl-hydroxylamine bioactive product [8], which exhibited at dose [100 mg/kg] high significant analgesic and anti-inflammatory activities compared with indomethacin in dose [10 mg/kg]

Synthesis and reactions of B-ketoanilides for biological evaluation

2-Arylidene cycloalkanones react with acetocetanilide to give the corresponding B-ketoanilides Ia-f which react with hydroxyl-amine and/or hydrazine hydrate in acetic acid to give respectively compounds III and compounds V. Compounds I also react with o-phenylene diamine and/or diethyl malonatethiourea to produce respectively compounds VI and compounds VIII. Chemical screening for the products are mentioned

Use of hydroxylamine in improving radio protection of a combination of 5-hydroxy L-tryptophan and a thiol compound (AET) in small mammals.

Radioprotective effectiveness has been evaluated by 30 day survival studies and protection to bone-marrow cells in mice after radiation exposure and this has been further established by 24 hr deoxycytidine excretion in urine of rats following 5 Gy whole body gamma irradiation and protection to superoxide dismutase enzyme in marrow cells and red blood corpuscles. Radioprotective effectiveness as well as the duration of radioprotection have been improved by the administration (ip) of hydroxylamine (20 mg/kg), a decarboxylase inhibitor, prior to the use of a combination of 5-hydroxy L-tryptophan (5-HTP, 70 mg/kg) and 2-aminoethylisothiuronium bromide hydrobromide (AET, 20 mg/kg) ip in small mammals before whole body gamma irradiation.