Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros

Bases de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
ACS Chem Biol ; 19(5): 1169-1179, 2024 05 17.
Artículo en Inglés | MEDLINE | ID: mdl-38624108

RESUMEN

Bufadienolides are a class of steroids with a distinctive α-pyrone ring at C17, mostly produced by toads and consisting of over 100 orthologues. They exhibit potent cardiotonic and antitumor activities and are active ingredients of the traditional Chinese medicine Chansu and Cinobufacini. Direct extraction from toads is costly, and chemical synthesis is difficult, limiting the accessibility of active bufadienolides with diverse modifications and trace content. In this work, based on the transcriptome and genome analyses, using a yeast-based screening platform, we obtained eight cytochrome P450 (CYP) enzymes from toads, which catalyze the hydroxylation of bufalin and resibufogenin at different sites. Moreover, a reported fungal CYP enzyme Sth10 was found functioning in the modification of bufalin and resibufogenin at multiple sites. A total of 15 bufadienolides were produced and structurally identified, of which six were first discovered. All of the compounds were effective in inhibiting the proliferation of tumor cells, especially 19-hydroxy-bufalin (2) and 1ß-hydroxy-bufalin (3), which were generated from bufalin hydroxylation catalyzed by CYP46A35. The catalytic efficiency of CYP46A35 was improved about six times and its substrate diversity was expanded to progesterone and testosterone, the common precursors for steroid drugs, achieving their efficient and site-specific hydroxylation. These findings elucidate the key modification process in the synthesis of bufadienolides by toads and provide an effective way for the synthesis of unavailable bufadienolides with site-specific modification and active potentials.


Asunto(s)
Bufanólidos , Sistema Enzimático del Citocromo P-450 , Bufanólidos/química , Bufanólidos/metabolismo , Bufanólidos/farmacología , Sistema Enzimático del Citocromo P-450/metabolismo , Animales , Humanos , Antineoplásicos/farmacología , Antineoplásicos/química , Antineoplásicos/metabolismo , Hidroxilación , Línea Celular Tumoral , Bufonidae/metabolismo , Proliferación Celular/efectos de los fármacos
2.
Sheng Wu Gong Cheng Xue Bao ; 37(10): 3622-3635, 2021 Oct 25.
Artículo en Chino | MEDLINE | ID: mdl-34708615

RESUMEN

Bioremediation is considered as a cost-effective, efficient and free-of-secondary-pollution technology for petroleum pollution remediation. Due to the limitation of soil environmental conditions and the nature of petroleum pollutants, the insufficient number and the low growth rate of indigenous petroleum-degrading microorganisms in soil lead to long remediation cycle and poor remediation efficiency. Bioaugmentation can effectively improve the biodegradation efficiency. By supplying functional microbes or microbial consortia, immobilized microbes, surfactants and growth substrates, the remediation effect of indigenous microorganisms on petroleum pollutants in soil can be boosted. This article summarizes the reported petroleum-degrading microbes and the main factors influencing microbial remediation of petroleum contaminated soil. Moreover, this article discusses a variety of effective strategies to enhance the bioremediation efficiency, as well as future directions of bioaugmentation strategies.


Asunto(s)
Petróleo , Contaminantes del Suelo , Biodegradación Ambiental , Suelo , Microbiología del Suelo
3.
J Hazard Mater ; 385: 121616, 2020 03 05.
Artículo en Inglés | MEDLINE | ID: mdl-31780289

RESUMEN

The efficient bioremediation of estrogen contamination in complex environments is of great concern. Here the strain Stenotrophomonas maltophilia SJTH1 was found with great and stable estrogen-degradation efficiency even under stress environments. The strain could utilize 17ß-estradiol (E2) as a carbon source and degrade 90% of 10 mg/L E2 in a week; estrone (E1) was the first degrading intermediate of E2. Notably, diverse pH conditions (3.0-11.0) and supplements of 4% salinity, 6.25 mg/L of heavy metal (Cd2+ or Cu2+), or 1 CMC of surfactant (Tween 80/ Triton X-100) had little effect on its cell growth and estrogen degradation. The addition of low concentrations of copper and Tween 80 even promoted its E2 degradation. Bioaugmentation of strain SJTH1 into solid clay soil achieved over 80% removal of E2 contamination (10 mg/kg) within two weeks. Further, the whole genome sequence of S. maltophilia SJTH1 was obtained, and a series of potential genes participating in stress-tolerance and estrogen-degradation were predicted. Four dehydrogenases similar to 17ß-hydroxysteroid dehydrogenases (17ß-HSDs) were found to be induced by E2, and the four heterogenous-expressed enzymes could oxidize E2 into E1 efficiently. This work could promote bioremediation appliance potential with microorganisms and biodegradation mechanism study of estrogens in complex real environments.


Asunto(s)
Proteínas Bacterianas/aislamiento & purificación , Estradiol Deshidrogenasas/aislamiento & purificación , Estradiol/metabolismo , Stenotrophomonas maltophilia/metabolismo , Secuencia de Aminoácidos , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Biodegradación Ambiental , Estradiol Deshidrogenasas/química , Estradiol Deshidrogenasas/genética , Cinética , Octoxinol/farmacología , Oxidación-Reducción , Polisorbatos/farmacología , Alineación de Secuencia , Stenotrophomonas maltophilia/efectos de los fármacos , Stenotrophomonas maltophilia/enzimología , Stenotrophomonas maltophilia/genética , Tensoactivos/farmacología
4.
J Asian Nat Prod Res ; 15(1): 89-93, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23324033

RESUMEN

Aglinin A (1) is a mixture of C(24)-epimeric 20S,24-epoxy-24,25-dihydroxy-3,4-secodammar-4(28)-en-3-oic acid and present in plants of the family Meliaceae. The two epimers of 1 were resolved through an acetonide reaction, and the absolute configurations of two derivatives were deduced by the analysis of their (13)C NMR differences induced by γ-gauche or steric effect. Based on it, the (13)C NMR assignment of 24R-1 and 24S-1 was also established.


Asunto(s)
Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/aislamiento & purificación , Meliaceae/química , Triterpenos/química , Triterpenos/aislamiento & purificación , Medicamentos Herbarios Chinos/farmacología , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Estereoisomerismo , Triterpenos/farmacología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA