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1.
Materials (Basel) ; 12(6)2019 Mar 21.
Artigo em Inglês | MEDLINE | ID: mdl-30901888

RESUMO

DNA nanostructures, owing to their controllable and adaptable nature, have been considered as highly attractive nanoplatforms for biomedical applications in recent years. However, their use in the biological environment has been restricted by low cellular transfection efficiency in mammalian cells, weak stability under physiological conditions, and endonuclease degradation. Herein, we demonstrate an effective approach to facilitate fast transfection of DNA nanostructures and enhance their stability by encapsulating DNA origami with a biocompatible cationic protein (cHSA) via electrostatic interaction. The coated DNA origami is found to be stable under physiological conditions. Moreover, the cHSA coating could significantly improve the cellular transfection efficiency of DNA origami, which is essential for biological applications.

2.
Nat Prod Res ; 31(4): 404-410, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-27050657

RESUMO

Two new pimarane-type diterpenes, scopararanes H-I (1-2), along with five known ones (3-7) were isolated from the culture broth of a marine sediment-derived fungus Eutypella sp. FS46, which was obtained from the South China Sea. Their structures were established by extensive spectroscopic analysis. All of them were evaluated for their cytotoxic activities against MCF-7, NCI-H460 and SF-268 tumour cell lines. Scopararane I (2) showed moderate inhibitory activities.


Assuntos
Abietanos/isolamento & purificação , Antineoplásicos/isolamento & purificação , Sedimentos Geológicos/microbiologia , Xylariales/metabolismo , Abietanos/química , Abietanos/farmacologia , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Fermentação , Humanos
3.
J Asian Nat Prod Res ; 19(2): 145-151, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-27256790

RESUMO

Eutypellol A (1), the first norsesquiterpenoid of sequicarene family, as well as eutypellol B (2), a rare 7-methyl oxidized 2-carene derivative, and one new natural product 2-(2-hydroxy-4-methylcyclohex-3-enyl)propanoic acid (3), along with eight known terpenoids, were isolated from the marine sediment-derived fungus Eutypella scoparia FS46 collected from the South China Sea. Their structures were established on the basis of extensive spectroscopic analysis. Compounds 1-3 were evaluated for their antibacterial activities against Staphylococcus aureus and cytotoxic activities against MCF-7, NCI-H460, and SF-268 tumor cell lines.


Assuntos
Antibacterianos/isolamento & purificação , Monoterpenos/isolamento & purificação , Sesquiterpenos/isolamento & purificação , Antibacterianos/química , Antibacterianos/farmacologia , Ensaios de Seleção de Medicamentos Antitumorais , Sedimentos Geológicos , Humanos , Biologia Marinha , Testes de Sensibilidade Microbiana , Estrutura Molecular , Monoterpenos/química , Monoterpenos/farmacologia , Sesquiterpenos/química , Sesquiterpenos/farmacologia , Staphylococcus aureus/efeitos dos fármacos
4.
J Ind Microbiol Biotechnol ; 43(5): 641-50, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26803504

RESUMO

Epothilone B has drawn great attention due to its much stronger anticancer activity and weaker side effects compared with taxol. The relative low yield of epothilone B limited its application. In this study, we report the successful introduction of the vgb gene and the epoF gene into Sorangium cellulosum So ce M4 by electroporation for the first time, which was demonstrated by Southern blot analysis. Results of qRT-PCR, SDS-PAGE and western blot analysis confirmed the transcription and expression of the vgb and epoF genes. LC-MS results showed that the epothilones B, A yields were improved and epothilones D, C yields were decreased. The yields of epothilone B were improved by 57.9 ± 0.3, 62.7 ± 0.8 and 122.4 ± 0.7 % through the introduction of vgb gene, epoF gene and both genes into strain So ce M4, respectively. Our study provides a new approach for improving epothilone B yield in S. cellulosum.


Assuntos
Epotilonas/biossíntese , Hemoglobinas/genética , Engenharia Metabólica , Myxococcales/genética , Myxococcales/metabolismo , Oxirredutases/genética , Transgenes/genética , Eletroporação , Epotilonas/análise , Vitreoscilla/genética
5.
Molecules ; 20(12): 22900-7, 2015 Dec 21.
Artigo em Inglês | MEDLINE | ID: mdl-26703548

RESUMO

Four new meroterpenoids, guignardones P-S (1-4), and three known analogues (5-7) were isolated from the endophytic fungal strain Guignardia mangiferae A348. Their structures were elucidated on the basis of spectroscopic analysis and single crystal X-ray diffraction. All the isolated compounds were evaluated for their inhibitory effects on SF-268, MCF-7, and NCI-H460 human cancer cell lines. Compounds 2 and 4 exhibited weak inhibitions of cell proliferation against MCF-7 cell line.


Assuntos
Ascomicetos/química , Mangifera/química , Plantas Medicinais/microbiologia , Smilax/microbiologia , Terpenos/química , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Cristalografia por Raios X/métodos , Humanos , Células MCF-7 , Plantas Medicinais/química , Smilax/química , Terpenos/farmacologia , Difração de Raios X/métodos
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