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Synthesis, characterization, and antibacterial property of novel starch derivatives with 1,2,3-triazole

机译:1,2,3-三唑类新型淀粉衍生物的合成,表征及抗菌性能

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摘要

Four novel starch-linked-1,2,3-triazole derivatives were synthesized including 6-hydroxymethyltriazole6-deoxy starch (HMTST), 6-bromomethyltriazole-6-deoxy starch (BMTST), 6-chloromethyltriazole-6-deoxy starch (CMTST), and 6-carboxyltriazole-6-deoxy starch (CBTST). Their antibacterial properties against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were evaluated in vitro, respectively. The inhibitory property of the obtained amphiprotic starch derivatives exhibited a remarkable improvement over starch. And the antibacterial indices of most of the products were higher than 60% and 40% at 1.0 mg/mL when the culture time was 8 h and 16 h, respectively. Moreover, the inhibitory index of CBTST attained 97% above at 1.0 mg/mL. Generally, the inhibitory activity decreased in the order: CBTST > CMTST > BMTST > HMTST> starch. Furthermore, the order of their antibacterial activity was consistent with the electron-withdrawing property of different substituted groups of the 1,2,3-triazole groups. The substituted groups with stronger electron withdrawing ability relatively possessed greater antibacterial activity. (C) 2016 Elsevier Ltd. All rights reserved.
机译:合成了四种新颖的淀粉连接的1,2,3-三唑衍生物,包括6-羟甲基三唑6-脱氧淀粉(HMTST),6-溴甲基三唑-6-脱氧淀粉(BMTST),6-氯甲基三唑-6-脱氧淀粉(CMTST) ,6-羧基三唑-6-脱氧淀粉(CBTST)。分别评估了它们对大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)的抗菌性能。所获得的两性淀粉衍生物的抑制性能比淀粉显示出显着的改善。当培养时间分别为8 h和16 h时,大多数产品的抗菌指数在1.0 mg / mL时分别高于60%和40%。而且,在1.0mg / mL下,CBTST的抑制指数达到97%以上。通常,抑制活性的顺序为:CBTST> CMTST> BMTST> HMTST>淀粉。此外,它们的抗菌活性的顺序与1,2,3-三唑基的不同取代基的吸电子性能一致。具有更强吸电子能力的取代基相对具有更大的抗菌活性。 (C)2016 Elsevier Ltd.保留所有权利。

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