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海洋放线菌 PNM-161a 菌株来源的环四肽类化合物及其对水稻和山药病原菌的活性

Cyclic tetrapeptides from the marine strain Streptomyces sp. PNM-161a with activity against rice and yam phytopathogens.

机构信息

Universidad Nacional de Colombia, Sede Bogotá, Departamento de Química, Carrera 30 No. 45-03, Edificio de Química of 427, Bogotá, 111321, Colombia.

Universidad de Caldas, Departamento de Química, Edificio Orlando Sierra, Bloque B, Sede Palogrande Calle 65 No. 26-10, Manizales, Caldas, Colombia.

出版信息

J Antibiot (Tokyo). 2019 Oct;72(10):744-751. doi: 10.1038/s41429-019-0201-0. Epub 2019 Jun 26.

Abstract

Two cyclotetrapeptides, henceforth named Provipeptides A (1) and B (2), along with five known diketopiperazines (3-7) were isolated from the liquid culture of marine Streptomyces sp. 161a recovered from a sample of sea grass Bryopsis sp. The structures of cyclotetrapeptides and diketopiperazines (DKPs) were established by 1D and 2D NMR data, MS, and by comparison with literature data. The absolute stereochemistry of compounds cyclo-(L-Pro-L-Leu-D-Pro-L-Phe) 1 and cyclo-(-Pro-Ile-Pro-Phe) 2 was established by the Marfey's method. Compound 1 showed antibacterial activity against rice phytopathogenic strains Burkholderia glumae (MIC = 1.1 mM) and Burkholderia gladioli (MIC = 0.068 mM), compound 2 was active only against B. glumae (MIC = 1.1 mM), and DKP cyclo-[L-Pro-L-Leu] 5 showed to be active against B. gladioli (MIC = 0.3 mM) and B. glumae (MIC = 2.4 mM). Compounds 1 and 2 showed 65% and 50% inhibition of Colletotrichum gloeosporioides (yam pathogen) conidia germination, respectively at a concentration of 1.1 mM.

摘要

从海草 Bryopsis sp. 的样本中回收的海洋链霉菌 sp. 161a 的液体培养物中分离出两种环四肽,分别命名为 Provipeptides A(1)和 B(2),以及五种已知的二酮哌嗪(3-7)。通过 1D 和 2D NMR 数据、MS 以及与文献数据的比较,确定了环四肽和二酮哌嗪(DKP)的结构。通过 Marfey's 方法确定了化合物环-(L-Pro-L-Leu-D-Pro-L-Phe) 1 和环-(-Pro-Ile-Pro-Phe) 2 的绝对立体化学。化合物 1 对稻病原菌菌株 Burkholderia glumae(MIC = 1.1 mM)和 Burkholderia gladioli(MIC = 0.068 mM)表现出抗菌活性,化合物 2 仅对 B. glumae(MIC = 1.1 mM)表现出活性,二酮哌嗪环-[L-Pro-L-Leu] 5 对 B. gladioli(MIC = 0.3 mM)和 B. glumae(MIC = 2.4 mM)表现出活性。化合物 1 和 2 在 1.1 mM 浓度下分别对炭疽病菌(山药病原菌)分生孢子萌发的抑制率分别为 65%和 50%。

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