scholarly journals Biological Stability and Antimicrobial Activity Analysis of Antagonism Actinomycete SC-04 Fermentation Fluid

2016 ◽  
Vol 32 (1) ◽  
pp. 121-126
Author(s):  
Li Wenbin ◽  
Li Zengbo
2019 ◽  
Vol 89 ◽  
pp. 198-206
Author(s):  
Ming Guo ◽  
Huihui Wang ◽  
Yina Shao ◽  
Ronglian Xing ◽  
Xuelin Zhao ◽  
...  

2016 ◽  
Vol 237 ◽  
pp. 1-12 ◽  
Author(s):  
Hongxia Liu ◽  
Xiaoxu Qu ◽  
Ling Gao ◽  
Shengming Zhao ◽  
Zhaoxin Lu ◽  
...  

Toxins ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 514 ◽  
Author(s):  
Hamza Olleik ◽  
Cendrine Nicoletti ◽  
Mickael Lafond ◽  
Elise Courvoisier-Dezord ◽  
Peiwen Xue ◽  
...  

Filamentous fungi, although producing noxious molecules such as mycotoxins, have been used to produce numerous drugs active against human diseases such as paclitaxel, statins, and penicillin, saving millions of human lives. Cyclodepsipeptides are fungal molecules with potentially adverse and positive effects. Although these peptides are not novel, comparative studies of their antimicrobial activity, toxicity, and mechanism of action are still to be identified. In this study, the fungal cyclohexadepsipeptides enniatin (ENN) and beauvericin (BEA) were assessed to determine their antimicrobial activity and cytotoxicity against human cells. Results showed that these peptides were active against Gram-positive bacteria, Mycobacterium, and fungi, but not against Gram-negative bacteria. ENN and BEA had a limited hemolytic effect, yet were found to be toxic at low doses to nucleated human cells. Both peptides also interacted with bacterial lipids, causing low to no membrane permeabilization, but induced membrane depolarization and inhibition of macromolecules synthesis. The structure–activity analysis showed that the chemical nature of the side chains present on ENN and BEA (either iso-propyl, sec-butyl, or phenylmethyl) impacts their interaction with lipids, antimicrobial action, and toxicity.


2021 ◽  
Vol 12 ◽  
Author(s):  
Zhanyi Yang ◽  
Shiqi He ◽  
Hua Wu ◽  
Ting Yin ◽  
Lili Wang ◽  
...  

The security issue of human health is faced with dispiriting threats from multidrug-resistant bacteria infections induced by the abuse and misuse of antibiotics. Over decades, the antimicrobial peptides (AMPs) hold great promise as a viable alternative to treatment with antibiotics due to their peculiar antimicrobial mechanisms of action, broad-spectrum antimicrobial activity, lower drug residue, and ease of synthesis and modification. However, they universally express a series of disadvantages that hinder their potential application in the biomedical field (e.g., low bioavailability, poor protease resistance, and high cytotoxicity) and extremely waste the abundant resources of AMP database discovered over the decades. For all these reasons, the nanostructured antimicrobial peptides (Ns-AMPs), based on a variety of nanosystem modification, have made up for the deficiencies and pushed the development of novel AMP-based antimicrobial therapies. In this review, we provide an overview of the advantages of Ns-AMPs in improving therapeutic efficacy and biological stability, reducing side effects, and gaining the effect of organic targeting and drug controlled release. Then the different material categories of Ns-AMPs are described, including inorganic material nanosystems containing AMPs, organic material nanosystems containing AMPs, and self-assembled AMPs. Additionally, this review focuses on the Ns-AMPs for the effect of biological activities, with emphasis on antimicrobial activity, biosecurity, and biological stability. The “state-of-the-art” antimicrobial modes of Ns-AMPs, including controlled release of AMPs under a specific environment or intrinsic antimicrobial properties of Ns-AMPs, are also explicated. Finally, the perspectives and conclusions of the current research in this field are also summarized.


2020 ◽  
Vol 40 (3) ◽  
pp. 342-348
Author(s):  
Ergül Mutlu ALTUNDAĞ ◽  
Eda BECER ◽  
Gizem ŞANLITÜRK ◽  
Mümtaz GÜRAN ◽  
H. Seda VATANSEVER

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