Halogenated compound secreted by marine bacteria halts larval urchin development

2021 ◽  
Vol 538 ◽  
pp. 151540
Author(s):  
S.M.K. Akkipeddi ◽  
M. Xu ◽  
K.Y.K. Chan
Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
V Guillemard ◽  
L Guentas-Dombrowsky ◽  
E Lobbens ◽  
C Payri

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
C Roullier ◽  
Y Guitton ◽  
S Prado ◽  
O Grovel ◽  
YF Pouchus

Author(s):  
Adyasa Barik ◽  
Pandiyan Rajesh ◽  
Manthiram Malathi ◽  
Vellaisamy Balasubramanian

: In recent years, over use of antibiotics has been raising its head to a serious problem all around the world as pathogens become drug resistant and create challenges to the medical field. This failure of most potent antibiotics that kill pathogens increases the thirst for research to look further way of killing pathogens. It has been led to the findings of antimicrobial peptide which is the most potent peptide to destroy pathogens. This review gives special emphasis to the usage of marine bacteria and other microorganisms for antimicrobial peptide (AMP) which are eco friendly as well as a developing class of natural and synthetic peptides with a wide spectrum of targets to pathogenic microbes. Consequently, a significant attention has been paid mainly to (i) the structure and types of anti microbial peptides and (ii) mode of action and mechanism of antimicrobial peptide resistance to pathogens. In addition to this, the designing of AMPs has been analysed thoroughly for reducing toxicity and developing better potent AMP. It has been done by the modified unnatural amino acids by amidation to target the control of biofilm and persister cell.


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