TY - JOUR
T1 - Total Synthesis and Biological Mode of Action of WAP-8294A2
T2 - A Menaquinone-Targeting Antibiotic
AU - Itoh, Hiroaki
AU - Tokumoto, Kotaro
AU - Kaji, Takuya
AU - Paudel, Atmika
AU - Panthee, Suresh
AU - Hamamoto, Hiroshi
AU - Sekimizu, Kazuhisa
AU - Inoue, Masayuki
N1 - Publisher Copyright:
© Copyright 2017 American Chemical Society.
PY - 2018/7/6
Y1 - 2018/7/6
N2 - WAP-8294A2 (lotilibcin, 1) is a potent antibiotic with superior in vivo efficacy to vancomycin against methicillin-resistant Staphylococcus aureus (MRSA). Despite the great medical importance, its molecular mode of action remains unknown. Here we report the total synthesis of complex macrocyclic peptide 1 comprised of 12 amino acids with a β-hydroxy fatty-acid chain, and its deoxy analogue 2. A full solid-phase synthesis of 1 and 2 enabled their rapid assembly and the first detailed investigation of their functions. Compounds 1 and 2 were equipotent against various strains of Gram-positive bacteria including MRSA. We present evidence that the antimicrobial activities of 1 and 2 are due to lysis of the bacterial membrane, and their membrane-disrupting effects depend on the presence of menaquinone, an essential factor for the bacterial respiratory chain. The established synthetic routes and the menaquinone-targeting mechanisms provide valuable information for designing and developing new antibiotics based on their structures.
AB - WAP-8294A2 (lotilibcin, 1) is a potent antibiotic with superior in vivo efficacy to vancomycin against methicillin-resistant Staphylococcus aureus (MRSA). Despite the great medical importance, its molecular mode of action remains unknown. Here we report the total synthesis of complex macrocyclic peptide 1 comprised of 12 amino acids with a β-hydroxy fatty-acid chain, and its deoxy analogue 2. A full solid-phase synthesis of 1 and 2 enabled their rapid assembly and the first detailed investigation of their functions. Compounds 1 and 2 were equipotent against various strains of Gram-positive bacteria including MRSA. We present evidence that the antimicrobial activities of 1 and 2 are due to lysis of the bacterial membrane, and their membrane-disrupting effects depend on the presence of menaquinone, an essential factor for the bacterial respiratory chain. The established synthetic routes and the menaquinone-targeting mechanisms provide valuable information for designing and developing new antibiotics based on their structures.
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U2 - 10.1021/acs.joc.7b02318
DO - 10.1021/acs.joc.7b02318
M3 - Article
C2 - 29019678
AN - SCOPUS:85049623240
SN - 0022-3263
VL - 83
SP - 6924
EP - 6935
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 13
ER -