The milbemycins are a group of macrolides chemically related to the avermectins and were first isolated in 1972 from Streptomyces hygroscopicus. They are used in veterinary medicine as antiparasitic agents against worms, ticks and fleas.[1]
Mechanism of action
editMilbemycins have a similar mechanism of action, but a longer half-life than the avermectins. They open glutamate-sensitive chloride channels in neurons and myocytes of invertebrates, leading to hyperpolarisation of these cells and blocking of signal transfer.[citation needed]
Milbemycin is effective against some avermectin-resistant insects.[2]
Biosynthesis
editLike avermectins, milbemycins are products of fermentation by Streptomyces species. A grand total of five species, namely S. hygroscopicus, S. griseochromogenes, S. cyaneogriseus, S. nanchanggensis and S. bingchenggensis, are known to produce this family of compounds.[2]
The biosynthetic cluster from S. bingchenggensis and S. nanchanggensis have been sequenced and analyzed, partly by analogy to the homologous biosynthetic cluster for avermectin. New regulatory elements that control how much milbemycins are being identified in hopes to improve the industrial fermentation yield of milbemycins, which (as of 2021) is much lower than that of avermectin.[2]
An alternative pathway to higher yields was demonstrated in 2017, when select genes from S. avermitilis were swapped out so the avermectin producer makes milbemycin instead.[2]
Examples
edit
| Name | =R1 | =R2 | –R3 |
|---|---|---|---|
| Milbemectin | –H, (β)–OH | –H, –H | –CH3 : –CH2CH3 = 3:7 |
| Milbemycin oxime | =NOH | –H, –H | –CH3 : –CH2CH3 = 3:7 |
| Moxidectin | –H, (β)–OH | =NOCH3 | (Z)–C(CH3)=CH–CH(CH3)2[1] |
| Nemadectin | –H, (β)–OH | –H, (α)–OH | (Z)–C(CH3)=CH–CH(CH3)2[1] |
References
edit- ^ a b c The 2nd International Electronic Conference on Synthetic Organic Chemistry: Insecticides Archived 2008-04-18 at the Wayback Machine
- ^ a b c d Yan, YS; Xia, HY (December 2021). "Recent advances in the research of milbemycin biosynthesis and regulation as well as strategies for strain improvement". Archives of Microbiology. 203 (10): 5849–5857. doi:10.1007/s00203-021-02575-1. PMID 34550409. S2CID 237594779.
 | This antiinfective drug article is a stub. You can help Wikipedia by expanding it. |