Enhancement of neomycin production by engineering the entire biosynthetic gene cluster and feeding key precursors in Streptomyces fradiae CGMCC 4.576

2019 ◽  
Vol 103 (5) ◽  
pp. 2263-2275 ◽  
Author(s):  
Jiazhen Zheng ◽  
Yue Li ◽  
Hanye Guan ◽  
Jihui Zhang ◽  
Huarong Tan
2005 ◽  
Vol 33 (2) ◽  
pp. 129-140 ◽  
Author(s):  
Vivian Miao ◽  
Renee Brost ◽  
Joanne Chapple ◽  
Kevin She ◽  
Marie-François Coëffet-Le Gal ◽  
...  

2005 ◽  
Vol 3 (8) ◽  
pp. 1410 ◽  
Author(s):  
Fanglu Huang ◽  
Stephen F. Haydock ◽  
Tatiana Mironenko ◽  
Dieter Spiteller ◽  
Yanyan Li ◽  
...  

Author(s):  
Joana Martins ◽  
Niina Leikoski ◽  
Matti Wahlsten ◽  
Joana Azevedo ◽  
Jorge Antunes ◽  
...  

Cyanobactins are a family of linear and cyclic peptides produced through the post-translational modification of short precursor peptides. Anacyclamides are macrocyclic cyanobactins with a highly diverse sequence that are common in the genus <i>Anabaena</i>. A mass spectrometry-based screening of potential cyanobactin producers led to the discovery of a new prenylated member of this family of compounds, anacyclamide D8P (<b>1</b>), from <i>Sphaerospermopsis</i> sp. LEGE 00249. The anacyclamide biosynthetic gene cluster (<i>acy</i>) encoding the novel macrocyclic prenylated cyanobactin, was sequenced. Heterologous expression of the acy gene cluster in <i>Escherichia</i> <i>coli</i> established the connection between genomic and mass spectrometric data. Unambiguous establishment of the type and site of prenylation required the full structural elucidation of <b>1</b> using Nuclear Magnetic Resonance (NMR), which demonstrated that a forward prenylation occurred on the tyrosine residue. Compound <b>1</b> was tested in pharmacologically or ecologically relevant biological assays and revealed moderate antimicrobial activity towards the fouling bacterium <i>Halomonas aquamarina</i> CECT 5000.<br>


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