pyranonigrin G 在
Saccharomyces cerevisiae SCKW12 transformed with pKW20221 plasmides expressing pynB domain of protein from Aspergillus niger A1179 strain 作用下,
以
水 为溶剂,
反应 4.0h,
生成 pyranonigrin E
参考文献:
名称:
Elucidation of Pyranonigrin Biosynthetic Pathway Reveals a Mode of Tetramic Acid, Fused γ-Pyrone, and exo-Methylene Formation
摘要:
Successful activation of the pyranonigrin biosynthetic gene cluster and gene knockout in Aspergillus niger plus in vivo and in vitro assays led to isolation of six new products, including a spiro cydobutane-containing dimeric compound, which served as the basis for the proposed comprehensive pyranonigrin biosynthetic pathway. Two redox enzymes are key to forming the characteristic fused gamma-pyrone core, and a protease homologue performs the exo-methylene formation.
DOI:
10.1021/acs.orglett.5b02435
作为产物:
描述:
pyranonigrin E 在
nicotinamide adenine dinucleotide phosphate 、 recombinant PynE domain of protein from Aspergillus niger A1179 strain 、 三羟甲基氨基甲烷盐酸盐 、 sodium chloride 作用下,
以
水 为溶剂,
反应 1.0h,
生成 pyranonigrin G
参考文献:
名称:
Elucidation of Pyranonigrin Biosynthetic Pathway Reveals a Mode of Tetramic Acid, Fused γ-Pyrone, and exo-Methylene Formation
摘要:
Successful activation of the pyranonigrin biosynthetic gene cluster and gene knockout in Aspergillus niger plus in vivo and in vitro assays led to isolation of six new products, including a spiro cydobutane-containing dimeric compound, which served as the basis for the proposed comprehensive pyranonigrin biosynthetic pathway. Two redox enzymes are key to forming the characteristic fused gamma-pyrone core, and a protease homologue performs the exo-methylene formation.
Successful activation of the pyranonigrin biosynthetic gene cluster and gene knockout in Aspergillus niger plus in vivo and in vitro assays led to isolation of six new products, including a spiro cydobutane-containing dimeric compound, which served as the basis for the proposed comprehensive pyranonigrin biosynthetic pathway. Two redox enzymes are key to forming the characteristic fused gamma-pyrone core, and a protease homologue performs the exo-methylene formation.