Chatterjee Champak, Miller Leah M, Leung Yong L, Xie Lili, Yi Myongsin, Kelleher Neil L, van der Donk Wilfred A
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
J Am Chem Soc. 2005 Nov 9;127(44):15332-3. doi: 10.1021/ja0543043.
Lacticin 481 synthetase (LctM) catalyzes the ATP-dependent conversion of a ribosomally synthesized peptide to a polycyclic thioether antibiotic. It is a bifunctional enzyme that dehydrates four Ser/Thr residues to the corresponding dehydro amino acids and catalyzes the conjugate addition of Cys residues to these dehydro residues in a regio- and stereoselective process. We show here that incubation of truncated substrates with LctM results in products that are phosphorylated in the region of dehydration. Furthermore, synthetic peptides containing phosphorylated Ser and/or Thr residues are accepted by the enzyme as substrates resulting in the elimination of phosphate and dehydro amino acid production. This activity is only observed if ADP is added as cosubstrate. These results argue strongly that the enzyme utilizes ATP to phosphorylate the Ser/Thr residues that are targeted for dehydration. ATP does not appear to be required for peptide translocation or cyclization.
乳酸链球菌素481合成酶(LctM)催化核糖体合成的肽在ATP依赖下转化为多环硫醚抗生素。它是一种双功能酶,可将四个丝氨酸/苏氨酸残基脱水生成相应的脱氢氨基酸,并在区域和立体选择性过程中催化半胱氨酸残基与这些脱氢残基的共轭加成。我们在此表明,将截短的底物与LctM一起孵育会产生在脱水区域磷酸化的产物。此外,含有磷酸化丝氨酸和/或苏氨酸残基的合成肽被该酶接受为底物,导致磷酸消除和脱氢氨基酸生成。只有添加ADP作为共底物时才会观察到这种活性。这些结果有力地表明,该酶利用ATP对靶向脱水的丝氨酸/苏氨酸残基进行磷酸化。肽的转运或环化似乎不需要ATP。