Activity-Based Protein Profiling of Ammonia Monooxygenase in Nitrosomonas europaea

Abstract

Nitrosomonas europaea is an aerobic nitrifying bacterium that oxidizes ammonia (NH 3 ) to nitrite (NO 2 − ) through the sequential activities of ammonia monooxygenase (AMO) and hydroxylamine dehydrogenase (HAO). Many alkynes are mechanism-based inactivators of AMO, and here we describe an activity-based protein profiling method for this enzyme using 1,7-octadiyne (17OD) as a probe. Inactivation of NH 4 + -dependent O 2 uptake by N. europaea by 17OD was time- and concentration-dependent. The effects of 17OD were specific for ammonia-oxidizing activity, and de novo protein synthesis was required to reestablish this activity after cells were exposed to 17OD. Cells were reacted with Alexa Fluor 647 azide using a copper-catalyzed azide-alkyne cycloaddition (CuAAC) (click) reaction, solubilized, and analyzed by SDS-PAGE and infrared (IR) scanning. A fluorescent 28-kDa polypeptide was observed for cells previously exposed to 17OD but not for cells treated with either allylthiourea or acetylene prior to exposure to 17OD or for cells not previously exposed to 17OD. The fluorescent polypeptide was membrane associated and aggregated when heated with β-mercaptoethanol and SDS. The fluorescent polypeptide was also detected in cells pretreated with other diynes, but not in cells pretreated with structural homologs containing a single ethynyl functional group. The membrane fraction from 17OD-treated cells was conjugated with biotin-azide and solubilized in SDS. Streptavidin affinity-purified polypeptides were on-bead trypsin-digested, and amino acid sequences of the peptide fragments were determined by liquid chromatography-mass spectrometry (LC-MS) analysis. Peptide fragments from AmoA were the predominant peptides detected in 17OD-treated samples. In-gel digestion and matrix-assisted laser desorption ionization–tandem time of flight (MALDI-TOF/TOF) analyses also confirmed that the fluorescent 28-kDa polypeptide was AmoA.

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 15, 2016
Source ID
10.1128/aem.03556-15

Entities

People

  • Aaron T. Wright
  • Chris Yeager
  • Kristen Bennett
  • Michael R Hyman
  • Natalie C. Sadler

Organizations

  • Los Alamos National Laboratory
  • North Carolina State University
  • Pacific Northwest National Laboratory
  • Strategic Environmental Research and Development Program

Tags

Fields of Study

  • Biology
  • Chemistry

Readers

  • Analytical Chemistry
  • Molecular and Cellular Biochemistry
  • Organic Chemistry

Technology Areas

  • Directed Energy