Horizontal Transfer of Promiscuous Activity from Nonphotosynthetic Bacteria Contributed to Evolution of Chlorophyll Degradation Pathway

Mol Biol Evol. 2019 Dec 1;36(12):2830-2841. doi: 10.1093/molbev/msz193.

Abstract

The relationship between enzymes and substrates does not perfectly match the "lock and key" model, because enzymes act on molecules other than their true substrate in different catalytic reactions. Such biologically nonfunctional reactions are called "promiscuous activities." Promiscuous activities are apparently useless, but they can be an important starting point for enzyme evolution. It has been hypothesized that enzymes with low promiscuous activity will show enhanced promiscuous activity under selection pressure and become new specialists through gene duplication. Although this is the prevailing scenario, there are two major problems: 1) it would not apply to prokaryotes because horizontal gene transfer is more significant than gene duplication and 2) there is no direct evidence that promiscuous activity is low without selection pressure. We propose a new scenario including various levels of promiscuous activity throughout a clade and horizontal gene transfer. STAY-GREEN (SGR), a chlorophyll a-Mg dechelating enzyme, has homologous genes in bacteria lacking chlorophyll. We found that some bacterial SGR homologs have much higher Mg-dechelating activities than those of green plant SGRs, while others have no activity, indicating that the level of promiscuous activity varies. A phylogenetic analysis suggests that a bacterial SGR homolog with high dechelating activity was horizontally transferred to a photosynthetic eukaryote. Some SGR homologs acted on various chlorophyll molecules that are not used as substrates by green plant SGRs, indicating that SGR acquired substrate specificity after transfer to eukaryotes. We propose that horizontal transfer of high promiscuous activity is one process of new enzyme acquisition.

Keywords: STAY-GREEN; chlorophyll degradation; enzyme; horizontal gene transfer; metabolic pathway; promiscuous activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Chlorophyll / metabolism*
  • Chloroplast Proteins / genetics*
  • Chloroplast Proteins / metabolism
  • Evolution, Molecular*
  • Gene Transfer, Horizontal*
  • Magnesium / metabolism
  • Phylogeny
  • Substrate Specificity

Substances

  • Arabidopsis Proteins
  • Bacterial Proteins
  • Chloroplast Proteins
  • SGR1 protein, Arabidopsis
  • Chlorophyll
  • Magnesium