Assessing the potential of mutational strategies to elicit new phenotypes in industrial strains

  1. Daniel Klein-Marcuschamer and
  2. Gregory Stephanopoulos*
  1. Department of Chemical Engineering, Massachusetts Institute of Technology, Room 56-469, Cambridge, MA 02139
  1. Communicated by Arnold L. Demain, Drew University, Madison, NJ, December 23, 2007 (received for review December 14, 2007)

Abstract

Industrial strains have been traditionally improved by rational approaches and combinatorial methods involving mutagenesis and selection. Recently, other methods have emerged, such as the use of artificial transcription factors and engineering of the native ones. As methods for generating genetic diversity continue to proliferate, the need for quantifying phenotypic diversity and, hence, assessing the potential of various genetic libraries for strain improvement becomes more pronounced. Here, we present a metric based on the quantification of phenotypic diversity, using Lactobacillus plantarum as a model organism. We found that phenotypic diversity can be introduced by mutagenesis of the principal σ factor, that this diversity can be modulated by tuning the sequence diversity, and that this method compares favorably with commonly used protocols for chemical mutagenesis. The results of the diversity metric here developed also correlated well with the probability of finding improved mutants in the different libraries, as determined by recursive screening under stress. In addition, we subjected our libraries to lactic and inorganic acids and found strains with improved growth in both conditions, with a concomitant increase in lactate productivity.

Footnotes

  • *To whom correspondence should be addressed. E-mail: gregstep{at}mit.edu
  • Author contributions: D.K.-M. and G.S. designed research; D.K.-M. performed research; D.K.-M. analyzed data; and D.K.-M. and G.S. wrote the paper.

  • The authors declare no conflict of interest.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0712177105/DC1.

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