Abstract

Bacillus amyloliquefaciens ssp. plantarum FZB42 represents the prototype of Gram-positive plant growth promoting and biocontrol bacteria. In this study, we applied transposon mutagenesis to generate a transposon library, which was screened for genes involved in multicellular behavior and biofilm formation on roots as a prerequisite of plant growth promoting activity. Transposon insertion sites were determined by rescue-cloning followed by DNA sequencing. As in B. subtilis, the global transcriptional regulator DegU was identified as an activator of genes necessary for swarming and biofilm formation, and the DegU-mutant of FZB42 was found impaired in efficient root colonization. Direct screening of 3,000 transposon insertion mutants for plant-growth-promotion revealed the gene products of nfrA and RBAM_017140 to be essential for beneficial effects exerted by FZB42 on plants. We analyzed the performance of GFP-labeled wild-type and transposon mutants in the colonization of lettuce roots using confocal laser scanning microscopy. While the wild-type strain heavily colonized root surfaces, the nfrA mutant did not colonize lettuce roots, although it was not impaired in growth in laboratory cultures, biofilm formation and swarming motility on agar plates. The RBAM17410 gene, occurring in only a few members of the B. subtilis species complex, was directly involved in plant growth promotion. None of the mutant strains were affected in producing the plant growth hormone auxin. We hypothesize that the nfrA gene product is essential for overcoming the stress caused by plant response towards bacterial root colonization.

Highlights

  • Enhancement of plant growth by root colonizing bacteria is well-documented [1]

  • Transposon mutagenesis in B. amyloliquefaciens FZB42 To mutagenize FZB42, we used plasmids bearing a thermosensitive origin of replication and the erythromycin resistance gene, which have been developed for B. subtilis based on the mariner Himar-1 transposon variant TnYLB-1 [19]

  • By contrast to pMarA transformants, there were no antibiotic-resistant clones detectable when B. amyloliquefaciens FZB42 pMarC transformants were streaked out on either Kan or Erm containing agar at 48uC. This suggests that 98% of the Emrr clones obtained after transformation with pMarA were a consequence of true transposition events, and less likely a result of mutations through which the temperature-sensitive plasmid replication has become temperature-resistant

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Summary

Introduction

Enhancement of plant growth by root colonizing bacteria is well-documented [1]. Plant-growth-promoting (PGP) bacilli have been commercialized as biofertilizers in recent years due to their ability to form thermostable and chemically resistant endospores, allowing preparation of durable products comparable to chemicals [2]. There is a tendency in this direction, the application of microorganisms is progressing slowly. This is probably due to the variable results obtained when microbial formulations are applied [3]. Whereas a lot of progress has been made in this regard in gram-negative bacteria, e.g. Pseudomonas fluorescens, we still need to enhance our present knowledge about PGP bacilli [6]

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