Pseudomonas-specific pqqC DGGE was performed with DNA extracted from roots of wheat at the tillering stage grown in the Reckenholz field trial 2008. The four lanes derived from four replicate field plots per line/cultivar are shown. Arrows indicate the pqqC DGGE band J, which is enriched on root profiles of conventional wheat cultivars, and bands M and N which are enriched on root profiles of the Bobwhite GM and sister lines. These bands correspond to P. fluorescens subgroup 1e (band J) and P. fluorescens subgroup 1 g (band M and N), as defined by Meyer et al. . Pm3b#1 and Pm3b#2 are the GM lines with introduced pm3b transgene, Sb#1 and Sb#2 are their respective non-GM sister lines and Bobwhite is the parental line. Frisal, Toronit and Rubli are conventional wheat cultivars. Bobwhite GM and sister lines originate from T0 GM plants regenerated from tissue cultures, sister lines lost the transgene in the T1 generation due to segregation. Seeds of GM and sister lines used in the field trial were produced in the greenhouse, seeds of Bobwhite, Frisal, Toronit and Rubli were produced in the field. m, DGGE standard marker, consisting of pqqC fragments of Pseudomonas strains (from the upper to the lower band): Pseudomonas chlororaphis LMG1245, P. fluorescens Q2-87, P. fluorescens CHA0, P. fluorescens K94.37, P. corrugata LMG2172.