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. Author manuscript; available in PMC: 2013 Jan 5.
Published in final edited form as: Appl Microbiol Biotechnol. 2012 Jun 6;97(1):317–328. doi: 10.1007/s00253-012-4179-9

Table 4.

Enumeration of conjugative transfer frequency (T/D) of TOL-gfpmut3b plasmid from P. putida TUM-PP12 to P. putida KT2442 by CFU, FACS, and CLSM

Methods Transconjugants (cells/cm2) Transfer frequency (T/D) Transfer frequency standard deviation
CFUa (9.73×104)a 0.82×10−1 2.16×10−2
FACSb (1.26×106)b 3.30×10−1 4.23×10−2
CLSMc (4.07×106)c 1.24×10−1 3.06×10−2

Values with different letters differ significantly (P<0.05) within column

a

CFU colony forming unit. Enumeration of cells by plating assorted destructive biofilms on plates

b

FACS fluorescent activated cell sorting. Flow cytometry enumeration of cells by using the defined gates. Four populations of D, T, R, and S in biofilms can be isolated by FACS

c

CLSM confocal laser scanning microscope. Estimation of D and R directly by using CLSM microscopy combined with quantification method of image analysis