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1 ctivate the nfu gene only resulted in stable merodiploids.
2 leC mutants is suppressed by a pleD301/pleD+ merodiploid and results in a similar, supermotile, cold-
3 iated homologous recombination also resolves merodiploids, and hence copy number of the region is var
4 e, virB11 delta1-156, was transdominant in a merodiploid assay, indicating that the C-terminal half o
5 was transdominant over wild-type virB11 in a merodiploid assay, providing strong evidence that at lea
6           In complementation analyses, BRM18 merodiploids bearing the wild-type fauA gene in trans re
7 ables analysis of mutant RNAP derivatives in merodiploid cells (mNET-seq), we analyze transcriptional
8  plasmids, while the motile MS17 clone was a merodiploid containing single tandem chromosomal copies
9                                       If the merodiploid expression pattern was unchanged from that s
10                                            A merodiploid ferredoxin-NADP reductase mutant produced co
11                                 Only strains merodiploid for ccmABCDG were found after attempting to
12 Photobacterium mandapamensis was found to be merodiploid for the lux genes, and the second set of lux
13              However, alginate production by merodiploids formed in the algX::Tn501 mutant using an a
14                                              Merodiploid lux-rib strains of P. leiognathi were detect
15                                The resulting merodiploid mutants showed constitutive partial derepres
16                             Second, using 5' merodiploid native-elongating-transcript sequencing, 5'
17  N. gonorrhoeae resulted in the formation of merodiploids, showing that even with more than one chrom
18 umbers than the wild-type parent strain or a merodiploid (sodC+ sodC) strain after infection of immun
19 ophic growth resulted in the generation of a merodiploid species (but not full segregation), indicati
20 rium and the first indication that a natural merodiploid state in bacteria can correlate with geograp
21 del, we developed a genetic system involving merodiploid states of PfATP4 in which the endogenous gen
22 l rates of beta-galactosidase synthesis in a merodiploid strain carrying a single-copy lambda[phi(ser
23 eri, controlled hyperexpression of CsrA in a merodiploid strain did not significantly alter the prote
24 coli cells in real time by microculture of a merodiploid strain expressing green fluorescent protein
25 ized and placed into B. subtilis to create a merodiploid strain for these genes.
26 neous resistant M. tuberculosis mutants in a merodiploid strain harbouring two LpqY-SugA-SugB-SugC co
27                                            A merodiploid strain producing elevated levels of phosphor
28                        We have constructed a merodiploid strain that expresses both FtsQ and the fusi
29                                       When a merodiploid strain was created that carries both interru
30                        We have constructed a merodiploid strain with a wild-type copy of ftsI at the
31 library of genomic DNA from a representative merodiploid strain, lnuch.13.1.
32                                  Using a zur merodiploid strain, we obtained two cis-acting mutations
33                                 Using a sigM merodiploid strain, we selected for suppressor mutations
34 types were complemented in a DeltaclpP/clpP+ merodiploid strain.
35  in conjunction with a specially constructed merodiploid strain.
36                                           In merodiploid strains carrying deletion or insertion mutat
37                                              Merodiploid strains co-expressing a constitutive VirA al
38                     We also demonstrate that merodiploid strains co-expressing constitutive VirA muta
39 on or T-pilus production: (i) virB11/virB11* merodiploid strains expressing all class II and III domi
40 ays of sigmaE activity in sigE, sigE335, and merodiploid strains indicate that the residual prosequen
41  Insertion mutagenesis in parent and pcsB(+) merodiploid strains indicated that pcsB is essential in
42                               We constructed merodiploid strains of P. aeruginosa containing the nati
43 a(B) activity displays this activity in rsbS merodiploid strains only when cotranscribed with rsbT an
44 e geographic sampling range, whereas lux-rib merodiploid strains were found only in coastal waters of
45 n after using the plasmid clones to generate merodiploid strains with interrupted and uninterrupted c
46 lginate production was also recovered when a merodiploid that generated a complete alginate gene clus
47  Genetic studies showed that in argP/argP(+) merodiploids, the mutated argP allele is dominant.
48 t attempted inactivation of resT resulted in merodiploid transformants, suggesting that resT is requi
49 d that a vast majority of MtrA overproducing merodiploids were associated with lysosomal associated m