ライフサイエンスコーパス: merodiploid

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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 e, virB11 delta1-156, was transdominant in a merodiploid assay, indicating that the C-terminal half o

4 was transdominant over wild-type virB11 in a merodiploid assay, providing strong evidence that at lea

5 In complementation analyses, BRM18 merodiploids bearing the wild-type fauA gene in trans re

6 ables analysis of mutant RNAP derivatives in merodiploid cells (mNET-seq), we analyze transcriptional

7 plasmids, while the motile MS17 clone was a merodiploid containing single tandem chromosomal copies

8 If the merodiploid expression pattern was unchanged from that s

9 A merodiploid ferredoxin-NADP reductase mutant produced co

10 Only strains merodiploid for ccmABCDG were found after attempting to

11 Photobacterium mandapamensis was found to be merodiploid for the lux genes, and the second set of lux

12 However, alginate production by merodiploids formed in the algX::Tn501 mutant using an a

13 Merodiploid lux-rib strains of P. leiognathi were detect

14 The resulting merodiploid mutants showed constitutive partial derepres

15 Second, using 5' merodiploid native-elongating-transcript sequencing, 5'

16 N. gonorrhoeae resulted in the formation of merodiploids, showing that even with more than one chrom

17 umbers than the wild-type parent strain or a merodiploid (sodC+ sodC) strain after infection of immun

18 ophic growth resulted in the generation of a merodiploid species (but not full segregation), indicati

19 rium and the first indication that a natural merodiploid state in bacteria can correlate with geograp

20 l rates of beta-galactosidase synthesis in a merodiploid strain carrying a single-copy lambda[phi(ser

21 eri, controlled hyperexpression of CsrA in a merodiploid strain did not significantly alter the prote

22 coli cells in real time by microculture of a merodiploid strain expressing green fluorescent protein

23 ized and placed into B. subtilis to create a merodiploid strain for these genes.

24 A merodiploid strain producing elevated levels of phosphor

25 We have constructed a merodiploid strain that expresses both FtsQ and the fusi

26 When a merodiploid strain was created that carries both interru

27 We have constructed a merodiploid strain with a wild-type copy of ftsI at the

28 library of genomic DNA from a representative merodiploid strain, lnuch.13.1.

29 Using a zur merodiploid strain, we obtained two cis-acting mutations

30 types were complemented in a DeltaclpP/clpP+ merodiploid strain.

31 in conjunction with a specially constructed merodiploid strain.

32 In merodiploid strains carrying deletion or insertion mutat

33 Merodiploid strains co-expressing a constitutive VirA al

34 We also demonstrate that merodiploid strains co-expressing constitutive VirA muta

35 on or T-pilus production: (i) virB11/virB11* merodiploid strains expressing all class II and III domi

36 ays of sigmaE activity in sigE, sigE335, and merodiploid strains indicate that the residual prosequen

37 Insertion mutagenesis in parent and pcsB(+) merodiploid strains indicated that pcsB is essential in

38 We constructed merodiploid strains of P. aeruginosa containing the nati

39 a(B) activity displays this activity in rsbS merodiploid strains only when cotranscribed with rsbT an

40 e geographic sampling range, whereas lux-rib merodiploid strains were found only in coastal waters of

41 n after using the plasmid clones to generate merodiploid strains with interrupted and uninterrupted c

42 lginate production was also recovered when a merodiploid that generated a complete alginate gene clus

43 Genetic studies showed that in argP/argP(+) merodiploids, the mutated argP allele is dominant.

44 t attempted inactivation of resT resulted in merodiploid transformants, suggesting that resT is requi

45 d that a vast majority of MtrA overproducing merodiploids were associated with lysosomal associated m

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