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1 m the colony surface into the air to form an aerial mycelium.
2 ing that culminates with the formation of an aerial mycelium.
4 tants are defective in the formation of this aerial mycelium and grow as smooth, hairless colonies.
6 rable growth defect but failed to produce an aerial mycelium and showed a significant delay in the pr
7 ifferentiation involving the formation of an aerial mycelium and the production of pigmented antibiot
8 s bacterium Streptomyces coelicolor forms an aerial mycelium as a prerequisite to sporulation, which
10 ssible that these sigma factors, involved in aerial mycelium development and stress response in the a
11 ase that contributes to the proper timing of aerial mycelium formation and antibiotic production, and
12 lated, occurring specifically at the time of aerial mycelium formation and coinciding temporally with
15 morphogenetic peptide that is important for aerial mycelium formation by the filamentous bacterium S
19 xtracellular signalling in the initiation of aerial mycelium formation in two phylogenetically distan
20 results indicate that the genetic control of aerial mycelium formation is more complex than previousl
22 g did not occur on medium non-permissive for aerial mycelium formation or in one particular developme
23 factor from conditioned medium that restores aerial mycelium formation to a mutant of Streptomyces co
25 ted, commencing approximately at the time of aerial mycelium formation, and depended on bldG and bldH
26 These observations implicate the chaplins in aerial mycelium formation, and suggest that coating of t
27 tants of S. coelicolor, which are blocked in aerial mycelium formation, regain the capacity to erect
28 llular factors involved in the initiation of aerial mycelium formation, the identification of metabol
32 time points, including those taken prior to aerial mycelium formation; this suggests that whiG may b
33 verexpression and deletion of cdgB inhibited aerial-mycelium formation, and overexpression also inhib
34 whi mutants (interrupted in morphogenesis of aerial mycelium into spores), but was absent from all bl
35 partition into prespore compartments of the aerial mycelium is controlled in part by actin- and tubu
36 subset of Sg bald mutants, which produce no aerial mycelium or spores, was restored in the presence
37 pon nutrient conditions, growth, pigment and aerial mycelium production, sporulation and dimorphic tr
38 ct that transition from vegetative growth to aerial mycelium production, the first stage of morpholog
39 constructed whiK null mutant failed to form aerial mycelium, showing that different alleles of this
42 constructed whiN null mutant failed to form aerial mycelium (the "bald" phenotype) and, as a consequ
43 pmentally regulated, increasing sharply when aerial mycelium was present, and reaching a maximum appr
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