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1 e, in heat resistance and in the presence of dipicolinic acid.
2 ine but not with a 1:1 chelate of Ca(2+) and dipicolinic acid.
3 s dodecylamine and a 1:1 chelate of Ca2+ and dipicolinic acid.
4 ns but were much lower in spores that lacked dipicolinic acid.
5 at 1010 cm(-)(1), which is characteristic of dipicolinic acid.
6 he initiation of accumulation of the spore's dipicolinic acid.
7 z = +74 peak when ionized in the presence of dipicolinic acid.
8 what different from those of proteins and Ca-dipicolinic acid.
9     Our results confirm prior assignments of dipicolinic acid, amino acids, and calcium complex ions
10 actility and the level of the 1:1 chelate of dipicolinic acid and Ca(2+) (CaDPA) were monitored by ph
11 s, with variable time delays, the release of dipicolinic acid and cations from the spore core--a key
12 he release of the spore core's huge depot of dipicolinic acid and cations, and replacement of these c
13 ot due to the dormant spore's high levels of dipicolinic acid and divalent cations.
14 f the tightly bound Zn(2+) by treatment with dipicolinic acid and EDTA at pH 6.0 resulted in almost c
15 of taxonomically important compounds such as dipicolinic acid and fatty acids.
16 d a protein channel governing the release of dipicolinic acid and hydration of the spore core during
17  their cortex is accompanied by excretion of dipicolinic acid and uptake of some core water.
18  in spore-specific molecules (in particular, dipicolinic acid) and uptake of the nucleic acid stain.
19 tain prominent peaks attributed to arginine, dipicolinic acid, and glutamic acid, but the shot-to-sho
20                            Free amino acids, dipicolinic acid, and unidentified small molecules were
21  the complete release of the spore component dipicolinic acid, are achieved without the restoration o
22 oss of spore refractility and the release of dipicolinic acid but no degradation of cortex peptidogly
23 rminated cwlD spores that had excreted their dipicolinic acid but where cytoplasmic water content had
24 trients, KCl, or a 1:1 chelate of Ca(2+) and dipicolinic acid (Ca-DPA), and the colony-forming effici
25  used to simultaneously measure levels of Ca-dipicolinic acid (CaDPA) and changes in spore morphology
26  kinetic parameters of the release of Ca(2+)-dipicolinic acid (CaDPA) during germination of spore pop
27                       Release of Ca(2+) with dipicolinic acid (CaDPA) was monitored by Raman spectros
28 ed by the electric field and release calcium dipicolinic acid (CaDPA), a biomarker molecule present a
29 reover, TprC(Fl) increased efflux of terbium-dipicolinic acid complex from large unilamellar vesicles
30                                Using terbium-dipicolinic acid complex-loaded large unilamellar vesicl
31      Structural evidence and the presence of dipicolinic acid demonstrate that phase-bright offspring
32   The biosynthetic precursor to DPA, dihydro-dipicolinic acid (DHDPA), is produced by DHDPA synthase
33    A neutral anion binding receptor based on dipicolinic acid diamide was equipped with thiol groups
34 -alanine and the 1:1 chelate of Ca(2)(+) and dipicolinic acid, did not mediate spore-to-spore communi
35           On the basis of SERS measurements, dipicolinic acid displays the strongest binding to the A
36 gh salt concentrations, Triton X-100, Ca(2+)-dipicolinic acid, dithiothreitol, or peptidoglycan diges
37 ceptors, including a 1:1 chelate of Ca2+ and dipicolinic acid, dodecylamine, lysozyme in hypertonic m
38 s with a mutation in spoVF cannot synthesize dipicolinic acid (DPA) and are too unstable to be purifi
39            Metal-chelating reagents, such as dipicolinic acid (DPA) and ethylenediaminetetraacetic ac
40        ger3 spoVA and sleB spoVA spores lack dipicolinic acid (DPA) and have lower core wet densities
41            Rapid and accurate testing of 2,6-dipicolinic acid (DPA) and levofloxacin (LFX) has been a
42  for spore integrity and resistance, such as dipicolinic acid (DPA) and the spore's inner membrane.
43 is reported for the ratiometric detection of dipicolinic acid (DPA) and uric acid (UA).
44 ve irradiated spores, showed the presence of dipicolinic acid (DPA) as well as various lipids.
45 triple mutant exhibited a pronounced loss of dipicolinic acid (DPA) between hours 8 and 24 of sporula
46 ubtilis spoVF strains that cannot synthesize dipicolinic acid (DPA) but take it up during sporulation
47                                              Dipicolinic acid (DPA) comprises approximately 10% of th
48 tors the fluorescence of Tb3+ complexed with dipicolinic acid (DPA) directly in concentrated PEG solu
49  of commitment and the subsequent release of dipicolinic acid (DPA) during nutrient germination of sp
50 eins essential for the uptake and release of dipicolinic acid (DPA) during spore formation and germin
51 r the release of the spore-specific molecule dipicolinic acid (DPA) during spore germination.
52                               The release of dipicolinic acid (DPA) during the germination of Bacillu
53 e of the great majority of the large pool of dipicolinic acid (DPA) from individual spores of B. subt
54                                              Dipicolinic acid (DPA) is a major component of bacterial
55 Bacillus subtilis has shown that the spore's dipicolinic acid (DPA) level can markedly influence both
56  fluorescence of trapped Tb3+ complexed with dipicolinic acid (DPA) or by the increase of fluorescenc
57                           The small molecule dipicolinic acid (DPA) plays a central role in both the
58  forespores, gave spores that released their dipicolinic acid (DPA) via germinant receptor (GR)-depen
59                             Release of spore dipicolinic acid (DPA) was then measured by differential
60 th nutrient (l-alanine) and non-nutrient (Ca-dipicolinic acid (DPA)) germinants with a temporal resol
61                   Starting from hit fragment dipicolinic acid (DPA), 8-hydroxy- and 8-sulfonamido-qui
62 n germinate with a 1:1 chelate of Ca(2+) and dipicolinic acid (DPA), a compound present at high level
63  with the goal of improving the detection of dipicolinic acid (DPA), a major component of bacterial s
64        The Ln(DO2A)(+) binary complexes bind dipicolinic acid (DPA), a major constituent of bacterial
65 -asparagine, and a 1:1 chelate of Ca(2+) and dipicolinic acid (DPA), but not with dodecylamine, and t
66 s and initiation of rapid release of spores' dipicolinic acid (DPA), but times for release of >90% of
67                          On the basis of 2,6-dipicolinic acid (DPA), several libraries were synthesiz
68 sed of less dense spores that had lost their dipicolinic acid (DPA), undergone significant protein de
69 opy to obtain molecule-specific signals from dipicolinic acid (DPA), which is a marker molecule for b
70 ndependently and is a major factor in Ca(2+)-dipicolinic acid (DPA)-triggered germination, but its en
71 ies is release of the spores' large depot of dipicolinic acid (DPA).
72 emicals, such as a 1:1 chelate of Ca(2+) and dipicolinic acid (DPA).
73 when it interacts with the aromatic chelator dipicolinic acid (DPA).
74 mical germinant, a 1-1 chelate of Ca(2+) and dipicolinic acid (DPA).
75              Pyridine-2,6-dicarboxylic acid (dipicolinic acid [DPA]) in a 1:1 chelate with calcium io
76      Liposome fusion was monitored by the Tb/dipicolinic acid fluorescence assay for the intermixing
77 ity of vanadium complexes bearing the ligand dipicolinic acid (H(2)dipic) with alcohols has been expl
78 enes based on either isophthalic acid or 2,6-dipicolinic acid have been known for more than a decade
79 so did not produce the insecticidal compound dipicolinic acid, however, production of a yellow-colore
80  partly a result of the high level of Ca(2+)-dipicolinic acid in spores and DNA repair during spore o
81 nt spore populations, and the environment of dipicolinic acid in the core of superdormant spores as d
82 mant spores is not due to the high levels of dipicolinic acid in the spore cytoplasm, because GFP was
83 subtilis may be involved in the transport of dipicolinic acid into the forespore during sporulation a
84 through which the spore core's huge depot of dipicolinic acid is released during germination, and (iv
85 coated and cotE spores germinate poorly with dipicolinic acid is the absence of CwlJ from these spore
86 rmination, the SpoVAD protein, essential for dipicolinic acid movement across the IM, the SleB cortex
87 t spores did, however, germinate with Ca(2+)-dipicolinic acid or dodecylamine.
88 on of gerF spores with a mixture of Ca2+ and dipicolinic acid or with dodecylamine was normal, as was
89  including delayed forespore accumulation of dipicolinic acid, overexpression of forespore-specific g
90 ion (C6H3ON+) obtained from the pyrolysis of dipicolinic acid (pyridine-2,6-dicarboxylic acid; DPA),
91 roteins and the SpoVA proteins essential for dipicolinic acid release changed minimally during this p
92  or of the SpoVAD protein likely involved in dipicolinic acid release early in germination.
93 the initial stages of germination, including dipicolinic acid release.
94 eter was operated in single-ion mode enabled dipicolinic acid to be detected in 10(5) spores.
95 , sugars), and the spore-specific biomarker, dipicolinic acid, were generated by one-step thermochemo