戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 cluding SbnE in staphyloferrin B and AsbA in petrobactin.
2 -stage products leading to final assembly of petrobactin.
3 escued by the addition of exogenous purified petrobactin.
4 s that are linked to citrate for assembly of petrobactin.
5  measured for vibrioferrin, rhizoferrin, and petrobactin.
6 ical studies suggested that using the native petrobactin 1b for M. hydrocarbonoclasticus-specific gro
7  A modular synthesis was developed to access petrobactin, a catechol-containing siderophore isolated
8 anthracis is responsible for biosynthesis of petrobactin, a catecholate siderophore that functions in
9                                              Petrobactin, a mixed catechol-carboxylate siderophore, i
10 , targeted inhibition of the biosynthesis of petrobactin, a virulence-associated siderophore encoded
11                                              Petrobactin, a virulence-associated siderophore produced
12 this strain demonstrated increased levels of petrobactin accumulation in the culture supernatants, su
13 , including substantial up-regulation of the petrobactin and bacillibactin BGCs in B. cereus, suggest
14                             The synthesis of petrobactin and its homologues and the first biological
15 odified expression of BGCs for zwittermicin, petrobactin, and other secondary metabolites in B. cereu
16  DeltafpuBDeltafatCD, was incapable of using petrobactin as an iron source and exhibited attenuated v
17 ies to determine the biosynthetic details of petrobactin assembly based on mutational analysis of the
18 talyzes formation of amide bonds crucial for petrobactin assembly through use of biosynthetic interme
19 ed allowing for characterization of multiple petrobactin ATP-binding cassette (ABC)-import systems.
20 ere we demonstrate the roles of two putative petrobactin binding proteins FatB and FpuA (encoded by G
21                                          The petrobactin-binding receptor FpuA is required for these
22 mutations resulted in complete abrogation of petrobactin biosynthesis when strains were grown on iron
23 tudies have revealed selected early steps in petrobactin biosynthesis, the origin of 3,4-DHBA as well
24 (DHB-SP), the first isolable intermediate in petrobactin biosynthesis.
25 iron (efeUOB), ferric citrate (fecCDEF), and petrobactin (fpbNOPQ) are induced to prevent iron defici
26                              The siderophore petrobactin harbors unique 3,4-dihydroxybenzoyl iron-lig
27                                   A range of petrobactin homologues with differing dihydroxybenzamide
28 pic characteristics of a mutant deficient in petrobactin import.
29 d ATPase proteins required for the import of petrobactin in B. anthracis.
30  the recently revised structure showing that petrobactin in fact contains a 3,4-dihydroxybenzene moti
31  the penultimate step in the biosynthesis of petrobactin, involving condensation of 3,4-dihydroxybenz
32       In Bacillus anthracis, the siderophore petrobactin is required for both growth in iron-depleted
33        In Bacillus anthracis the siderophore petrobactin is vital for iron acquisition and virulence.
34 taphyloferrin B of Staphylococcus aureus and petrobactin of Bacillus anthracis hold considerable pote
35 shown to encode the complete transporter for petrobactin (PB), a photoreactive 3,4-catecholate sidero
36 ete two siderophores, bacillibactin (BB) and petrobactin (PB), for iron acquisition via membrane-asso
37 les, the siderophores bacillibactin (BB) and petrobactin (PB).
38 ihydroxybenzoate moieties of the siderophore petrobactin, produced by B. anthracis str.
39                Here additional components of petrobactin reacquisition are described.
40  contrast, the unusual 3,4-DHBA component of petrobactin renders the siderocalin system incapable of
41 iron acquisition and play redundant roles in petrobactin transport.
42 c evidence demonstrating the role of FpuA in petrobactin uptake.
43 that FatB does not play an essential role in petrobactin uptake.
44 t for conversion of endogenous precursors to petrobactin using an in vitro system.
45 ve products of AsbB are further converted to petrobactin, verifying previously proposed convergent ro
46                       Provision of exogenous petrobactin was able to rescue the growth defect in each
47               Both the (1)H and (13)C NMR of petrobactin were consistent with the recently revised st