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1 in (Er)-producing organism Saccharopolyspora erythraea.
2 r macrolides when compared with wild-type S. erythraea.
3 oter/activator functions appropriately in S. erythraea.
4 known antibiotic producer Saccharopolyspora erythraea.
5 1, Nocardia farcinica, and Saccharopolyspora erythraea.
8 ere cloned in pCJR24 and overexpressed in S. erythraea after integration of the vector into the chrom
9 ulator of the ery biosynthetic genes from S. erythraea and found that this protein appears to directl
13 e cassettes, in strains of Saccharopolyspora erythraea blocked in erythromycin biosynthesis, to inves
14 d roots of five centaury species (Centaurium erythraea, C. tenuiflorum, C. littorale ssp. uliginosum,
15 mplete 6-deoxyerythronolide B synthase of S. erythraea can be replaced by functionally related domain
17 this finding, when oleG2 was expressed in S. erythraea DM, 3-O-rhamnosyl-erythronolide B and 3-O-rham
19 gene responsible for THN biosynthesis in S. erythraea E_8-7 was amplified by polymerase chain reacti
20 lide B synthase (DEBS1) of Saccharopolyspora erythraea ER720 were replaced with three heterologous AT
22 omycin-producing strain of Saccharopolyspora erythraea, for detection of hybrid glycoside formation,
23 ed-brown pigment-producing (rpp) locus in S. erythraea, generating a mutant that displayed an albino
25 etic gene (ery) cluster of Saccharopolyspora erythraea has been examined by a variety of methods, inc
26 de B (6-DEB) synthase from Saccharopolyspora erythraea, in which the methylmalonate-specifying AT6 do
28 purified from recombinant Saccharopolyspora erythraea JCB101 by a new, high-yielding procedure consi
30 genes were expressed individually in the S. erythraea mutant SGT2, which is blocked both in endogeno
32 omycin-producing strain of Saccharopolyspora erythraea, O-methyltransferases from the spinosyn biosyn
33 ified this protein (M(r) = 18 kDa) as the S. erythraea ortholog of BldD, a key regulator of developme
34 the erythromycin producer Saccharopolyspora erythraea produced several novel antibiotic erythromycin
36 rown pigment produced by a Saccharopolyspora erythraea "red variant" has been shown to contain glycos
37 e pathway was expressed in Saccharopolyspora erythraea, resulting in the conversion of erythromycin t
38 acetyltransferase AcuA of Saccharopolyspora erythraea (SacAcuA, SACE_5148) as the enzyme responsible
41 olide B was, in turn, fed to a culture of S. erythraea SGT2 (spnK), 3-O-(2',3'-bis-O-methylrhamnosyl)
42 nt amino sugar, tylM2 was integrated into S. erythraea SGT2, and the resulting strain was fed with th
43 mnosyl-erythronolide precursors using the S. erythraea strain SGT2 housing EryCIII, the desosaminyltr
44 ares well with a high-producing mutant of S. erythraea that has been incrementally enhanced over deca
45 oduced by the actinomycete Saccharopolyspora erythraea that synthesizes the macrocyclic core of the a
46 genetic manipulation and fermentation of S. erythraea, the ability to produce megalomicin in this st
47 ized by the soil bacterium Saccharopolyspora erythraea through the action of a multifunctional polyke
48 onstruction of novel mutants containing a S. erythraea transcriptional terminator within the eryAI, e
51 he availability of the genome sequence of S. erythraea will improve insight into its biology and faci
53 hydroxylase P450eryF from Saccharopolyspora erythraea with androstenedione and 9-aminophenanthrene.