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1 as been cloned, expressed, and purified in a heterologous host.
2 lly activate silent gene clusters in a model heterologous host.
3 modular carbon-fixing microcompartments in a heterologous host.
4 to induce sac-like outgrowths on petals in a heterologous host.
5 e components of these defense compounds in a heterologous host.
6 ylneuraminic acid levels when expressed in a heterologous host.
7 e under physiological conditions albeit in a heterologous host.
8 rotein expression of the target protein in a heterologous host.
9 ey allowed production of the antibiotic in a heterologous host.
10 myces lividans, a genetically well developed heterologous host.
11 ical testing and by expressing the gene in a heterologous host.
12 unctional expression of the beta-lactam in a heterologous host.
13 assembling complex biosynthetic pathways in heterologous hosts.
14 resistance to capuramycins when expressed in heterologous hosts.
15 wards re-construction of natural pathways in heterologous hosts.
16 enhancing NP production in these engineered heterologous hosts.
17 anisms or difficult-to-manipulate strains in heterologous hosts.
18 r the unique behavior of Mu transposition to heterologous hosts.
19 ing sustainable production of salidroside in heterologous hosts.
20 etic or chimeric constructs, often tested in heterologous hosts.
21 mes as they enable precise genome editing in heterologous hosts.
22 ficient production of high-value products in heterologous hosts.
23 ogy approach to reconstitute, in a nonnative heterologous host, a minimal machinery capable of buildi
24 tracellular proteins of M. tuberculosis in a heterologous host and allows ready evaluation of their b
25 rase domain; (ii) the PKSs are functional in heterologous hosts, and coexpression with an enediyne th
26 sion of high reduction potential laccases in heterologous hosts, and issues regarding enzyme glycosyl
27 basidiomycete natural products in ascomycete heterologous hosts, and open up new possibilities of fur
28 ssion of engineered proteins in a variety of heterologous hosts; and mass spectrometry-based high-thr
29 genes required to produce aklanonic acid in heterologous hosts are dpsG (ACP), dauI (regulatory acti
32 ed for transcriptional regulation in various heterologous host cells, offers unprecedented ease in de
33 oimmunoprecipitate from Drosophila heads and heterologous host cells, suggesting that they interact i
36 were carried out with C6 rat glioma cells, a heterologous host chosen for its known deficiency in gan
37 S. meliloti alpha functions are conserved in heterologous host E. coli even though the two alpha subu
39 to erythromycin) production in three common heterologous hosts (E. coli, Bacillus subtilis, and S. c
40 some encodes synthesis of the pigment in the heterologous host, Erwinia carotovora, demonstrating, fo
41 In addition to expressing the cluster in the heterologous host Escherichia coli, which confers the ab
42 ype KatG and KatG(S315T) were expressed in a heterologous host (Escherichia coli) and purified to hom
43 NAP by co-overexpression and assembly in the heterologous host, Escherichia coli, have been described
46 ining, to clone them, and to express them in heterologous hosts in much higher throughput than before
47 Reconstitution of biosynthetic pathways in a heterologous host is a promising strategy for rapid and
48 y for conferring replication competence in a heterologous host is important to an understanding of th
49 The expression of functional proteins in heterologous hosts is a cornerstone of modern biotechnol
50 s CHCC1524 was functionally expressed in the heterologous host Lactococcus lactis NZ9000, and the ben
51 lled expression of AS in E. faecalis and the heterologous host Lactococcus lactis, experiments were d
52 ntire mycaminose biosynthetic machinery in a heterologous host led to the discovery of a previously o
53 mediate transcriptional derepression in the heterologous host Mycobacterium smegmatis in a way that
55 ute plant terpenoid biosynthetic pathways in heterologous host organisms as a functional discovery to
56 a protocol for isolating GVs from native and heterologous host organisms, functionalizing these nanos
57 was expressed in good yields cultivating the heterologous host Pichia pastoris on the 5L bioreactor s
58 of these lineages appear to be shared among heterologous hosts providing evidence of interspecies tr
59 grative plasmid and subsequent expression in heterologous hosts revealed that considerable amounts of
60 e C-methylation, we employed the rarely used heterologous host Rhizobium leguminosarum to invoke the
61 ty of intramuscular (i.m.) immunization with heterologous-host rotavirus (simian strain RRV) to induc
62 i.m.) inoculation of mice with homologous or heterologous host rotaviruses to induce protection from
63 nteraction because expression of Hwp1 in the heterologous host S. cerevisiae permits adherence to wil
64 lized properly at the plasma membrane in the heterologous host Saccharomyces cerevisiae, but some var
65 We demonstrate that cleavage occurs in a heterologous host, Saccharomyces cerevisiae, deficient i
66 Reconstitution of 6-methylpretetramid in a heterologous host sets the stage for a more systematic i
70 rred pathway was genetically refactored in a heterologous host, Streptomyces coelicolor CH999, to pro
71 s native hosts to more industrially-amenable heterologous hosts such as Escherichia coli, Saccharomyc
72 s in both the native producer S. griseus and heterologous hosts, such as S. albus and S. lividans.
75 Expression of full-length E. faecalis Esp in heterologous host systems of esp-deficient Lactococcus l
77 nsposable element Ac is highly active in the heterologous hosts tobacco and tomato, but shows very mu
78 vative was generated, demonstrating that our heterologous host/vector pair can be a useful platform t
79 nature of the inoculum (e.g., homologous or heterologous host virus and live or inactivated virus),
81 s suggest B. subtilis and E. coli are better heterologous hosts when compared to S. cerevisiae and th
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