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Coa3-null mutant was constructed as described in Mick et al.33.33
S. coelicolor ΔnucS (gene SCO5388, nucSSco) in-frame deletion mutant was constructed by double crossover recombination using the plasmid pIJ6650 (ref. 40).
Finally, a D52N mutant was constructed introducing an N-glycosylation sequence at an area central to the CR2 dimer interface.
A pyruvate decarboxylase (Pdc -deficient mutant was constructed and evolved for raPdc -deficientnsumutant washout ethanol produ
A D95A mutant was constructed as a negative control to substitute for W93A.
The RR02 mutant was constructed by Hancock and Perego [27].
The mprF insertionnal mutant was constructed following another procedure.
For lmo2123 also a deletion mutant was constructed.
A bipD mutant was constructed by single crossover insertional mutagenesis.
The bacterial mutant was constructed by double crossover method using the construct as mentioned previously [17].
The C129S mutant was constructed by site directed mutagenesis and confirmed with direct sequencing (LGTC).
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