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Background: GlgE is a maltosyltransferase involved in bacterial ␣-glucan biosynthesis and is a genetically validated antituberculosis target. Results: We have determined the catalytic properties of Streptomyces coelicolor GlgE and solved its structure. Conclusion:The enzyme has the same catalytic properties as Mycobacterium tuberculosis GlgE and the structure reveals how GlgE functions. Significance: The structure will help guide the development of inhibitors with therapeutic potential.

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At least 17 kb of DNA from the large unisolatable Streptomyces coelicolor A3(2) plasmid SCP1 are concerned with methylenomycin biosynthesis. Mutational cloning analysis, using insert‐directed integration of att site deleted phage vectors into an SCP1‐containing host, provided evidence of two large transcription units, of at least 6.6 kb and 9.5 kb. At the leftmost apparent end of the larger (left‐hand) transcription unit is a region apparently involved in negative regulation of methylenomycin biosynthesis: when fragments from this region were used to direct phage integration, marked overproduction of methylenomycin resulted. The methylenomycin resistance determinant is located at the rightmost end of this same transcription unit. Hybridisation analysis with 13 kb of the cloned mmy region showed that it was closely similar to a segment of pSV1, a plasmid that specifies methylenomycin biosynthesis in S. violaceus‐ruber SANK 95570.

The whiA sporulation gene of Streptomyces coelicolor A3(2), which plays a key role in switching aerial hyphae away from continued extension growth and toward sporulation septation, was cloned by complementation of whiA mutants. DNA sequencing of the wild-type allele and five whiA mutations verified that whiA is a gene encoding a protein with homologues in all gram-positive bacteria whose genome sequence is known, whether of high or low G؉C content. No function has been attributed to any of these WhiA-like proteins. In most cases, as in S. coelicolor, the whiA-like gene is downstream of other conserved genes in an operon-like cluster. Phenotypic analysis of a constructed disruption mutant confirmed that whiA is essential for sporulation. whiA is transcribed from at least two promoters, the most downstream of which is located within the preceding gene and is strongly up-regulated when colonies are undergoing sporulation. The up-regulation depends on a functional whiA gene, suggesting positive autoregulation, although it is not known whether this is direct or indirect. Unlike the promoters of some other sporulation-regulatory genes, the whiA promoter does not depend on the sporulation-specific factor encoded by whiG.Dispersal of the mycelial organism Streptomyces coelicolor A3(2) occurs by the formation of long chains of spores from aerial hyphae. A critical stage in this process is the subdivision of a multigenomic apical aerial hyphal compartment into many unigenomic prespore compartments by the synchronous formation of regularly spaced sporulation septa (26,38). At least six genetic loci (whiA, whiB, whiG, whiH, whiI, and whiJ) are needed for sporulation septation (8, 10), in addition to cell division genes that are also involved in vegetative growth (24,25). These six early whi loci appear to play no role in vegetative growth. Mutations in them have pleiotropic effects on the later stages of sporulation, including weak or undetectable transcription of the genes responsible for the production of grey spore pigment (20), hence the white colony phenotype after which they were named (18). Transcription of sigF, which encodes a late sporulation sigma factor, is also dependent on these early whi genes (21, 28). The complex early whi mutant phenotypes suggest that some or all of the six "early" whi genes encode regulatory elements. Indeed, whiG encodes a sigma factor ( WhiG [11,37]), whiH encodes a repressor-like protein (31), and whiI encodes a response regulator-like protein (1); the product of whiB has features that resemble those of some transcription factors (13,34). Mutations in some other more recently discovered genes also affect sporulation septation but in a more allele-specific manner (30).This paper is concerned with whiA. Like whiB mutants, whiA and whiA whiB double mutants have tightly coiled aerial hyphae that are markedly longer than normal spore chains, contain uncondensed DNA, and lack sporulation septa and readily detectable FtsZ (9, 15, 33). whiA and whiB are therefore believed to play a role in th...

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Glucose kinase in Streptomyces coelicolor has a molecular weight of about 110,000. In crude extracts, the enzyme exhibited apparent Km values of 0.20 mM for ATP, 0.27 mM for glucose, and 2.2 mM for the glucose analogue 2-deoxyglucose. Mutations (glk) to 2-deoxyglucose-resistance, which greatly reduce glucose kinase activity and result in relief of glucose repression of utilisation of various carbon sources, were mapped between proA and hisA in the S. coelicolor linkage map. Glucose kinase activity, 2-deoxyglucose-sensitivity, glucose utilisation and glucose repression, were all restored to glk mutants by a 3.5 kb DNA fragment cloned from S. coelicolor into a phage vector (phi C31 KC515), and by larger (10-30 kb) fragments cloned into a low copy number plasmid vector (pIJ916). The glk gene was further localised to a 2.9 kb BclI fragment of the cloned DNA by sub-cloning. Part or all of this fragment was present in each of five primary plasmid clones tested.

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