Two novel homologous proteins of Streptomyces coelicolor and Streptomyces lividans are involved in the formation of the rodlet layer and mediate attachment to a …

D Claessen, HAB Wösten, G Keulen… - Molecular …, 2002 - Wiley Online Library
Molecular microbiology, 2002Wiley Online Library
The filamentous bacteria Streptomyces coelicolor and Streptomyces lividans exhibit a
complex life cycle. After a branched submerged mycelium has been established, aerial
hyphae are formed that may septate to form chains of spores. The aerial structures possess
several surface layers of unknown nature that make them hydrophobic, one of which is the
rodlet layer. We have identified two homologous proteins, RdlA and RdlB, that are involved
in the formation of the rodlet layer in both streptomycetes. The rdl genes are expressed in …
Summary
The filamentous bacteria Streptomyces coelicolor and Streptomyces lividans exhibit a complex life cycle. After a branched submerged mycelium has been established, aerial hyphae are formed that may septate to form chains of spores. The aerial structures possess several surface layers of unknown nature that make them hydrophobic, one of which is the rodlet layer. We have identified two homologous proteins, RdlA and RdlB, that are involved in the formation of the rodlet layer in both streptomycetes. The rdl genes are expressed in growing aerial hyphae but not in spores. Immunolocalization showed that RdlA and RdlB are present at surfaces of aerial structures, where they form a highly insoluble layer. Disruption of both rdlA and rdlB in S. coelicolor and S. lividans (ΔrdlAB strains) did not affect the formation and differentiation of aerial hyphae. However, the characteristic rodlet layer was absent. Genes rdlA and rdlB were also expressed in submerged hyphae that were in contact with a hydrophobic solid. Attachment to this substratum was greatly reduced in the ΔrdlAB strains. Sequences homologous to rdlA and rdlB occur in a number of streptomycetes representing the phylogenetic diversity of this group of bacteria, indicating a general role for these proteins in rodlet formation and attachment.
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