TY - JOUR
T1 - Expression analysis of the spi gene in the pock-forming plasmid pSA1.1 from Streptomyces azureus and localization of its product during differentiation
AU - Doi, Katusmi
AU - Ohyama, Yukiko
AU - Yokoyama, Eiji
AU - Nishiyama, Takashi
AU - Fujino, Yasuhiro
AU - Nagayoshi, Yuko
AU - Ohshima, Toshihisa
AU - Ogata, Seiya
N1 - Funding Information:
Acknowledgments We thank J. Ishikawa for providing plasmid pRES18 and M. Kataoka for the advice about fluorescence tagging and expression analysis. This work was funded by JSPS KAKENHI no. 10660093 and Nagase & Co., Ltd.
PY - 2012/8
Y1 - 2012/8
N2 - The sporulation inhibitory gene spi in the pockforming conjugative plasmid pSA1.1 of Streptomyces azureus was introduced into cells via a high or low copy number vector to examine the effect of gene dosage on the growth of Streptomyces lividans TK24 as a host. In transformants carrying a high spi copy number, nutrient mycelial growth was inhibited, as was morphological differentiation from substrate mycelium to aerial mycelium on solid media. The degree of inhibition depended on the spi gene dosage, but the presence of pSA1.1 imp genes, which encode negative repressor proteins for spi, relieved the inhibition. Confocal images of Spi tagged with enhanced green fluorescent protein in cells on solid media revealed that spi expression was initiated at the time of elongation of substrate mycelium, that its expression increased dramatically at septation in aerial hyphae, and that the expression was maximal during prespore formation. Expression of spi covered the whole of the hyphae, and the level of expression at the tip of the hyphae during prespore formation was about sixfold greater than during substrate mycelial growth and threefold greater than during aerial mycelial growth. Thus, localized expression of spi at particular times may inhibit sporulation until triggering imp expression to repress its inhibitory effects.
AB - The sporulation inhibitory gene spi in the pockforming conjugative plasmid pSA1.1 of Streptomyces azureus was introduced into cells via a high or low copy number vector to examine the effect of gene dosage on the growth of Streptomyces lividans TK24 as a host. In transformants carrying a high spi copy number, nutrient mycelial growth was inhibited, as was morphological differentiation from substrate mycelium to aerial mycelium on solid media. The degree of inhibition depended on the spi gene dosage, but the presence of pSA1.1 imp genes, which encode negative repressor proteins for spi, relieved the inhibition. Confocal images of Spi tagged with enhanced green fluorescent protein in cells on solid media revealed that spi expression was initiated at the time of elongation of substrate mycelium, that its expression increased dramatically at septation in aerial hyphae, and that the expression was maximal during prespore formation. Expression of spi covered the whole of the hyphae, and the level of expression at the tip of the hyphae during prespore formation was about sixfold greater than during substrate mycelial growth and threefold greater than during aerial mycelial growth. Thus, localized expression of spi at particular times may inhibit sporulation until triggering imp expression to repress its inhibitory effects.
UR - http://www.scopus.com/inward/record.url?scp=84864583802&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864583802&partnerID=8YFLogxK
U2 - 10.1007/s00253-012-4000-9
DO - 10.1007/s00253-012-4000-9
M3 - Article
C2 - 22526776
AN - SCOPUS:84864583802
SN - 0175-7598
VL - 95
SP - 707
EP - 716
JO - Applied Microbiology and Biotechnology
JF - Applied Microbiology and Biotechnology
IS - 3
ER -