Table 8.1(continued)CropPlanttissueSterilization methodemployedStrategy of planttissue inoculationIsolation mediumAntimicrobialsupplementedto growthmediumNumber ofrecoveredendophyticactinobacterialisolatesIdentification ofendophyticactinobacterial isolatesReferencesPotato plants(SoIanumtuberosumcvDesiré)Rootsand stemsSodiumhypochlorite 1%supplemented withTween-20 0.02% for1 minEthanol 70% for1 min3 times washing inthiosulfate/Ringer’ssolution for 1 minIncubation ofgrounded materialwith 120 mMsodium phosphate(pH 8) for 2 hCut into pieces ofca. 0.3 cm andmaceratedIncubated for 2 h atroom temperaturewith sodiumphosphate (pH 8)120 mMTSA (0.05x)R2A agarCycloheximide(100μg/mL)N.i.Nocardia globerulaCorynebacteriumaquaticumGarbeva et al.(^2001)Canola (Brassicanapuscv.Westar)RootsEthanol 95% for1 minAcidified mercuricchloride 0.1% (w/v)for 1 minWashed 10 timeswith sterile tapwaterRoots suspended in1/10 PBS,macerated andserially dilutedTrypticase soy broth0.3% (TSB) with 1.5%agarNone65Arthrobacterspp.Curtobacterspp.Micrococcusspp.Rathayibacterspp.Germida et al.(^1998)
(continued)170 M.F. Carvalho et al.