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Polyphasic taxonomy of Penicillium subgenus Penicillium A ... - CBS

Polyphasic taxonomy of Penicillium subgenus Penicillium A ... - CBS

Polyphasic taxonomy of Penicillium subgenus Penicillium A ... - CBS

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and more compact than those <strong>of</strong> the other sections in<strong>subgenus</strong> <strong>Penicillium</strong>: Characteristically, the number<strong>of</strong> branches per verticil is larger and the metulae andbranches are shorter and appear clavate or swollen.Phialides have a broadly cylindrical base and a short,narrow neck. Looking superficially like Aspergillusheads in the stereomicroscope, the conidia adhere indivergent to radiating tangled chains, whereas in theother sections <strong>of</strong> <strong>subgenus</strong> <strong>Penicillium</strong> they developin parallel chains, which may become somewhattangled in age. Conidia subglobose, pear-shaped tobroadly ellipsoidal, with walls finely roughened,sometimes appearing smooth. All species produceasperphenamate and the unknown metabolite O(Svendsen and Frisvad, 1994; Frisvad et al., 1990a).The species are common in all parts <strong>of</strong> the world,with P. olsonii being more common in tropical regions.Thriving in mountainous areas <strong>of</strong> the tropics,especially c<strong>of</strong>fee estates, they also thrive in greenhousesand are common on tomatoes. P. brevicompactumand P. bialowiezense are also common onmushrooms, where they can produce conspicuousgreen colonies directly on the basidiocarps. The havealso been found in yoghurts, liver patees and manyother processed foods at low water activities. See alsothe description <strong>of</strong> the section Coronata above. Thissection only contains one series: Olsonii.The series lacks known teleomorphs state, but fewtropical strains <strong>of</strong> P. olsonii can produce large whitesclerotia (see Fig. 2 F).Fig. 7. Conidiophores and conidia <strong>of</strong> (A) <strong>Penicillium</strong>olsonii and (B) P. brevicompactum.Series Olsonii contains only three closely relatedspecies: P. olsonii, P. brevicompactum and P. bialowiezense.They differ mainly in the complexity <strong>of</strong>POLYPHASIC TAXONOMY OF SUBGENUS PENICILLIUMtheir penicilli. In P. brevicompactum and P. bialowiezensebranches are <strong>of</strong>ten single, although occasionallytwo to three <strong>of</strong> them may occur per branchingpoint, whereas typical penicilli <strong>of</strong> P. olsoniiproduce a compact verticil <strong>of</strong> up to six branches,developing on the apex and sometimes also on thesubapical part <strong>of</strong> the stipe. However, deterioratedstrains <strong>of</strong> P. olsonii produce smaller verticils <strong>of</strong>branches.Penicilli <strong>of</strong> P. olsonii are sometimes suggestive <strong>of</strong>the conidial structures from the section Inordinata(which contains only P. arenicola). The shape <strong>of</strong> thephialides and the brown colour <strong>of</strong> the colonies distinguishInordinate from the section Coronata and wehave excluded the former section from <strong>subgenus</strong><strong>Penicillium</strong>.P. brevicompactum has many synonyms. Most <strong>of</strong>these were described by Zaleski and one more wellknownspecies, P. stoloniferum, was accepted byRaper and Thom (1949). We have examined ex typestrains <strong>of</strong> P. griseobrunneum (NRRL 867), P. stoloniferum(<strong>CBS</strong> 236.51), P. hagemii (<strong>CBS</strong> 316.59), P.patris-mei (<strong>CBS</strong> 210.28) and P. brunneostoloniferum(<strong>CBS</strong> 317.59). They all have the typical morphology<strong>of</strong> P. brevicompactum and furthermore all producemycophenolic acid, brevianamide A and the Raistrickphenols and are clearly synonyms <strong>of</strong> this commonspecies. Strains <strong>of</strong> P. tabescens and P. szaferi werenot available for study, so we follow Raper and Thom(1949) and Pitt (1979) in suggesting these as synonyms<strong>of</strong> P. brevicompactum.P. volgaense (<strong>CBS</strong> 626.72) and P. brevicompactumvar. magnum (IJFM 5954) were entirely typical<strong>of</strong> P. olsonii. P. monstrosum was unavailable forstudy, but Sopps protologue indicates that this was aP. olsonii rather than a P. brevicompactum as suggestedby Raper and Thom (1949) and Pitt (1979).Using multilocus DNA sequence analysis Peterson(2004) recognized P. brevicompactum, P. olsoniiand a third clade which he assigned to P. biourgeianumZaleski. Examination <strong>of</strong> the ex-type NRRL865 <strong>of</strong> P. biourgeianum showed that it is identicalwith P. bialowiezense Peterson (2004) found that theculture NRRL 863 <strong>of</strong> P. bialowiezense is identicalwith P. polonicum. However, in our study we examinedthe ex-type <strong>of</strong> P. bialowiezense <strong>CBS</strong> 227.38,which was originally deposited at <strong>CBS</strong> by K. Zaleski.Therefore NRRL 863, which was sent later to C.Thom, can be considered a contaminant. Our examination<strong>of</strong> NRRL 863 showed that it has the typicalextrolite production <strong>of</strong> P. cyclopium. It is somewhatdifferent from P. cyclopium by its good sporulationon YES and the dark reverse on CYA.Section Roqueforti Frisvad & Samson sect. nov.Sectio generis <strong>Penicillium</strong> subgeneris <strong>Penicillium</strong>,penicillis asymmetrice terverticillatis, stipitibus rugosis,15

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