Cultivation generally showed higher proportional levels of Pseudomonas spp. than P. phosphoreum in all storage conditions with few exceptions. It has been shown with cultivation that MA packaging enabled P. phosphoreum growth in fish products [12] while other bacterial species can dominate as well during air storage [1, 16].

The present study confirms its abundance in MA conditions and its ability to dominate under aerobic environmental condition. P. phosphoreum Talazoparib has been shown to be able to reach high numbers in aerobically stored fish such as cod, squid and haddock [1, 16, 17]. In previous shelf life studies on cod and haddock from Iceland, P. phosphoreum counts have most often been higher than Pseudomonas spp. counts [1, 16] but that GSI-IX price was not the case in this study. Discrepancy between PCR strategies and cultivation is a known phenomenon where both approaches are subjective to some degree of bias [24]. Cultivation can be biased to some extent because of different optimal growth conditions and competition between bacterial species in the culture medium, and importantly due to the presence of viable but non-cultivable cells [25]. The Malthus conductance

method is based on other principles than colony counts on agar media and the harsh condition (100% CO2) of the P. phosphoreum method might underestimate their quantity in superchilled, MAP products. As shown in this study, superchilled condition delays the growth rate of P. phosphoreum and this effect is enhanced under MA (~50% CO2). It is therefore likely that some P. phosphoreum cells from these superchilled products may be partly damaged or in such a physiological state that it prolongs the lag phase and/or slows down the growth rate, hence prolonging detection time and giving lower counts during

the Malthus incubation. With the molecular approaches, the bias can be derived from the 16S rRNA copy numbers per bacterial genome. Data on 16S rRNA copy number Mannose-binding protein-associated serine protease in the P. phosphoreum genome is not available but its close relative, P. profundum contains 15 copies while Ps. fluorescens and Sh. putrefaciens contain 5 and 8 copies, respectively (insilico.ehu.es, accessed in april 2008). Other factors such as different DNA extraction efficiency on different species or incongruity in the “”universal”" priming sites can also influence the outcome [26, 27]. The microbiological activity in a fish muscle ultimately leads to its spoilage where different bacterial species contribute to the process in different ways. Pseudomonas spp. produce NH3, esters and sulphur compounds, Sh. putrefaciens produces TMA, H2S, hypoxantine and other sulphur compounds and P. phosphoreum is able to produce hypoxantine, alcohols, TMA and ketones in particular acetoin [8, 9, 28]. These organisms are often found in small quantities in newly processed fish but typically reach high numbers during storage.