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Formulation and stabilisation of the biocontrol yeast Pichia anomala
Melin, P.; Schnürer, J.; Håkansson, S. (2010). Formulation and stabilisation of the biocontrol yeast Pichia anomala. Antonie van Leeuwenhoek 99(1): 107-112. https://dx.doi.org/10.1007/s10482-010-9522-5
In: Antonie van Leeuwenhoek. Stichting Antonie van Leeuwenhoek: Amsterdam. ISSN 0003-6072; e-ISSN 1572-9699, more
Peer reviewed article  

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Keyword
    Pichia E.C. Hansen, 1904 [WoRMS]
Author keywords
    formulation; freeze-drying; fluidised bed drying; vacuum drying; biopreservation

Authors  Top 
  • Melin, P.
  • Schnürer, J.
  • Håkansson, S.

Abstract
    The yeast Pichia anomala has antifungal activities and its potential in biocontrol and biopreservation has previously been demonstrated. To practically use an organism in such applications on a larger scale the microbe has to be formulated and stabilised. In this review we give an overview of our experience of formulating and stabilising P. anomala strain J121 in a wider perspective. The stabilisation techniques we have evaluated were liquid formulations, fluidised bed drying, lyophilisation (freeze-drying) and vacuum drying. With all methods tested it was possible to obtain yeast cells with shelf lives of at least a few months and in all cases the biocontrol activity was retained. Fluidised bed drying was dependent on the addition of cottonseed flour as a carrier during the drying process. In liquid formulations a sugar, preferentially trehalose, was a required additive. These two kinds of microbial stabilisation are easily performed and relatively inexpensive but in order to keep the cells viable the biomaterial has to be stored at cool temperatures. However, there is room for optimization, such as improving the growth conditions, or include preconditioning steps to enable the cells to produce more compatible solutes necessary to survive formulation, desiccation and storage. In contrast, lyophilisation and vacuum drying require a lot of energy and are thus expensive. On the other hand, the dried cells were mostly intact after one year of storage at 30°C. Inevitably, the choice of formulation and stabilisation techniques will be dependent also on the intended use.

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