Transformation of pichia methanolica
AssigneeZymoGenetics, Inc.
InventorsChristopher K. Raymond, Susan D. Holderman, Erica Vanaja
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AssigneeZymoGenetics, Inc.
InventorsChristopher K. Raymond, Susan D. Holderman, Erica Vanaja
Estimating the term…
Methods for transforming Pichia methanolica, and DNA molecules useful in transformation of P. methanolica, are disclosed. P. methanolica cells are exposed, in the presence of DNA molecules, to a pulsed electric field having a field strength of from 2.5 to 4.5 kV/cm and a pulse duration of from 1 to 40 milliseconds, whereby the DNA molecules are introduced into the cells. The DNA molecules may comprise an expression unit that includes a transcription promoter of a P. methanolica gene operably linked to a segment encoding a polypeptide or protein of interest. The DNA molecules may also encode a selectable marker, such as a P. methanolica ADE2 gene. Cells transformed according to the invention may be used in production systems for the preparation of proteins of commercial importance.
A method for introducing DNA into a Pichia methanolica (P. methanolica) cell, comprising exposing said Pichia methanolica cell, in the presence of a linear DNA molecule, to an exponentially decaying, pulsed electric field having a field strength of from 2.5 to 4.5 kV/cm and a time constant of from 15 to 40 milliseconds, whereby said linear DNA molecule is introduced into said cell.
A method for transforming P. methanolica cells with heterologous DNA, comprising exposing a population of said P. methanolica cells, in the presence of heterologous linear DNA molecules, to an exponentially decaying, pulsed electric field having a field strength of from 2.5 to 4.5 kV/cm and a time constant of from 15 to 40 milliseconds, whereby said heterologous DNA is introduced into at least a portion of said population, and recovering cells into which said DNA has been introduced.
Dependencies are inferred from the claim text.