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Metabolic engineering of Aspergillus oryzae NRRL 3488 for increased production of l-malic acid
Authors:Stephen H Brown  Lena Bashkirova  Randy Berka  Tyler Chandler  Tammy Doty  Keith McCall  Michael McCulloch  Sarah McFarland  Sheryl Thompson  Debbie Yaver  Alan Berry
Institution:1. Novozymes, Inc., 1445 Drew Avenue, Davis, CA, 95618, USA
2. Novozymes A/S, Krogshoejvej 36, 2880, Bagsv?rd, Denmark
Abstract:Malic acid, a petroleum-derived C4-dicarboxylic acid that is used in the food and beverage industries, is also produced by a number of microorganisms that follow a variety of metabolic routes. Several members of the genus Aspergillus utilize a two-step cytosolic pathway from pyruvate to malate known as the reductive tricarboxylic acid (rTCA) pathway. This simple and efficient pathway has a maximum theoretical yield of 2 mol malate/mol glucose when the starting pyruvate originates from glycolysis. Production of malic acid by Aspergillus oryzae NRRL 3488 was first improved by overexpression of a native C4-dicarboxylate transporter, leading to a greater than twofold increase in the rate of malate production. Overexpression of the native cytosolic alleles of pyruvate carboxylase and malate dehydrogenase, comprising the rTCA pathway, in conjunction with the transporter resulted in an additional 27 % increase in malate production rate. A strain overexpressing all three genes achieved a malate titer of 154 g/L in 164 h, corresponding to a production rate of 0.94 g/L/h, with an associated yield on glucose of 1.38 mol/mol (69 % of the theoretical maximum). This rate of malate production is the highest reported for any microbial system.
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