TNO Microbiology and Systems biology, PO Box 360, 3700 AJ Zeist, The Netherlands.
BMC Biotechnol. 2012 Aug 27;12:57. doi: 10.1186/1472-6750-12-57.
Aspergillus niger was selected as a host for producing itaconic acid due to its versatile and tolerant character in various growth environments, and its extremely high capacity of accumulating the precursor of itaconic acid: citric acid. Expressing the CAD gene from Aspergillus terreus opened the metabolic pathway towards itaconic acid in A. niger. In order to increase the production level, we continued by modifying its genome and optimizing cultivation media.
Based on the results of previous transcriptomics studies and research from other groups, two genes : gpdA encoding the glyceraldehyde -3-dehydrogenase (GPD) and hbd1 encoding a flavohemoglobin domain (HBD) were overexpressed in A. niger. Besides, new media were designed based on a reference medium for A. terreus. To analyze large numbers of cultures, we developed an approach for screening both fungal transformants and various media in 96-well micro-titer plates. The hbd1 transformants (HBD 2.2/2.5) did not improve itaconic acid titer while the gpdA transformant (GPD 4.3) decreased the itaconic acid production. Using 20 different media, copper was discovered to have a positive influence on itaconic acid production. Effects observed in the micro-titer plate screening were confirmed in controlled batch fermentation.
The performance of gpdA and hbd1 transformants was found not to be beneficial for itaconic acid production using the tested cultivation conditions. Medium optimization showed that, copper was positively correlated with improved itaconic acid production. Interestingly, the optimal conditions for itaconic acid clearly differ from conditions optimal for citric- and oxalic acid production.
黑曲霉因其在各种生长环境中具有多功能和耐受性,以及极高的积累衣康酸前体柠檬酸的能力,被选为生产衣康酸的宿主。表达土曲霉中的 CAD 基因开启了黑曲霉中衣康酸的代谢途径。为了提高生产水平,我们继续通过修饰其基因组和优化培养介质来实现。
基于先前转录组学研究和其他小组的研究结果,我们在黑曲霉中过表达了两个基因:编码甘油醛-3-脱氢酶(GPD)的 gpdA 和编码黄素血红蛋白结构域(HBD)的 hbd1。此外,根据土曲霉的参考培养基设计了新的培养基。为了分析大量的培养物,我们开发了一种在 96 孔微量滴定板中筛选真菌转化体和各种培养基的方法。hbd1 转化体(HBD 2.2/2.5)并没有提高衣康酸的产量,而 gpdA 转化体(GPD 4.3)则降低了衣康酸的产量。使用 20 种不同的培养基,发现铜对衣康酸的生产有积极的影响。在微量滴定板筛选中观察到的效果在控制批式发酵中得到了证实。
在所测试的培养条件下,发现 gpdA 和 hbd1 转化体的性能不利于衣康酸的生产。培养基优化表明,铜与衣康酸产量的提高呈正相关。有趣的是,衣康酸生产的最佳条件与柠檬酸和草酸生产的最佳条件明显不同。