Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Sapporo, Hokkaido, Japan.
AIST-Waseda University Computational Bio Big-Data Open Innovation Laboratory (CBBD-OIL), AIST, Waseda University, Tokyo, Japan.
Microbiologyopen. 2022 Apr;11(2):e1280. doi: 10.1002/mbo3.1280.
In most countries, genetically modified microorganisms are not approved for use for fermentation in the food industry. Therefore, random mutagenesis and subsequent screening are performed to improve the productivities of valuable metabolites and enzymes as well as other specific functions in an industrial microbial strain. In addition, targeted gene knockout is performed by genetic recombination using its enzyme genes as selectable markers to maintain self-cloning status. However, random mutagenesis has a drawback as it does not guarantee improvement of the targeted function. Conversely, self-cloning is rarely used to breed an industrial microbial strain. This is probably because a self-cloning strain is similar to a genetically modified strain, as both undergo homologous recombination, although exogenous genes are not introduced. In this article, I discuss the usefulness of genome editing technology as a substitute for conventional techniques to breed filamentous fungal strains. This article particularly focusses on "genome co-editing," a genome editing technology used for knocking out two genes concomitantly, as reported in Magnaporthe grisea and Aspergillus oryzae. Especially, when genome co-editing is applied to a target gene and a membrane transporter gene that aid the entry of toxic compounds into cells, the resulting clone can be categorized as an autotrophic and non-genetically modified clone. Such a clone should easily apply to industrial fermentation without being restricted by a genetically modified status. Genome co-editing will also be used to construct mutant strains with multiple target gene knockouts by eliminating multiple membrane transporter genes. This could substantially improve the productivities of valuable metabolites and enzymes in a stepwise manner. Thus, genome co-editing is considered a potentially powerful method to knock out single or multiple target genes that can contribute to the breeding of filamentous fungal strains in the food industry.
在大多数国家,转基因微生物未经批准不得用于食品工业发酵。因此,通常采用随机诱变和后续筛选来提高工业微生物菌株中目标代谢物和酶以及其他特定功能的生产力。此外,通过使用其酶基因作为选择性标记的遗传重组进行靶向基因敲除,以维持自我克隆状态。然而,随机诱变存在一个缺点,因为它不能保证目标功能的改进。相反,自我克隆很少用于培育工业微生物菌株。这可能是因为自我克隆菌株与基因修饰菌株相似,因为两者都经历同源重组,尽管没有引入外源基因。在本文中,我讨论了基因组编辑技术作为传统技术的替代品在培育丝状真菌菌株中的有用性。本文特别关注“基因组共编辑”,这是一种用于同时敲除两个基因的基因组编辑技术,如在稻瘟病菌和米曲霉中报道的那样。特别是,当将基因组共编辑应用于有助于有毒化合物进入细胞的靶基因和膜转运蛋白基因时,产生的克隆可以归类为自养和非基因修饰的克隆。这样的克隆应该很容易适用于工业发酵,而不受基因修饰状态的限制。基因组共编辑还将用于通过消除多个膜转运蛋白基因来构建具有多个靶基因敲除的突变株。这可以逐步显著提高有价值代谢物和酶的生产力。因此,基因组共编辑被认为是一种潜在的强大方法,可以敲除单个或多个目标基因,有助于在食品工业中培育丝状真菌菌株。