Mitsuhashi S, Ohnishi J, Hayashi M, Ikeda M
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co. Ltd., Asahi-machi, Machida, 194-8533 Tokyo, Japan.
Appl Microbiol Biotechnol. 2004 Feb;63(5):592-601. doi: 10.1007/s00253-003-1402-8. Epub 2003 Aug 21.
Carbonic anhydrase catalyzes the interconversion of CO(2) and bicarbonate. We focused on this enzyme in the amino acid-producing organism Corynebacterium glutamicum in order to assess the availability of bicarbonate for carboxylation reactions essential to growth and for those required for L-lysine overproduction. A whole-genome sequence revealed two genes encoding putative beta-type and gamma-type carbonic anhydrases in C. glutamicum. These genes encode polypeptides containing zinc ligands strictly conserved in each type of carbonic anhydrase and were designated bca and gca, respectively. Internal deletion of the chromosomal bca gene resulted in a phenotype showing severely reduced growth under atmospheric conditions (0.04% CO(2)) on both complete and minimal media. The growth defect of the Delta bca strain was restored under elevated CO(2) conditions (5% CO(2)). Introduction of the red alga Porphyridium purpureum carbonic anhydrase gene ( pca) could compensate for the bca deletion, allowing normal growth under an atmospheric level of CO(2). In contrast, the Delta gca strain behaved identically to the wild-type strain with respect to growth, irrespective of the CO(2) conditions. Attempts to increase the dosage of bca, gca, and pca in the defined L-lysine-producing strain C. glutamicum AHD-2 led to no discernable effects on growth and production. Northern blot analysis indicated that the bca transcript in strain AHD-2 and another L-lysine producer, C. glutamicum B-6, was present at a much higher level than in the wild-type strain, particularly during exponential growth phases. These results indicate that: (1) the bca product is essential to achieving normal growth under ordinary atmospheric conditions, and this effect is most likely due to the bca product's ability to maintain favorable intracellular bicarbonate/CO(2) levels, and (2) the expression of bca is induced during exponential growth phases and also in the case of L-lysine overproduction, both of which are conditions of higher bicarbonate demand.
碳酸酐酶催化二氧化碳和碳酸氢根的相互转化。我们将重点研究氨基酸生产菌谷氨酸棒杆菌中的这种酶,以评估碳酸氢根对于该菌生长所必需的羧化反应以及L - 赖氨酸过量生产所需羧化反应的可用性。全基因组序列分析表明,谷氨酸棒杆菌中有两个基因分别编码假定的β型和γ型碳酸酐酶。这些基因编码的多肽含有在每种类型碳酸酐酶中严格保守的锌配体,分别被命名为bca和gca。染色体bca基因的内部缺失导致该菌在大气条件(0.04% CO₂)下,在完全培养基和基本培养基上生长严重受阻。在升高的CO₂条件(5% CO₂)下,Δbca菌株的生长缺陷得以恢复。导入红藻紫球藻碳酸酐酶基因(pca)能够弥补bca基因的缺失,使该菌在大气CO₂水平下正常生长。相比之下,无论CO₂条件如何,Δgca菌株在生长方面的表现与野生型菌株相同。在限定的L - 赖氨酸生产菌株谷氨酸棒杆菌AHD - 2中增加bca、gca和pca的剂量,对生长和产量均未产生明显影响。Northern印迹分析表明,在菌株AHD - 2和另一个L - 赖氨酸生产菌谷氨酸棒杆菌B - 6中,bca转录本的水平比野生型菌株高得多,尤其是在指数生长阶段。这些结果表明:(1)bca产物对于在普通大气条件下实现正常生长至关重要,这种作用很可能归因于bca产物维持细胞内有利的碳酸氢根/CO₂水平的能力;(2)bca的表达在指数生长阶段以及L - 赖氨酸过量生产时被诱导,这两种情况都是对碳酸氢根需求较高的条件。