Hong Seung-Hye, Ngo Ho-Phuong-Thuy, Nam Hyun-Koo, Kim Kyoung-Rok, Kang Lin-Woo, Oh Deok-Kun
Department of Bioscience and Biotechnology, Konkuk University, Seoul, South Korea.
Department of Biological Sciences, Konkuk University, Seoul, South Korea.
Appl Environ Microbiol. 2016 Jun 13;82(13):3940-3946. doi: 10.1128/AEM.00848-16. Print 2016 Jul 1.
A novel bacterial aldehyde dehydrogenase (ALDH) that converts retinal to retinoic acid was first identified in Bacillus cereus The amino acid sequence of ALDH from B. cereus (BcALDH) was more closely related to mammalian ALDHs than to bacterial ALDHs. This enzyme converted not only small aldehydes to carboxylic acids but also the large aldehyde all-trans-retinal to all-trans-retinoic acid with NAD(P)(+) We newly found that BcALDH and human ALDH (ALDH1A1) could reduce all-trans-retinal to all-trans-retinol with NADPH. The catalytic residues in BcALDH were Glu266 and Cys300, and the cofactor-binding residues were Glu194 and Glu457. The E266A and C300A variants showed no oxidation activity. The E194S and E457V variants showed 15- and 7.5-fold higher catalytic efficiency (kcat/Km) for the reduction of all-trans-retinal than the wild-type enzyme, respectively. The wild-type, E194S variant, and E457V variant enzymes with NAD(+) converted 400 μM all-trans-retinal to 210 μM all-trans-retinoic acid at the same amount for 240 min, while with NADPH, they converted 400 μM all-trans-retinal to 20, 90, and 40 μM all-trans-retinol, respectively. These results indicate that BcALDH and its variants are efficient biocatalysts not only in the conversion of retinal to retinoic acid but also in its conversion to retinol with a cofactor switch and that retinol production can be increased by the variant enzymes. Therefore, BcALDH is a novel bacterial enzyme for the alternative production of retinoic acid and retinol.
Although mammalian ALDHs have catalyzed the conversion of retinal to retinoic acid with NAD(P)(+) as a cofactor, a bacterial ALDH involved in the conversion is first characterized. The biotransformation of all-trans-retinal to all-trans-retinoic acid by BcALDH and human ALDH was altered to the biotransformation to all-trans-retinol by a cofactor switch using NADPH. Moreover, the production of all-trans-retinal to all-trans-retinol was changed by mutations at positions 194 and 457 in BcALDH. The alternative biotransformation of retinoids was first performed in the present study. These results will contribute to the biotechnological production of retinoids, including retinoic acid and retinol.
一种将视黄醛转化为视黄酸的新型细菌醛脱氢酶(ALDH)最初是在蜡样芽孢杆菌中鉴定出来的。蜡样芽孢杆菌的ALDH(BcALDH)的氨基酸序列与哺乳动物的ALDH更为相似,而与细菌的ALDH差异较大。这种酶不仅能将小分子醛转化为羧酸,还能利用NAD(P)(+)将大分子醛全反式视黄醛转化为全反式视黄酸。我们新发现,BcALDH和人ALDH(ALDH1A1)可以利用NADPH将全反式视黄醛还原为全反式视黄醇。BcALDH中的催化残基是Glu266和Cys300,辅因子结合残基是Glu194和Glu457。E266A和C300A变体没有氧化活性。E194S和E457V变体在还原全反式视黄醛时的催化效率(kcat/Km)分别比野生型酶高15倍和7.5倍。野生型、E194S变体和E457V变体酶在使用NAD(+)时,在240分钟内将400μM全反式视黄醛等量转化为210μM全反式视黄酸,而在使用NADPH时,它们分别将400μM全反式视黄醛转化为20、90和40μM全反式视黄醇。这些结果表明,BcALDH及其变体不仅是将视黄醛转化为视黄酸的高效生物催化剂,而且通过辅因子转换将其转化为视黄醇也是高效的,并且变体酶可以提高视黄醇的产量。因此,BcALDH是一种用于视黄酸和视黄醇替代生产的新型细菌酶。
尽管哺乳动物的ALDHs以NAD(P)(+)为辅因子催化视黄醛向视黄酸的转化,但首次鉴定出了一种参与该转化的细菌ALDH。通过使用NADPH进行辅因子转换,BcALDH和人ALDH将全反式视黄醛向全反式视黄酸的生物转化改变为向全反式视黄醇的生物转化。此外,BcALDH中第194和457位的突变改变了全反式视黄醛向全反式视黄醇的生成。本研究首次进行了类视黄醇替代生物转化。这些结果将有助于类视黄醇(包括视黄酸和视黄醇)的生物技术生产。