Furuichi Keisuke, Hojo Ken-ichi, Katakura Yoshio, Ninomiya Kazuaki, Shioya Suteaki
Food Technology Research Institute, Meiji Dairies Corporation, 540 Naruda, Odawara, Kanagawa 250-0862, Japan.
J Biosci Bioeng. 2006 Jun;101(6):464-70. doi: 10.1263/jbb.101.464.
This is the first report on the production of both 1,4-dihydroxy-2-naphthoic acid (DHNA) and menaquinone by Propionibacterium freudenreichii ET-3. DHNA can be a stimulator of bifidogenic growth, and menaquinone has important roles in blood coagulation and bone metabolism. During anaerobic culture, DHNA and menaquinone concentrations reached 0.18 mM and 0.12 mM, respectively. The molar ratio between these products was approximately 3:2, which was not affected by culture pH and temperature over the ranges of 6.0-7.0 and 31-35 degrees C, respectively. As for organic acid, propionate and acetate accumulated at concentrations of 0.3 M and 0.15 M, respectively, and the propionate accumulation particularly inhibited further production of DHNA. To improve DHNA production, we switched from anaerobic condition to aerobic condition during the culture when lactose was depleted. DHNA concentration continued to increase even after lactose exhaustion, reaching 0.24 mM. In contrast to DHNA production, menaquinone production stopped after the switch to aerobic condition. The total molar production of DHNA and menaquinone was 0.3 mM irrespective of aerobic culture and anaerobic-aerobic switching culture. Therefore, the anaerobic-aerobic switching culture could increase the production ratio of DHNA to menaquinone. The DHNA concentration obtained from the anaerobic-aerobic switching culture was 1.3-fold higher than that in the anaerobic culture, because P. freudenreichii ET-3 utilized propionate accumulated in the medium via the reversed methylmalonyl CoA pathway under aerobic condition. The culture method proposed in this study could be applicable to industrial-scale fermentation using 1000 l of media, by which 0.23 mM DHNA was produced.
这是关于费氏丙酸杆菌ET-3生产1,4-二羟基-2-萘甲酸(DHNA)和甲萘醌的首篇报道。DHNA可以刺激双歧杆菌生长,而甲萘醌在血液凝固和骨骼代谢中发挥着重要作用。在厌氧培养过程中,DHNA和甲萘醌的浓度分别达到了0.18 mM和0.12 mM。这两种产物之间的摩尔比约为3:2,分别在6.0 - 7.0的pH范围和31 - 35摄氏度的温度范围内不受培养pH值和温度的影响。至于有机酸,丙酸和乙酸分别以0.3 M和0.15 M的浓度积累,丙酸的积累尤其抑制了DHNA的进一步产生。为了提高DHNA的产量,我们在培养过程中当乳糖耗尽时从厌氧条件切换到好氧条件。即使在乳糖耗尽后,DHNA浓度仍持续增加,达到了0.24 mM。与DHNA的产生不同,切换到好氧条件后甲萘醌的产生停止。无论好氧培养还是厌氧-好氧切换培养,DHNA和甲萘醌的总摩尔产量均为0.3 mM。因此,厌氧-好氧切换培养可以提高DHNA与甲萘醌的产量比。从厌氧-好氧切换培养中获得的DHNA浓度比厌氧培养中的高1.3倍,因为费氏丙酸杆菌ET-3在好氧条件下通过逆向甲基丙二酰辅酶A途径利用培养基中积累的丙酸。本研究中提出的培养方法可应用于使用1000升培养基的工业规模发酵,通过该方法可产生0.23 mM的DHNA。