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L-山梨糖发酵产生维生素C前体——2-酮基-L-古龙酸的研究 Ⅱ.发酵条件的研究
STUDIES ON PRODUCTION OF VITAMIN C PRECURSOR——2-KETO-L-GULONIC ACID FROM L-SORBOSE BY FERMENTATION Ⅱ. CONDITIONS FOR SUBMERGED FERMENTATION OF 2-KETO-L-GULONIC ACID
【摘要】 <正> 对产生维生素C前体2-酮基-L-古龙酸的优良菌株N1197A,进行了一系列摇并条件试验。添加玉米浆及尿素是提高产酸的有效手段,尿素浓度以0.5—0.8%为好,确定了培养基组成(%)为:K2HPO4 0.07、KH2PO4 0.03,甘油0.2,MgSO4·7H2O 0.01,轻体CaCO3 0.5,玉米浆0.5,尿素0.5,自来水配制,自然pH。在碳酸钙添加试验中,当培养基中有尿素时,不加碳酸钙与加碳酸钙产酸量相同。分批补加尿素或(NH4)2HPO4使发酵液pH保持在6—6.5,产酸量随着补加次数加多而增加。在发酵过程中,补加尿素调节发酵液pH是本发酵的特点。培养基中山梨糖浓度为7%,产酸稳定在30毫克/毫升,转化率39.7%。增加山梨糖浓度至10%,并增加尿素用量,产酸可达37毫克/毫升,转化率34.3%。本文中提到了N1197A是含有菌落大小不同的两种菌的混合菌株,只有当两者同时存在时,才能顺利进行由L-山梨糖转化成2-酮基-L-古龙酸这一生物氧化过程。
【Abstract】 The fermentation of vitamin C precursor 2-keto-L-gulonic acid (2-KGA) with strain N1197A was studied extensively. The data obtained showed that the addition of corn steep liquor and urea increased the 2-KGA yield significantly. The concentration of urea ranging from 0.5—0.8% was optimal. The constituents of the medium in percentage were as follows: Lsorbose 7, K2HPO4 0.07, KH2PO4 0.03, glycerin 0.2, MgSO4, 7H2O 0.01, CaCO3 0.5, corn steep liquor 0.5, urea 0.5, tap water, natural pH. When the medium contained urea, CaCO3 was not necessary as a pH regulator. Periodical feeding of urea or (NH4)2 HPO4 during fermentation resulted in maintenance of pH in the range of 6—6.5, and an increase of 2-KGA.When the medium contained 7% Lsorbose, the yield of 2-KGA was kept at 30 mg/ml and the rate of conversion was 39.7%. The requirement of urea was in parallel with concentration of L-sorbose. In a 10% L-sorbose medium with adequate concentration of urea, the rate of conversion reached 34.3% and the 2-KGA yield was 37 mg/ml.The present paper showed that strain N1197A actually is a mixed population consisting of small and big colony formers. The small one produces trace amount of 2-KGA when growing alone and the biger one produces nothing at all. Only when both kinds co-existed the process of converting L-sorbose into 2-KGA can be carried out in large quantities successfully.
- 【文献出处】 微生物学报 ,Acta Microbiologica Sinica , 编辑部邮箱 ,1981年02期
- 【被引频次】34
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