Syldatk C, Mackowiak V, Höke H, Gross C, Dombach G, Wagner F
Institute of Biochemistry and Biotechnology A, Technical University of Braunschweig, F.R.G.
J Biotechnol. 1990 Jun;14(3-4):345-61. doi: 10.1016/0168-1656(90)90118-u.
A microorganism with the ability to form L-tryptophan from D,L-5-(3-indolyl-methyl)hydantoin (D,L-5-IMH) was isolated and identified as Arthrobacter sp. (DSM 3747). After isolation of a mutant with high tryptophan production activity but low tryptophan degradation, cultural conditions were optimized to achieve high amounts of biomass with good specific activities concerning the enzymatic hydantoin-cleaving reactions. The ability of the microorganism to perform these bioconversions was found to be inducible by D,L-5-IMH as well as to be dependent on the presence of Mn2+. The highest specific D,L-5-IMH-cleaving activity of the cells was observed in the exponential phase of growth. The addition of yeast extract to the mineral salts medium was found to be essential for obtaining biomass concentrations of about 25 g l-1 cell dry mass by bioreactor cultivations. In order to obtain a constantly high growth rate, feeding of the C-source was pO2-controlled. The inducer D,L-5-IMH had to be continuously fed to prevent a decline of the L-tryptophan-forming enzyme activities, because it was subjected to degradation with the enzymes induced and higher concentrations of D,L-5-IMH aggravated the growth significantly. The synthesis of the enzymes was also inducible, when inducer and Mn2+ were not added until the late growth phase. Using this process, the consumption of D,L-5-IMH was reduced remarkably. So, under these conditions biomass concentrations of 25 g l-1 cell dry weight with a specific enzymatic activity of 0.20 mmol g-1 h-1 (tryptophan per dry mass per time) could be obtained within 13 h. Using 1 g l-1 of the chemically modified inducer D,L-5-(3-indolylmethyl)-3-N-methylhydantoin, which was not degradable by the microorganisms, a biomass concentration of 28 g l-1 cell dry weight with a specific activity of 0.34 mmol g-1 h-1 (tryptophan per dry mass per time) could be obtained within 28 h.
从D,L-5-(3-吲哚甲基)乙内酰脲(D,L-5-IMH)合成L-色氨酸的一种微生物被分离出来,并鉴定为节杆菌属(DSM 3747)。在分离出具有高色氨酸生产活性但色氨酸降解能力低的突变体后,优化了培养条件,以获得大量生物量,且这些生物量在乙内酰脲裂解酶促反应方面具有良好的比活性。发现该微生物进行这些生物转化的能力可被D,L-5-IMH诱导,并且依赖于Mn2+的存在。在生长指数期观察到细胞的最高比D,L-5-IMH裂解活性。发现向矿物盐培养基中添加酵母提取物对于通过生物反应器培养获得约25 g l-1细胞干重的生物量浓度至关重要。为了获得持续的高生长速率,碳源的进料采用pO2控制。诱导剂D,L-5-IMH必须持续进料以防止L-色氨酸形成酶活性下降,因为它会被诱导的酶降解,且较高浓度的D,L-5-IMH会显著加剧生长。当直到生长后期才添加诱导剂和Mn2+时,酶的合成也可被诱导。使用该方法,D,L-5-IMH的消耗量显著降低。因此,在这些条件下,13小时内可获得25 g l-1细胞干重的生物量浓度,比酶活性为0.20 mmol g-1 h-1(每单位时间每干重的色氨酸)。使用1 g l-1不可被微生物降解的化学修饰诱导剂D,L-5-(3-吲哚甲基)-3-N-甲基乙内酰脲,28小时内可获得28 g l-1细胞干重的生物量浓度,比活性为0.34 mmol g-1 h-1(每单位时间每干重的色氨酸)。