首页> 美国卫生研究院文献>International Scholarly Research Notices >Use of Nonspecific Glutamic Acid-Free Media and High Glycerol or High Amylase as Inducing Parameters for Screening Bacillus Isolates Having High Yield of Polyglutamic Acid
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Use of Nonspecific Glutamic Acid-Free Media and High Glycerol or High Amylase as Inducing Parameters for Screening Bacillus Isolates Having High Yield of Polyglutamic Acid

机译:使用非特异性无谷氨酸的培养基和高甘油或高淀粉酶作为诱导参数筛选具有高产率的聚谷氨酸芽孢杆菌分离物

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摘要

Out of fifty-five Bacillus isolates obtained from ten different regional locations and sources, seven showed the ability to consistently produce specific extracellular polymeric substance (EPS) on rich as well as synthetic but nonspecific media which did not contain glutamic acid. The isolates were identified as either Bacillus licheniformis or Bacillus subtilis. The EPS from all isolates was resistant to alpha protease, proteinase K, and was thus of high molecular weight. Further it was detected after SDS-PAGE by methylene blue but not by coomassie blue R staining as in case of proteins with high proportion of acidic amino acids. Cell-free EPS, after acid hydrolysis, showed absence of carbohydrates and presence of only glutamic acid. Thus the native the EPS from all seven isolates was confirmed to be gamma polyglutamic acid (PGA) and not exopolysaccharide. The Bacillus isolate T which produced maximum polymer on all media tested had higher amylase: protease activity as compared to other strains. If inoculum was developed in rich medium as compared to synthetic medium, the PGA produced increased by twofold in the subsequent synthetic production medium. Similarly, use of inoculum consisting of young and vegetative cells also increased the PGA production by twofold though amount of inoculum did not affect yield of PGA. Though PGA was produced in even in the absence of glutamic acid supplementation in the production medium by all isolates, the yield of PGA increased by fourfold in the presence glutamic acid and the maximum yield was 30 g/l for isolate K. The supplementation of glutamine instead of glutamic acid into the medium caused an increase in the viscosity of the non-Newtonian solution of PGA.
机译:从十个不同地区和来源获得的五十五种芽孢杆菌分离物中,有七种表现出能够在富含谷氨酸的合成以及非特异性培养基上连续产生特定的细胞外聚合物质(EPS)的能力。分离物被鉴定为地衣芽孢杆菌或枯草芽孢杆菌。来自所有分离物的EPS对α蛋白酶,蛋白酶K具有抗性,因此具有高分子量。此外,在SDS-PAGE后,通过亚甲基蓝检测到它,而不是通过考马斯亮蓝R染色检测到,如酸性氨基酸比例高的蛋白一样。酸水解后的无细胞EPS显示不存在碳水化合物,仅存在谷氨酸。因此,证实来自所有七个分离株的天然EPS是γ聚谷氨酸(PGA)而不是胞外多糖。与其他菌株相比,在所有测试培养基上产生最大聚合物的芽孢杆菌分离物T具有更高的淀粉酶:蛋白酶活性。如果与合成培养基相比,接种物是在丰富的培养基中培养的,则在随后的合成生产培养基中产生的PGA会增加两倍。同样,使用接种物组成的幼小和营养细胞也可将PGA产量提高两倍,尽管接种量不会影响PGA的产量。尽管所有分离株甚至在生产培养基中都不添加谷氨酸的情况下也生产PGA,但是在存在谷氨酸的情况下PGA的产量增加了四倍,分离株K的最大产量为30 g / l。补充谷氨酰胺代替谷氨酸进入培养基会导致PGA的非牛顿溶液的粘度增加。

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