Selim M H, Elshikh H H, El-Hadedy D E, Saad M M, Eliwa E, Abdelraof M
Microbial Chemistry Dep., National Research Center (NRC), Giza, Egypt.
Botany and Microbiology Dep., Faculty of Science (Boys), Al-Azhar University, Cairo, Egypt.
J Genet Eng Biotechnol. 2015 Dec;13(2):129-137. doi: 10.1016/j.jgeb.2015.08.001. Epub 2015 Sep 11.
Among 60 isolates of tested; only 40 isolates were capable to utilize l-methionine as the only source of nitrogen in medium. In addition, 24 of these isolates could grow in medium amended with l-methionine as a source of nitrogen and carbon. Qualitative rapid plate assay test shows the ability of 18 of these isolates to grow with a pink color surrounding their colonial growth, while 6 of these isolates could grow and utilize l-methionine without any pink color around their colonial growth. Quantitative assay test shows the rate of l-methioninase production by all isolates tested. Permeabilization treatment including chemical and physical methods proved that l-methioninase was found to be extracellularly produced. The results also indicate that l-methioninase production was not correlated with growth rate or l-methionine consumption in medium. On the other hand, quantitative assay test shows that these six isolates were l-methioninase negative and failed to produce any amount of l-methioninase. In addition, results also show that isolates No. 4 and No. 60 were the most suitable for l-methioninase production, these two isolates were characterized and identified as sp. DMMMH 4 and sp. MDMMH 60 using 16S rRNA with accession No. in gene bank. Furthermore, optimal conditions for enzyme activity produced by the two isolates were established in relation to temperature, pH, reaction time and type of buffer used and its molarities.
在测试的60株菌株中,只有40株能够利用L-甲硫氨酸作为培养基中唯一的氮源。此外,这些菌株中有24株能够在添加L-甲硫氨酸作为氮源和碳源的培养基中生长。定性快速平板试验表明,其中18株菌株在菌落生长周围有粉红色区域时能够生长,而其中6株菌株能够生长并利用L-甲硫氨酸,但其菌落生长周围没有任何粉红色。定量试验显示了所有测试菌株产生L-甲硫氨酸酶的速率。包括化学和物理方法的透化处理证明L-甲硫氨酸酶是细胞外产生的。结果还表明,L-甲硫氨酸酶的产生与培养基中的生长速率或L-甲硫氨酸消耗无关。另一方面,定量试验表明这6株菌株为L-甲硫氨酸酶阴性,未能产生任何量的L-甲硫氨酸酶。此外,结果还表明,4号和60号菌株最适合产生L-甲硫氨酸酶,使用基因库中登录号为的16S rRNA将这两株菌株鉴定为DMMMH 4菌和MDMMH 60菌。此外,还确定了这两株菌株产生的酶活性在温度、pH、反应时间、所用缓冲液类型及其摩尔浓度方面的最佳条件。