Author/Authors :
Sharafi, Zeinab Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Barati, Mahmood Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Khoshayand, Mohammad Reza Department of Drug and Food Control - Faculty of Pharmacy - Tehran University of Medical Sciences, Tehran, Iran , Adrangi, Sina Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Among the two types of bacterial L-asparaginases, only type II enzymes have been used in
the treatment of acute lymphoblastic leukemia owing to their higher affinity for L-asparagine.
However, current screening media used for the isolation of L-asparaginase-producing
microorganisms do not discriminate between the two types of L-asparaginase. During an
optimization study conducted to increase L-asparaginase production by environmental
Halomonas isolates, it was noticed that the pattern of L-asparaginase production in response
to variations in glucose concentration varied between different isolates suggesting that they
differ in their ability to produce type II L-asparaginases, an observation that was confirmed by
further experiments. Bioinformatics analysis of available Halomonas whole genome sequences
revealed that indeed some species of this genus possess both L-asparaginase types while others
possess only type I enzymes. By comparing the growth pattern of these isolates on different
media, we propose that by omitting glucose, reducing the concentration of L-asparagine and
providing an alternative nitrogen source in L-asparaginase screening media it may be possible
to differentiate between type I and type II activities.
Keywords :
Optimization , Oligotrophy , Halomonas , L-asparaginase , Screening