Abdulkarim Sabo Mohammed

Prof. Abdulkarim Sabo Mohammed


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
Verified
Journal Article
Open access
PDF file
MZMohsen Zareian
Mohsen Zareian
AEAfshin Ebrahimpour
Afshin Ebrahimpour
FBFatimah Abu Bakar
Fatimah Abu Bakar
AMAbdulkarim Sabo Mohammed
Abdulkarim Sabo Mohammed
BFBita Forghani
Bita Forghani
NSNazamid Saari
Nazamid Saari
L-glutamaic acid is the principal excitatory neurotransmitter in the brain and an important intermediate in metabolism. In the present study, lactic acid bacteria (218) were isolated from six different fermented foods as potent sources of glutamic acid producers. The presumptive bacteria were tested for their ability to synthesize glutamic acid. Out of the 35 strains showing this capability, strain MNZ was determined as the highest glutamic-acid producer. Identification tests including 16S rRNA gene sequencing and sugar assimilation ability identified the strain MNZ as Lactobacillus plantarum. The characteristics of this microorganism related to its glutamic acid-producing ability, growth rate, glucose consumption and pH profile were studied. Results revealed that glutamic acid was formed inside the cell and excreted into the extracellular medium. Glutamic acid production was found to be growth-associated and glucose significantly enhanced glutamic acid production (1.032 mmol/L) compared to other carbon sources. A concentration of 0.7% ammonium nitrate as a nitrogen source effectively enhanced glutamic acid production. To the best of our knowledge this is the first report of glutamic acid production by lactic acid bacteria. The results of this study can be further applied for developing functional foods enriched in glutamic acid and subsequently γ-amino butyric acid (GABA) as a bioactive compound.

1 September 2014 in Food Chemistry
Verified
Journal Article
Closed access
ODOmar Dahimi
Omar Dahimi
ARAlina Abdul Rahim
Alina Abdul Rahim
AMAbdulkarim Sabo Mohammed
Abdulkarim Sabo Mohammed
MHMohd Sukri Hassan
Mohd Sukri Hassan
SHShazamawati B.T. Zam Hashari
Shazamawati B.T. Zam Hashari
SSSami Saadi
Sami Saadi

1 January 2012 in The Scientific World Journal
Verified
Journal Article
Open access
PDF file
KUKabir Mustapha Umar
Kabir Mustapha Umar
AMAbdulkarim Sabo Mohammed
Abdulkarim Sabo Mohammed
SRSon Radu
Son Radu
AHAzizah Abdul Hamid
Azizah Abdul Hamid
NSNazamid Saari
Nazamid Saari
A mimicked biosynthetic pathway of catechin metabolite genes fromC. sinensis, consisting of flavanone 3 hydroxylase (F3H), dihydroflavonol reductase (DFR), and leucoanthocyanidin reductase (LCR), was designed and arranged in two sets of constructs: (a) single promoter in front of F3H and ribosome-binding sequences both in front of DFR and LCR; (b) three different promoters with each in the front of the three genes and ribosome-binding sequences at appropriate positions. RecombinantE. coliBL (DE3) harbouring the constructs were cultivated for 65 h at 26°C in M9 medium consisting of 40 g/L glucose, 1 mM IPTG, and 3 mM eriodictyol. Compounds produced were extracted in ethyl acetate in alkaline conditions after 1 h at room temperature and identified by HPLC. Two of the four major catechins, namely, (−)-epicatechin (0.01 ) and (−)-epicatechin gallate (0.36 mg/L), and two other types ((+)-catechin hydrate (0.13 mg/L) and (−)-catechin gallate (0.04 mg/L)) were successfully produced.