Biochemical Properties of Carbohydrate-Active Enzymes Synthesized by Penicillium chrysogenum Using Corn Straw as Carbon Source

2019 ◽  
Vol 11 (6) ◽  
pp. 2455-2466 ◽  
Author(s):  
Luísa de M. B. Silva ◽  
Tainah C. Gomes ◽  
Sadia F. Ullah ◽  
Alonso R. P. Ticona ◽  
Pedro R. V. Hamann ◽  
...  
2020 ◽  
Vol 23 (9) ◽  
pp. 312-318
Author(s):  
Martha Sari ◽  
Dirayanti Dirayanti ◽  
Eris Septiana ◽  
Bustanussalam Bustanussalam ◽  
Apon Zaenal Mustopa

The nutrition factor governs the growth and production of Penicillin G (Pen G) by Penicillium chrysogenum in a broth medium. Proper nutrition can improve Pen G antibiotic production. In this research, the optimal condition for Pen G production from P. chrysogenum in a standard culture medium and various carbon sources medium (glucose, lactose, maltose, and sucrose) were done for ten days. Phenylacetic Acid (PAA) precursor at 0.0 – 0.6 gL-1 (increment 0.1) was used to improve Pen G production. The Pen G was detected by HPLC, compared with the standard (Penicillin G Sodium Salt). The results showed that the PDB standard medium and lactose medium (150 rpm, at 30°C) produced 0.425 gL-1 and 0.107 gL-1 Pen G. Addition of 0.6 gL-1 PAA improved the Pen G production up to 0.045 gL-1 in the PDB medium, become the final concentration of 0.470 gL-1 and 2.460 gL-1 in the lactose medium, become the final concentration of 2.565 gL-1. The antibiotic’s activity against the pathogenic bacteria, i.e., B. subtilis, S. aureus, and S. typhi employing the disk diffusion method, has been done. The TLC method’s detection of the potential Pen G spots was conducted with ethyl acetate: distilled water: acetic acid (60:20:20) as the mobile phase. The Pen G extracts could inhibit the growth of all tested bacteria in Rf 0.65. This study informs the proper combination of carbon source and precursor effects and increases the bioproduction of Pen G from P. chrysogenum.


2008 ◽  
Vol 417 (2) ◽  
pp. 467-476 ◽  
Author(s):  
Martijn J. Koetsier ◽  
Peter A. Jekel ◽  
Marco A. van den Berg ◽  
Roel A. L. Bovenberg ◽  
Dick B. Janssen

Enzymatic activation of PAA (phenylacetic acid) to phenylacetyl-CoA is an important step in the biosynthesis of the β-lactam antibiotic penicillin G by the fungus Penicillium chrysogenum. CoA esters of PAA and POA (phenoxyacetic acid) act as acyl donors in the exchange of the aminoadipyl side chain of isopenicillin N to produce penicillin G or penicillin V. The phl gene, encoding a PCL (phenylacetate–CoA ligase), was cloned in Escherichia coli as a maltose-binding protein fusion and the biochemical properties of the enzyme were characterized. The recombinant fusion protein converted PAA into phenylacetyl-CoA in an ATP- and magnesium-dependent reaction. PCL could also activate POA, but the catalytic efficiency of the enzyme was rather low with kcat/Km values of 0.23±0.06 and 7.8±1.2 mM−1·s−1 for PAA and POA respectively. Surprisingly, PCL was very efficient in catalysing the conversion of trans-cinnamic acids to the corresponding CoA thioesters [kcat/Km=(3.1±0.4)×102 mM−1·s−1 for trans-cinnamic acid]. Of all the substrates screened, medium-chain fatty acids, which also occur as the side chains of the natural penicillins F, DF, H and K, were the best substrates for PCL. The high preference for fatty acids could be explained by a homology model of PCL that was constructed on the basis of sequence similarity with the Japanese firefly luciferase. The results suggest that PCL has evolved from a fatty-acid-activating ancestral enzyme that may have been involved in the β-oxidation of fatty acids.


2011 ◽  
Vol 347-353 ◽  
pp. 48-51 ◽  
Author(s):  
Shao Lan Zou ◽  
Chao Zhang ◽  
Yuan Yuan Ma ◽  
Le You ◽  
Min Hua Zhang

The recombinant Z.mobilis CX was constructed. Its ethanol concentration and ethanol yield from 2% xylose at 36 h were 6.73 g/L and 82.3% of theoretical yield, respectively. The recombinant S.cerevisiae YB was constructed and was showed to utilize cellobiose as the sole carbon source for rapid growth and ethanol production. The maximum ethanol concentration 7.493 g/L and ethanol yield 77.4% of theoretical yield from 2% cellobiose were obtained at 24 h. Further, the preliminary results of SSF of pretreated corn straw demonstrated the potential of improving ethanol production and reducing the costs of cellose enzymes used by co-fermentation of CX and YB.


2018 ◽  
Vol 33 ◽  
pp. 39-45 ◽  
Author(s):  
Cárol Cabral Terrone ◽  
Caroline de Freitas ◽  
César Rafael Fanchini Terrasan ◽  
Alex Fernando de Almeida ◽  
Eleonora Cano Carmona

2004 ◽  
Vol 39 (12) ◽  
pp. 1931-1938 ◽  
Author(s):  
Sarah de Vargas Andrade ◽  
Maria de Lourdes Teixeira de Moraes Polizeli ◽  
Héctor Francisco Terenzi ◽  
João Atı́lio Jorge

2015 ◽  
Vol 77 (31) ◽  
Author(s):  
Laila Muftah Zargoun ◽  
Nor Azimah Mohd Zain ◽  
Shafinaz Shahir

In this study, a polyhydroxybutyrate (PHB) producing bacterium was isolated from waste cooking oil and characterized for its morphological and biochemical properties. Staining methods utilizing Sudan Black B and Nile Blue A were used on isolated bacterium to demonstrate good capability for synthesizing PHB. It was shown that the isolated bacterium species was related to Bacillus thuringiensis LMA by using 16S rRNA gene sequences analysis. During the stationary phase, the Bacillus strain was subjected to 10 % (w/v) of pomegranate molasses as a carbon source and 5 g/L of peptone as a nitrogen source. 2 ml of batch fermentation was collected. Samples were collected twice during the incubation period for detection of PHB using Sudan Black B. The PHB production accounted for up to 57.45% of the cell dry weight. The PHB produced was characterized using Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance Spectroscopy (NMR). The drastic absorption band at approximately 1717 cm-1 indicated the stretching vibration of C=O group in PHB polyester, while the functional groups of PHB were identified methyl (-CH3) at 1.28 ppm, methylene (-CH2) 2.0 and 2.5 ppm, and methylene doublet group (CH3) at 5.3 ppm.


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