Yeast Strain Development for Extracellular Enzyme Production

2020 ◽  
pp. 185-223
Author(s):  
Malcolm A. J. Finkelman
2021 ◽  
Vol 47 (2) ◽  
pp. 306-316
Author(s):  
O.C. Amadi ◽  
C.C. Mbaeke ◽  
T.N. Nwagu ◽  
C.I. Nnamchi ◽  
I.A. Ndubuisi ◽  
...  

Renewable plant wastes constitute environmental nuisance. Their conversion by enzymes into bioethanol can be beneficial. We investigated the use of renewable plant waste as substrate for enzyme production and hydrolysis of the plant waste for ethanol production using an indigenous yeast strain. Five yeast strains; MCC-1, MCC-2, MCC-3, MCC-4 and MCC-5 were evaluated for production of sugars, α-amylase, glucoamylase and bioethanol using soluble starch. Phylogenetic analysis using partial sequence of the ITS gene classified MCC-4 as Pichia exigua. Proximate composition of plant wastes – cassava, wild yam, mango seed, udara seed and breadfruit were determined. Results showed total carbohydrate of (83.9%) for cassava flour. The ability of yeast to utilize these substrates and the effect of culture conditions (inoculum, pH, nitrogen source and substrate concentration) were also determined. Cassava pulp flour was the best substrate producing reducing sugar (1.471 ± 0.056mg/mL), α-amylase (0.573 ± 0.019U/mL), glucoamylase (1.605 ± 0.119U/mL), and ethanol (4.440 ± 0.014g/L). Culture conditions revealed optimum for inoculum concentration as (1mL), pH (4), nitrogen source (soya bean, 3g/L) and substrate concentration of (8%). Pichia exigua (MCC-4) a natural yeast strain isolated from the soil has the potential for both enzyme and ethanol production in a single step process.


1972 ◽  
Vol 50 (8) ◽  
pp. 1743-1748 ◽  
Author(s):  
Douglas P. Maxwell ◽  
Paul H. Williams ◽  
Martha D. Maxwell

The possible functional role of vesicles and crystal-containing microbodies in the production of oxalate, endopolygalacturonase, or cellulase by Sclerotinia sclerotiorum was investigated. The presence of multivesicular bodies in hyphal tips was not correlated with secretion or production of oxalate or these extracellular hydrolases. More crystal-containing microbodies were present in hyphal tips grown on media which supported greater extracellular enzyme production. No correlation existed between numbers of crystal-containing microbodies in hyphal tips and production of oxalate. Numerous membrane-bound vesicles (0.09–0.18 µm diam) were associated with tips grown on a D-glucose–Na succinate medium which supported high production of oxalate. The general ultrastructural organization of these hyphal tips was similar to that reported for other ascomycetes. Differences in numbers and distributions of organelles were observed between hyphal tips and older hyphae as well as between hyphal tips grown on the different carbon sources.


2019 ◽  
Vol 77 (1) ◽  
pp. 49-54 ◽  
Author(s):  
Yunjun Pan ◽  
Liwei Gao ◽  
Xiujun Zhang ◽  
Yuqi Qin ◽  
Guodong Liu ◽  
...  

1990 ◽  
Vol 36 (9) ◽  
pp. 617-624 ◽  
Author(s):  
Saswati Sengupta ◽  
S. Sengupta

Termitomyces clypeatus constitutively liberated amyloglucosidase; the liberation was not repressed by glucose. Growth of the mushroom in synthetic medium was slow with starch, and only amyloglucosidase was liberated. Yeast extract stimulated growth and enzyme production in starch medium, and α-amylase along with amyloglucosidase was detected extracellularly. The mushroom could not utilise cellulose or liberate endo-β(1 → 4)-glucanase even when inducer cellobiose or glucose was added to cellulose at different concentrations. Cellobiose alone also failed to induce any extracellular endo-β(1 → 4)-glucanase production. Yeast extract in both cellulose and cellobiose media supported liberation of endo-β(1 → 4)-glucanase. Lactose was found to be a poor inducer even in yeast extract medium. However, both α-amylase and endo-β(1 → 4)-glucanase were detected intracellularly at a basal level even when the enzymes were absent extracellularly under inducing and noninducing conditions. The intracellular enzymes were only freely liberated into the medium in the presence of yeast extract. It appeared that induction of α-amylase and endo-β(1 → 4)-glucanase was largely inhibited by the restricted liberation of the enzymes in absence of yeast extract. Of the yeast extract components, amino acids were the active ingredient mimicking the role of yeast extract in induction. Yeast extract was found to relieve catabolic inhibition observed at the late phase of enzyme production. It is proposed that catabolic inhibition might have a role in the enzyme liberation and that amino acids supported extracellular enzyme production by relieving this inhibition. Key words: mushroom, Termitomyces clypeatus, catabolic inhibition, polysaccharidase induction, amino acid.


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