共查询到20条相似文献,搜索用时 15 毫秒
1.
N. Barron R. Marchant L. McHale A. P. McHale 《Applied microbiology and biotechnology》1995,43(3):518-520
The thermotolerant yeast strain, Kluyveromyces marxianus IMB3, was found to be capable of ethanol production during growth at 45°C on media containing milled paper and exogenously
added commercial cellulase. At maximum achievable cellulose concentrations in shake-flask cultures, ethanol production increased
to 6.6 g/l at 45°C, representing an overall level of conversion of 21% of the maximum theoretical yield. Subsequent studies
involving variations in added cellulase concentrations to the batch systems demonstrated that ethanol yields could be increased
to 10 g/l at 45°C, which represented 39% of the maximum theoretical yield. As a result of ethanol production at 45°C in the
systems examined, we suggest that the thermotolerant ethanol-producing yeast strain K. marxianus represents a novel candidate for use in simultaneous saccharification and conversion of the resulting substrates to ethanol.
Received: 9 June 1994/Received revision: 8 August 1994/Accepted: 12 August 1994 相似文献
2.
Takao Kitagawa Kenro Tokuhiro Hidehiko Sugiyama Katsuhiro Kohda Naoto Isono Makoto Hisamatsu Haruo Takahashi Takao Imaeda 《Applied microbiology and biotechnology》2010,87(5):1841-1853
We demonstrate the value of the thermotolerant yeast Issatchenkia orientalis as a candidate microorganism for bioethanol production from lignocellulosic biomass with the goal of consolidated bioprocessing.
The I. orientalis MF-121 strain is acid tolerant, ethanol tolerant, and thermotolerant, and is thus a multistress-tolerant yeast. To express
heterologous proteins in I. orientalis, we constructed a transformation system for the MF-121 strain and then isolated the promoters of TDH1 and PGK1, two genes that were found to be strongly expressed during ethanol fermentation. As a result, expression of β-glucosidase
from Aspergillus aculeatus could be achieved with I. orientalis, demonstrating successful heterologous gene expression in I. orientalis for the first time. The transformant could convert cellobiose to ethanol under acidic conditions and at high temperature.
Simultaneous saccharification and fermentation (SSF) was performed with the transformant, which produced 29 g l−1 of ethanol in 72 h at 40°C even without addition of β-glucosidase when SSF was carried out in medium containing 100 g l−1 of microcrystalline cellulose and a commercial cellulase preparation. These results suggest that using a genetically engineered
thermotolerant yeast such as I. orientalis in SSF could lead to cost reduction because less saccharification enzymes are required. 相似文献
3.
S A Shaikh J M Khire M I Khan 《Journal of industrial microbiology & biotechnology》1997,19(4):239-245
A thermostable β-galactosidase was produced extracellularly by a thermophilic Rhizomucor sp, with maximum enzyme activity (0.21 U mg−1) after 4 days under submerged fermentation condition (SmF). Solid state fermentation (SSF) resulted in a nine-fold increase
in enzyme activity (2.04 U mg−1). The temperature range for production of the enzyme was 38–55°C with maximum activity at 45°C. The optimum pH and temperature
for the partially purified enzyme was 4.5 and 60°C, respectively. The enzyme retained its original activity on incubation
at 60°C up to 1 h. Divalent cations like Co2+, Mn2+, Fe2+ and Zn2+ had strong inhibitory effects on the enzyme activity. The K
m and V
max for p-nitrophenyl-β- D-galactopyranoside and o-nitrophenyl-β - D-galactopyranoside were 0.39 mM, 0.785 mM and 232.1 mmol min−1 mg−1 respectively. The K
m and V
max for the natural substrate lactose were 66.66 μM and 0.20 μ mol min−1 mg−1.
Received 10 March 1997/ Accepted in revised form 17 July 1997 相似文献
4.
The thermotolerant fungus, Aspergillus niger NCIM 563, was used for production of extracellular phytase on agricultural residues: wheat bran, mustard cake, cowpea meal,
groundnut cake, coconut cake, cotton cake and black bean flour in solid state fermentation (SSF). Maximum enzyme activity
(108 U g−1 dry mouldy bran, DMB) was obtained with cowpea meal. During the fermentation phytic acid was hydrolysed completely with a
corresponding increase in biomass and phytase activity within 7 days. Phosphate in the form of KH2PO4 (10 mg per 100 g of agriculture residue) increased phytase activity. Among various surfactants added to SSF, Trition X-100
(0.5%) exhibited a 30% increase in phytase activity. The optimum pH and temperature of the crude enzyme were 5.0 and 50°C
respectively. Phytase activity (86%) was retained in buffer of pH 3.5 for 24 h. The enzyme retained 75% of its activity on
incubation at 55°C for 1 h. In the presence of 1 mM K+ and Zn2+, 95% and 55% of the activity were retained. Scanning electron microscopy showed a high density growth of fungal mycelia on
wheat bran particles during SSF. Journal of Industrial Microbiology & Biotechnology (2000) 24, 237–243.
Received 07 June 1999/ Accepted in revised form 18 December 1999 相似文献
5.
Continuous production of l(+)-lactic acid by Lactobacillus casei in two-stage systems 总被引:2,自引:0,他引:2
Bruno-Bárcena JM Ragout AL Córdoba PR Siñeriz F 《Applied microbiology and biotechnology》1999,51(3):316-324
A two-stage two-stream chemostat system and a two-stage two-stream immobilized upflow packed-bed reactor system were used
for the study of lactic acid production by Lactobacillus casei subsp casei. A mixing ratio of D
12/D
2 = 0.5 (D = dilution rate) resulted in optimum production, making it possible to generate continuously a broth with high lactic acid
concentration (48 g l−1) and with a lowered overall content of initial yeast extract (5 g l−1), half the concentration supplied in the one-step process. In the two-stage chemostat system, with the first stage at pH
5.5 and 37 °C and a second stage at pH 6.0, a temperature change from 40 °C to 45 °C in the second stage resulted in a 100%
substrate consumption at an overall dilution rate of 0.05 h−1. To increase the cell mass in the system, an adhesive strain of L. casei was used to inoculate two packed-bed reactors, which operated with two mixed feedstock streams at the optimal conditions
found above. Lactic acid fermentation started after a lag period of cell growth over foam glass particles. No significant
amount of free cells, compared with those adhering to the glass foam, was observed during continuous lactic acid production.
The extreme values, 57.5 g l−1 for lactic acid concentration and 9.72 g l−1 h−1 for the volumetric productivity, in upflow packed-bed reactors were higher than those obtained for free cells (48 g l−1 and 2.42 g l−1 h−1) respectively and the highest overall l(+)-lactic acid purity (96.8%) was obtained in the two-chemostat system as compared with the immobilized-cell reactors (93%).
Received: 4 December 1997 / Received revision: 23 February 1998 / Accepted: 14 March 1998 相似文献
6.
The biodegradation of tributyl phosphate (Bu3-P, TBP), releasing phosphate at a high enough concentration locally to precipitate uranium from solution, was demonstrated
by a mixed culture consisting primarily of pseudomonads. The effect of various parameters on Bu3-P biodegradation by growing cells is described. Growth at the expense of Bu3-P as the carbon and phosphorus source occurred over a pH range from 6.5 to 8, and optimally at pH 7. Bu3-P biodegradation was optimal at 30 °C, reduced at 20 °C and negligible at 4 °C and 37 °C. Incorporation of Cu or Cd inhibited,
and Ni, Co and Mn reduced its degradation. Inorganic phosphate (above 10 mM) and kerosene (up to 1 g/l) reduced Bu3-P biodegradation significantly, but nitrate had no effect. Sulphate (10–100 mM) was inhibitory. When pregrown biomass was used
the fastest rates of tributyl and dibutyl phosphate biodegradation were 25 μmol h−1 mg protein−1 and 37 μmol h−1 mg protein−1 respectively. Microcarrier-immobilised biomass decontaminated uranium-bearing acid mine waste water by uranium phosphate
precipitation at the expense of Bu3-P hydrolysis in the presence of 35 mM SO4
2−. At pH 4.5, 79% of the UO2
2+ was removed at a flow rate of 1.4 ml/h on a 7-ml test column.
Received: 2 June 1997 / Received revision: 15 September 1997 / Accepted: 19 September 1997 相似文献
7.
The influence of low temperature (5–29 °C) on the methanogenic activity of non-adapted digested sewage sludge and on temperature/leachate-adapted
biomass was assayed by using municipal landfill leachate, intermediates of anaerobic degradation (propionate) and methane
precursors (acetate, H2/CO2) as substrates. The temperature dependence of methanogenic activity could be described by Arrhenius-derived models. However,
both substrate and adaptation affected the temperature dependence. The adaptation of biomass in a leachate-fed upflow anaerobic
sludge-blanket reactor at approximately 20 °C for 4 months resulted in a sevenfold and fivefold increase of methanogenic activity
at 11 °C and 22 °C respectively. Both acetate and H2/CO2 were methanized even at 5 °C. At 22 °C, methanogenic activities (acetate 4.8–84 mM) were 1.6–5.2 times higher than those
at 11 °C. The half-velocity constant (K
s) of acetate utilization at 11 °C was one-third of that at 22 °C while a similar K
i was obtained at both temperatures. With propionate (1.1–5.5 mM) as substrate, meth‐anogenic activities at 11 °C were half
those at 22 °C. Furthermore, the residual concentration of the substrates was not dependent on temperature. The results suggest
that the adaptation of biomass enables the achievement of a high treatment capacity in the anaerobic process even under psychrophilic
conditions.
Received: 23 December 1996 / Received last revision: 18 June 1997 / Accepted: 23 June 1997 相似文献
8.
Nutrient cost is an important aspect in the fermentation of biomass to ethanol. With a goal of developing a cost-effective
fermentation medium, several industrially available nutrient sources were evaluated for their effectiveness in the simultaneous
saccharification and fermentation of pretreated poplar with Saccharomyces cerevisiae D5A. These studies showed that a low-cost medium containing 0.3% corn steep liquor and 2.5 mM MgSO4 · 7H2O was similar in performance to a nutrient-rich medium. Besides its low cost, this alternative medium consists of components
that are available on a commercial scale, thereby making it industrially relevant.
Received: 14 August 1996 / Received revision: 7 January 1997 / Accepted: 24 January 1997 相似文献
9.
Ethanol production by recombinant Escherichia coli strain FBR5 from dilute acid pretreated wheat straw (WS) by separate hydrolysis and fermentation (SHF) and simultaneous saccharification
and fermentation (SSF) was studied. The yield of total sugars from dilute acid (0.5% H2SO4) pretreated (160 °C, 10 min) and enzymatically saccharified (pH 5.0, 45 °C, 72 h) WS (86 g/l) was 50.0 ± 1.4 g/l. The hydrolyzate
contained 1,184 ± 19 mg furfural and 161 ± 1 mg hydroxymethyl furfural per liter. The recombinant E. coli FBR5 could not grow at all at pH controlled at 4.5 to 6.5 in the non-abated wheat straw hydrolyzate (WSH) at 35 °C. However,
it produced 21.9 ± 0.3 g ethanol from non-abated WSH (total sugars, 44.1 ± 0.4 g/l) in 90 h including the lag time of 24 h
at controlled pH 7.0 and 35 °C. The bioabatement of WS was performed by growing Coniochaeta ligniaria NRRL 30616 in the liquid portion of the pretreated WS aerobically at pH 6.5 and 30 °C for 15 h. The bacterium produced 21.6 ± 0.5 g
ethanol per liter in 40 h from the bioabated enzymatically saccharified WSH (total sugars, 44.1 ± 0.4 g) at pH 6.0. It produced
24.9 ± 0.3 g ethanol in 96 h and 26.7 ± 0.0 g ethanol in 72 h per liter from bioabated WSH by batch SSF and fed-batch SSF,
respectively. SSF offered a distinct advantage over SHF with respect to reducing total time required to produce ethanol from
the bioabated WS. Also, fed-batch SSF performed better than the batch SSF with respect to shortening the time requirement
and increase in ethanol yield. 相似文献
10.
A number of nutritional factors influencing growth and glucose oxidase (EC 1.1.3.4) production by a newly isolated strain
of Penicillium pinophilum were investigated. The most important factors for glucose oxidase production were the use of sucrose as the carbon source,
and growth of the fungus at non-optimal pH 6.5. The enzyme was purified to apparent homogeneity with a yield of 74%, including
an efficient extraction step of the mycelium mass at pH 3.0, cation-exchange chromatography and gel filtration. The relative
molecular mass (M
r) of native glucose oxidase was determined to be 154 700 ± 4970, and 77 700 for the denatured subunit. Electron-microscopic
examinations revealed a sandwich-shaped dimeric molecule with subunit dimensions of 5.0 × 8.0 nm. Glucose oxidase is a glycoprotein
that contains tightly bound FAD with an estimated stoichiometry of 1.76 mol/mol enzyme. The enzyme is specific for d-glucose, for which a K
m value of 6.2 mM was determined. The pH optimum was determined in the range pH 4.0–6.0. Glucose oxidase showed high stability
on storage in sodium citrate (pH 5.0) and in potassium phosphate (pH 6.0), each 100 mM. The half-life of the activity was
considerably more than 305 days at 4 °C and 30 °C, and 213 days at 40 °C. The enzyme was unstable at temperatures above 40 °C
in the range pH 2.0–4.0 and at a pH above 7.0.
Received: 18 November 1996 / Received revision: 3 March 1997 / Accepted: 7 March 1997 相似文献
11.
B. L. García A. S. Ball J. Rodríguez M. I. Pérez-Leblic M. E. Arias J. L. Copa-Patiño 《Applied microbiology and biotechnology》1998,50(2):213-218
Streptomyces avermitilis CECT 3339 produces extracellular ferulic acid esterase (FAE) activity during growth on a range of lignocellulose substrates.
Maximal levels of FAE activity were detected in culture filtrates from S. avermitilis CECT 3339 grown in media containing wheat bran and yeast extract as carbon and nitrogen sources respectively. Biochemical
characterization of this enzyme activity revealed that it was 100-fold higher when wheat bran was pretreated with Celluclast
(a mix of hydrolytic enzymes). FAE was found to be end-product-inhibited. Characterization of the properties of the enzyme
showed that FAE exhibited an activity optimum pH at 6 with pH stability between pH 6 and 8. The optimum temperature was 50 °C
while the temperature stability was between 30 °C and 40 °C, with rapid inactivation at 60 °C and above. The characteristics
and stability of FAE from S. avermitilis CECT 3339 suggest a potential role for this enzyme in combination with endoxylanases for the upgrading of plant-residue silage
and for biopulping.
Received: 17 November 1997 / Received revision: 13 March 1998 / Accepted: 13 April 1998 相似文献
12.
In our previous studies, the yeast Endomyces fibuliger LU677 was found to degrade amygdalin in bitter apricot seeds. The present investigation shows that E. fibuliger LU677 produces extracellular β-glycosidase activity when grown in malt extract broth (MEB). Growth was very good at 25 °C
and 30 °C and slightly less at 35 °C. When grown in MEB of pH 5 and pH 6 with addition of 0, 10 or 100 ppm amygdalin, E. fibuliger produced only slightly more biomass at pH 5, and was only slightly inhibited in the presence of amygdalin. Approximately,
60% of the added amygdalin was degraded (fastest at 35 °C) during an incubation period of 5 days. Supernatants of cultures
grown at 25 °C and pH 6 for 5 days were tested for the effects of pH and temperature on activity (using amygdalin, linamarin
and prunasin as substrates). Prunase activity had two pH optima (pH 4 and pH 6), amygdalase and linamarase only one each at
pH 6 and pH 4–5 respectively. The linamarase activity evolved earlier than amygdalase (2 days and 4 days respectively). The
data thus indicate the presence of at least two different glycosidases having different pH optima and kinetics of excretion.
In the presence of amygdalin, lower glycosidase activities were generally produced. However, the amygdalin was degraded from
the start of the growth, strongly indicating an uptake of amygdalin by the cells. The temperature optimum for all activities
was at 40 °C. Activities of amygdalase (assayed at pH 4) and linamarase (at pH 6) evolving during the growth of E. fibuliger were generally higher in cultures grown at 25 °C and 30 °C. TLC analysis of amygdalin degradation products show a two-stage
sequential mechanism as follows: (1) amygdalin to prunasin and (2) prunasin to cyanohydrin.
Received: 16 September 1997 / Received revision: 6 October 1997 / Accepted: 14 October 1997 相似文献
13.
D. C. La Grange I. S. Pretorius W. H. van Zyl 《Applied microbiology and biotechnology》1997,47(3):262-266
A genomic DNA library of the bacterium Bacillus pumilus PLS was constructed and the β-xylosidase gene (xynB) was amplified from a 3-kb genomic DNA fragment with the aid of the polymerase chain reaction technique. The amplified xynB gene was inserted between the yeast alcohol dehydrogenase II gene promoter (ADH2
P
) and terminator (ADH2
T
) sequences on a multicopy episomal plasmid (pDLG11). The xynB gene was also fused in-frame to the secretion signal sequence of the yeast mating pheromone α-factor (MFα1
S
) before insertion between the ADH2
P
and ADH2
T
sequences on a similar multicopy episomal plasmid (pDLG12). The resulting construct ADH2
P
-MFα1
S
-xynB-ADH2
T
was designated XLO1. Both plasmids pDLG11 and pDLG12 were introduced into Saccharomyces cerevisiae but only the expression of the XLO1 gene yielded biologically functional β-xylosidase. The total β-xylosidase activity remained cell-associated with a maximum
activity of 0.09 nkat/ml obtained when the recombinant S. cerevisiae strain was grown for 143 h in synthetic medium. The temperature and pH optima of the recombinant Xlo1 enzyme were 45–50 °C
and pH 6.6 respectively. The enzyme was thermostable at 45 °C; however, at 60 °C most of the Xlo1 was inactive after 5 min.
Received: 11 July 1996 / Received revision: 23 October 1996 / Accepted: 25 October 1996 相似文献
14.
H. E. M. Mc Mahon C. T. Kelly W. M. Fogarty 《Applied microbiology and biotechnology》1997,48(4):504-509
The α-amylase of Streptomyces sp. IMD 2679 was subject to catabolite repression. Four different growth rates were achieved when the organism was grown
at 40 °C and 55 °C in the presence and absence of cobalt, with an inverse relationship between α-amylase production and growth
rate. Highest α-amylase yields (520 units/ml) were obtained at the lowest growth rate (0.062 h−1), at 40 °C in the absence of cobalt, while at the highest growth rate (0.35 h−1), at 55 °C in the presence of cobalt, α-amylase production was decreased to 150 units/ml. As growth rate increased, the rate
of specific utilisation of the carbon source maltose also increased, from 46 to 123 μg maltose (mg biomass)−1 h−1. The pattern and levels of α-glucosidase (the enzyme degrading maltose) detected intracellularly in each case, indicate that
growth rate effectively controls the rate of feeding of glucose to the cell, and thus catabolite repression.
Received: 17 February 1997 / Received revision: 29 April 1997 / Accepted: 11 May 1997 相似文献
15.
Mesophilic and thermophilic anaerobic digestion of source-sorted organic wastes: effect of ammonia on glucose degradation and methane production 总被引:5,自引:0,他引:5
The wet organic fraction of household wastes was digested anaerobically at 37 °C and 55 °C. At both temperatures the volatile
solids loading was increased from 1 g l−1 day−1 to 9.65 g l−1 day−1, by reducing the nominal hydraulic retention time from 93 days to 19 days. The volatile solids removal in the reactors at
both temperatures for the same loading rates was in a similar range and was still 65% at 19 days hydraulic retention time.
Although more biogas was produced in the thermophilic reactor, the energy conservation in methane was slightly lower, because
of a lower methane content, compared to the biogas of the mesophilic reactor. The slightly lower amount of energy conserved
in the methane of the thermophilic digester was presumably balanced by the hydrogen that escaped into the gas phase and thus
was no longer available for methanogenesis. In the thermophilic process, 1.4 g/l ammonia was released, whereas in the mesophilic
process only 1 g/l ammonia was generated, presumably from protein degradation. Inhibition studies of methane production and
glucose fermentation revealed a K
i (50%) of 3 g/l and 3.7 g/l ammonia (equivalent to 0.22 g/l and 0.28 g/l free NH3) at 37 °C and a K
i (50%) of 3.5 g/l and 3.4 g/l ammonia (equivalent to 0.69 g/l and 0.68 g/l free NH3) at 55 °C. This indicated that the thermophilic flora tolerated at least twice as much of free NH3 than the mesophilic flora and, furthermore, that the thermophilic flora was able to degrade more protein. The apparent ammonia
concentrations in the mesophilic and in the thermophilic biowaste reactor were low enough not to inhibit glucose fermentation
and methane production of either process significantly, but may have been high enough to inhibit protein degradation. The
data indicated either that the mesophilic and thermophilic protein degraders revealed a different sensitivity towards free
ammonia or that the mesophilic population contained less versatile protein degraders, leaving more protein undegraded.
Received: 26 March 1997 / Received revision: 13 May 1997 / Accepted: 19 May 1997 相似文献
16.
The effects of temperature on photosynthesis of a rosette plant growing at ground level, Acaena cylindrostachya R. et P., and an herb that grows 20–50 cm above ground level, Senecio formosus H.B.K., were studied along an altitudinal gradient in the Venezuelan Andes. These species were chosen in order to determine
– in the field and in the laboratory – how differences in leaf temperature, determined by plant form and microenvironmental
conditions, affect their photosynthetic capacity. CO2 assimilation rates (A) for both species decreased with increasing altitude. For Acaena leaves at 2900 m, A reached maximum values above 9 μmol m−2 s−1, nearly twice as high as maximum A found at 3550 m (5.2) or at 4200 m (3.9). For Senecio leaves, maximum rates of CO2 uptake were 7.5, 5.8 and 3.6 μmol m−2 s−1 for plants at 2900, 3550 and 4200 m, respectively. Net photosynthesis-leaf temperature relations showed differences in optimum
temperature for photosynthesis (A
o.t.) for both species along the altitudinal gradient. Acaena showed similar A
o.t. for the two lower altitudes, with 19.1°C at 2900 m and 19.6°C at 3550 m, while it increased to 21.7°C at 4200 m. Maximum
A for this species at each altitude was similar, between 5.5 and 6.0 μmol m−2 s−1. For the taller Senecio, A
o.t. was more closely related to air temperatures and decreased from 21.7°C at 2900 m, to 19.7°C at 3550 m and 15.5°C at 4200 m.
In this species, maximum A was lower with increasing altitude (from 6.0 at 2900 m to 3.5 μmol m−2 s−1 at 4200 m). High temperature compensation points for Acaena were similar at the three altitudes, c. 35°C, but varied in Senecio from 37°C at 2900 m, to 39°C at 3550 m and 28°C at 4200 m. Our results show how photosynthetic characteristics change along
the altitudinal gradient for two morphologically contrasting species influenced by soil or air temperatures.
Received: 5 July 1997 / Accepted: 25 October 1997 相似文献
17.
Cerrutti P Segovia de Huergo M Galvagno M Schebor C del Pilar Buera M 《Applied microbiology and biotechnology》2000,54(4):575-580
The effects of vacuum-drying and freeze- drying on the cell viability of a commercial baker's yeast, Saccharomyces cerevisiae, strain with different endogenous contents of trehalose were analyzed. An osmotolerant Zygosaccharomyces rouxii strain was used for comparative purposes. Higher viability values were observed in cells after vacuum-drying than after freeze-drying.
Internal concentrations of trehalose in the range 10–20% protected cells in both dehydration processes. Endogenous trehalose
concentrations did not affect the water sorption isotherm nor the T
g values. The effect of external matrices of trehalose and maltodextrin was also studied. The addition of external trehalose
improved the survival of S. cerevisiae cells containing 5% internal trehalose during dehydration. Maltodextrin (1.8 kDa) failed to protect vacuum-dried samples
at 40 °C. The major reduction in the viability during the freeze-drying process of the sensitive yeast cells studied was attributed
to the freezing step. The suggested protective mechanisms for each particular system are vitrification and the specific interactions
of trehalose with membranes and/or proteins. The failure of maltodextrins to protect cells was attributed to the fact that
none of the suggested mechanisms of protection could operate in these systems.
Received: 6 December 1999 / Received revision: 8 May 2000 / Accepted: 19 May 2000 相似文献
18.
Production of high yields of arachidonic acid in a fed-batch system by Mortierella alpina ATCC 32222
Of six strains of Mortierella tested, Mortierella alpina ATCC 32222 produced the highest yields of arachidonic acid. Supplementation of soy flour (1% w/v) and vegetable oils (1%
v/v) significantly increased the biomass, lipid content and arachidonic acid level. Replacement of NaNO3 with corn steep liquor (1% w/v) also improved arachidonic acid production. A fed-batch culture system at 25 °C, producing
a high biomass (52.4 g/l) and arachidonic acid content (9.1 g/l) in 8␣days, was developed. A fed-batch system at low temperature
(15 °C) gave even higher arachidonic acid levels (11.1 g/l) in 11 days.
Received: 28 October 1996 / Received revision: 3 March 1997 / Accepted: 7 March 1997 相似文献
19.
Two thermophilic anaerobic bacterial consortia (ALK-1 and LLNL-1), capable of degrading the aromatic fuel hydrocarbons, benzene,
toluene, ethylbenzene, and the xylenes (BTEX compounds), were developed at 60 °C from the produced water of ARCO'S Kuparuk
oil field at Alaska and the subsurface water at the Lawrence Livermore National Laboratory gasoline-spill site, respectively.
Both consortia were found to grow at 45–75 °C on BTEX compounds as their sole carbon and energy sources with 50 °C being the
optimal temperature. With 3.5 mg total BTEX added to sealed 50-ml serum bottles, which contained 30 ml mineral salts medium
and the consortium, benzene, toluene, ethylbenze, m-xylene, and an unresolved mixture of o- and p-xylenes were biodegraded by 22%, 38%, 42%, 40%, and 38%, respectively, by ALK-1 after 14 days of incubation at 50 °C. Somewhat
lower, but significant, percentages of the BTEX compounds also were biodegraded at 60 °C and 70 °C. The extent of biodegradation
of these BTEX compounds by LLNL-1 at each of these three temperatures was slightly less than that achieved by ALK-1. Use of
[ring-14C]toluene in the BTEX mixture incubated at 50 °C verified that 41% and 31% of the biodegraded toluene was metabolized within
14 days to water-soluble products by ALK-1 and LLNL-1, respectively. A small fraction of it was mineralized to 14CO2. The use of [U-14C]benzene revealed that 2.6%–4.3% of the biodegraded benzene was metabolized at 50 °C to water-soluble products by the two
consortia; however, no mineralization of the degraded [U-14C]benzene to 14CO2 was observed. The biodegradation of BTEX at all three temperatures by both consortia was tightly coupled to sulfate reduction
as well as H2S generation. None was observed when sulfate was omitted from the serum bottles. This suggests that sulfate-reducing bacteria
are most likely responsible for the observed thermophilic biodegradation of BTEX in both consortial cultures.
Received: 12 July 1996 / Received revision: 31 December 1996 / Accepted: 31 January 1997 相似文献
20.
C. J. Baxter N. Magan B. Lane H. G. Wildman 《Applied microbiology and biotechnology》1998,49(3):328-332
A Phoma sp., known to produce the pharmaceutically active metabolites squalestatin 1 (S1) and squalestatin 2 (S2), was cultured on
malt-extract/agar (MEA) over a range of water activities (a
w, 0.995–0.90) and temperatures (10–35 °C) to investigate the influence on growth and metabolite production. Use of the ionic
solute NaCl to adjust a
w resulted in significantly lower (P < 0.01) squalestatin yields than when the Phoma sp. was grown on MEA amended with the non-ionic solute glycerol. Water activity and temperature and their interactions were
highly significant factors (P < 0.001) affecting growth of the Phoma sp., with optimum conditions of 0.998–0.980 a
w and 25 °C. Squalestatin production was similarly influenced by a
w, temperature, time and their interactions (P < 0.001). S1 and S2 production occurred over a narrower a
w and temperature range than growth, with a slightly lower optimum a
w range of 0.995–0.980 a
w. The optimum temperature for squalestatin production varied from 20 °C (S1) to 25 °C (S2) and yields of S2 were up to 1000
times lower than those of S1. The ratio of S1 and S2 produced by the Phoma sp. was influenced by a
w and temperature, with highest values at 0.99–0.98 a
w, and at 15 °C. Incubation times of 28 days gave highest yields of both S1 and S2. Up to 2000-fold increases in squalestatin
yields were measured at optimum environmental conditions, compared to the unmodified MEA. This indicates the need to consider
such factors in screening systems used to detect biologically active lead compounds produced by fungi.
Received: 2 June 1997 / Received last revision: 6 November 1997 / Accepted: 7 November 1997 相似文献