Biosynthesis of PP-V, a monascorubramine homologue, by Penicillium sp. AZ

The biosynthetic pathway of PP-V, a new monascorubramine homologue, was elucidated by ¹³C-labeling studies. The [1-¹³C] of acetate was incorporated into 2-, 3a-, 4a-, 6-, 8-, 9-, 11-, 13-, 15-, 17-, and 19-Cs of PP-V, and the [2-¹³C], into 3-, 4-, 5-, 8a-, 9a-, 10-, 12-, 14-, 16-, 18-, and 20-Cs. These incorporation patterns coincide with those reported in the biosynthesis of a Monascus azaphilone pigment, monascorubrin.     

Effect of ammonium nitrate on the production of PP-V and monascorubrin homologues by Penicillium sp. AZ

A fungal strain, Penicillium sp. AZ, has been found to produce the monascorubramine homologues, PP-V [(10Z)-3-(9a-methyl-3-octanoyl-2,9-dioxo-2,7,9,9a-tetrahydro-furo[3,2-g]isoquinolin-6-yl)-acrylic acid] and PP-R [(10Z)-7-(2-hydroxyethyl)-monascorubramine] when cultured in a medium composed of soluble starch, ammonium nitrate, yeast extract, and citrate buffer, pH 5.0. When ammonium nitrate was omitted from the culture medium, PP-V and PP-R production was replaced by orange (PP-O) and yellow-orange (PP-Y) pigment production. The structures of these pigments were determined by FAB-MS and 1H and 13C NMR to be novel compounds, (10Z)-3-(9a-methyl-3-octanoyl-2,9-dioxo-9,9a-dihydro-2H-furo[3,2-g]isochromen-6-yl)-acrylic acid and (10Z)-monascorubrin, respectively.     

Production and structural analysis of PP-V, a homologue of monascorubramine, produced by a new isolate of Penicillium sp

A fungal strain newly isolated from soil has been found to produce a violet water-soluble pigment (PP-V) in high quantity when cultured in a medium consisting of soluble starch and citrate buffer. Glucose repressed the production of this pigment. PP-V has the molecular formula C23H25NO6 revealed by HR-FAB mass spectroscopy and has been shown to be composed of an isoquinoline skeleton, a n-octanoyl group, and a 2-propenoic acid group by NMR. In conclusion, PP-V is a novel compound, 3-(9a-methyl-3-octanoyl-2,9-dioxo-2,7,9,9a-tetrahydro-furo[3,2-g]isoquinolin-6-yl)acrylic acid; a homologue of monascorubramine in which the 1-propenyl group is converted to a 2-propenoic acid group.     

PP-R, 7-(2-hydroxyethyl)-monascorubramine, a red pigment produced in the mycelia of Penicillium sp. AZ

A red pigment was extracted and purified from the mycelia of a newly isolated strain of Penicillium sp., Penicillium sp. AZ, which produced a soluble violet pigment PP-V, 12-carboxyl-monascorubramine, in the culture fluid. The red pigment, PP-R, was determined by FAB-MS and 1H and 13C NMR to be a novel compound, 7-(2-hydroxyethyl)-monascorubramine.     

Atmospheric chemistry of perfluoroalkanesulfonamides: kinetic and product studies of the OH radical and Cl atom initiated oxidation of N-ethyl perfluorobutanesulfonamide

Perfluorooctanesulfonamides [C8F17SO2N(R1)(R2)] are present in the atmosphere and may, via atmospheric transport and oxidation, contribute to perfluorocarboxylates (PFCA) and perfluorooctanesulfonate (PFOS) pollution in remote locations. Smog chamber experiments with the perfluorobutanesulfonyl analogue N-ethyl perfluorobutanesulfonamide [NEtFBSA; C4F9SO2N(H)CH2CH3] were performed to assess this possibility. By use of relative rate methods, rate constants for reactions of NEtFBSA with chlorine atoms (296 K) and OH radicals (301 K) were determined to be kCL) = (8.37 +/- 1.44) x 10(-12) and kOH = (3.74 +/- 0.77) x 10(-13) cm3 molecule(-1) s(-1), indicating OH reactions will be dominant in the troposphere. Simple modeling exercises suggestthat reaction with OH radicals will dominate removal of perfluoroalkanesulfonamides from the gas phase (wet and dry deposition will not be important) and that the atmospheric lifetime of NEtFBSA in the gas phase will be 20-50 days, thus allowing substantial long-range atmospheric transport. Liquid chromatography/tandem mass spectrometry (LC/MS/MS) analysis showed that the primary products of chlorine atom initiated oxidation were the ketone C4F9SO2N(H)COCH3; aldehyde 1, C4F9SO2N(H)CH2CHO; and a product identified as C4F9SO2N(C2H5O)- by high-resolution MS but whose structure remains tentative. Another reaction product, aldehyde 2, C4F9SO2N(H)CHO, was also observed and was presumed to be a secondary oxidation product of aldehyde 1. Perfluorobutanesulfonate was not detected above the level of the blank in any sample; however, three perfluoroalkanecarboxylates (C3F7CO2-, C2F5CO2-, and CF3CO2-) were detected in all samples. Taken together, results suggest a plausible route by which perfluorooctanesulfonamides may serve as atmospheric sources of PFCAs, including perfluorooctanoic acid.     

甜菜多倍体新品种双丰309的选育

甜菜多倍体新品种双丰309由四倍体双丰416的3个系号与二倍体双丰8号杂交育成，属于工艺品质优良的标准型多粒种多倍体品种。其糖汁纯度较对照品种双丰8号提高3～6个百分点，α-氨基氮含量低27．2％，钠含量低16％，糖份回收率提高5个百分点。该品种在黑龙江省甜菜品区域试验及生产示范中，其平均块根产量、含糖率和产糖量比统一对照品种双丰8号（CK）提高10．9～11．5％、0．21～0．44度和12．9～14．3％。在全国甜菜品种区域试验中，块根产量比当地对照品种提高13．3％，含糖率提高0．6度，产糖量提高18．9％。     

Vascular sources of phenylalanine, tyrosine, lysine, and methionine for casein synthesis in lactating goats

The contribution to casein biosynthesis of peptides derived from blood was examined in late lactation goats (254 to 295 d in milk). Ratios of mammary uptake of free amino acids (AA) in blood to output of AA in milk protein and ratios of the enrichments of Phe, Tyr, Met, and Lys at isotopic plateau in secreted milk casein to the free AA in arterial and mammary vein blood were monitored during the last 5 h of a 30-h continuous i.v. infusion of [1-13C]Phe, [2H4]Tyr, [5-13CH3]Met, and [2-15N]Lys on two occasions: before (control) and on d 6 of an i.v. infusion of Phe (6 g/d). During the control, uptakes of free Phe and Met were less than their output in milk. This result was comparable with the labeling kinetic results, suggesting that vascular peptides contributed 5 to 11% of Phe and 8 to 18% of Met. Free Tyr and Lys uptakes during the control were sufficient for milk output; however, the labeling kinetics indicated that 13 to 25% of the Tyr and 4 to 13% of the Lys were derived from peptides. Infusion of Phe increased the uptake of free AA but reduced the contribution of peptides toward Phe (0 to 3%) and Tyr (8 to 14%) supply for casein synthesis. Whole body hydroxylation of Phe to Tyr increased from 10 to 18% with the infusion of Phe; within the mammary gland, this conversion was lower (3 to 5%). Results suggest that the mammary utilization of peptides containing Phe and Tyr appears to depend on the supply of free AA in blood.     

Cover Image,Volume 97, Issue 12

The cover image, by Wai Chin Li and Chin Fung Chow, is based on the Review Adverse child health impacts resulting from food adulterations in the Greater China Region, DOI: 10.1002/jsfa.8405 .

     

Effect of root zone pH and form and concentration of nitrogen on accumulation of quality‐related components in green tea

Green tea quality is greatly influenced by concentrations of free amino acids, polyphenols (mainly catechins) and caffeine. The present study investigated the principal relationship between selected nutritional factors (form and concentration of N supply, root zone pH) and accumulation of these quality‐related components of tea (Camellia sinensis (L.)) plants. Tea plants were hydroponically cultured with NH , NO and NH NO at pH 4.0, 5.0 and 6.0 in one experiment and supplied with varying N concentrations (0.75, 2.0 and 4.5 mmol L^?1, NH /NO^?₃ = 3:1) in another experiment. Concentrations of free amino acids were considerably higher in NH ‐ than in NO ‐fed plants. This was attributed to the much greater absorption of NH compared with NO . Furthermore, the relative allocation of absorbed N to free amino acids, particularly theanine and glutamine, was substantially increased by NH nutrition, suggesting that NH was more readily assimilated than NO into theanine. The concentration of caffeine was increased in NH ‐ and (NH NO )‐supplied plants, whereas concentrations of catechins were reduced in (NH NO )‐fed plants. Root zone pH did not influence concentrations of most free amino acids in young shoots, with the exception of theanine, which increased at low pH (4.0) irrespective of N form; this likely stemmed from an accumulation effect, as growth decreased more strongly than N absorption. Raising the N supply increased plant N allocation to free amino acids. The increase was most striking for arginine, while theanine was only marginally affected. This may have adverse consequences for green tea quality, as less favourable taste characteristics have been attributed to arginine. Copyright © 2007 Society of Chemical Industry     

Cover Image,Volume 97, Issue 11

The cover image, by Hannah C Wells et al., is based on the Research Article Deer leather: analysis of the microstructure affecting pebble, DOI: 10.1002/jsfa.8199 .

     

Lipid oxidation. Part V. Effect of copper on the autoxidation of methyl oleate

Methyl oleate was oxidized at 60°C at free access of air in presence of varying amounts of copper(II)-chloride. Changes of hydroperoxides followed equation (V): . The relationships between the two reaction rate constants and the concentration of copper(I1)ions are best expressed by hyperbolic equations (VII) and VIII, respectively: . The relation between the concentration of copper and the time necessary to attain the maximum rate of increase of the hydroperoxide content was hyperbolic as well. The rate of the hydroperoxide formation increases thus with the increasing content of copper chloride but the rate of hydroperoxide decomposition becomes still more rapid at the same time so that the accumulation of hydroperoxides is inhibited in case of extremely high concentrations of copper.     

Cover Image,Volume 99, Issue 13

The cover image is based on the Research Article Study of the physical and chemical changes during the maturation of three cocoa clones, EET8, CCN51, and ICS60 by Andrés F Cubillos Bojacá et al., DOI: 10.1002/jsfa.9882 . Cover image ©AGROSAVIA Images.

     

Influence of freezing method on thaw drip and protein loss of low-voltage electrically stimulated and non-stimulated sheeps' muscle

South African Mutton Merino wethers (n = 32) were slaughtered, yielding carcasses with a mean weight of 22·18 ± 2·11 kg. Sixteen carcasses were electrically stimulated (ES) (21 V, 60 Hz, 120 s) immediately and all carcasses were chilled at room temperature (16°C) for 3 h and then overnight at 4°C, 95% RH. Both left and right Mm. longissimus lumborum et thoracis were excised and cut into six portions (77 g ± 7·8 g), each placed separately in a polyethylene bag and randomly allocated to five freezing treatments. These were: (1) cryogenic, -65°C; (2) cryogenic, -90°C; (3) walk-in-freezer, -21°C; (4) blast freezer, -21°C; (5) domestic freezer, -25°C. The respective freezing rates were 4·4, 6·4, 0·55, 0·35 and 0·51 cm h(-1) to -2·2°C at core depth of 1 cm below the surface. Samples were frozen to core temperatures of -20°C, removed and placed in a storage freezer (-20°C) for 48 h and 2·5 months. Samples were then suspended in perforated bags in a chiller (4°C) to thaw, and drip was collected in outer bags over the periods 0-24, 24-48, 48-72 and 72-96 h and expressed as g (100 g)(-1). Freezing methods had significant (P < 0·01) influences on drip loss in both ES and NES samples. Following storage for 48 h post-freezing at -20°C, total drip (g (100 g)(-1)) over 96 h of both ES and NES samples for the five freezing treatments were respectively: (1) 7·61 and 4·61; (2) 7·35 and 3·29; (3) 9·44 and 4·68; (4) 9·07 and 5·43; (5) 10·58 and 5·15. Following storage for 2·5 months, the total ES and NES drip were respectively, (1) 11·25 and 9·38; (2) 10·36 and 9·15; (3) 13·72 and 12·65; (4) 13·70 and 12·26; (5) 11·92 and 11·29. Total protein in the drip did not differ between freezing treatments. Differences between ES and NES samples did occur in the 48 h storage group. It is concluded that cryogenic freezing results in less thaw drip than the vapour compression systems. This advantage of cryogenic freezing disappears if meat is stored for long periods at -20°C. Electrical stimulation increases the drip loss in samples frozen for 48 h, but the differences are not significant after 2·5 months frozen storage. Protein losses parallel the drip.     

PRINCIPAL FATTY ACIDS OF LIPID CLASSES FROM FRESH WATER FISH (CALLICHROUS PABDA)

The body lipids of a fresh water fish were separated into classes and subclasses. The nonpolar lipid class was separated into seven different subclasses. The fatty acid composition of triacylglycerols, sterol esters and free fatty acids were determined. A substantial amount of C20:4n-6 (AA), typical of tropical water fish, was present. In addition to other fatty acids common in fresh water fish, short-chain saturated fatty acids, namely C8:0, C10:0 and odd-chain fatty acids C13:0, C13:1, C17:0, C17:1 and C19:0 were detected in relatively large proportions. The principal fatty acids were C14:0, C16:0, C16:1, C18:0, C18:1, C18:2n-6, C18:3n-3, C20:4n-6, C20:5n-3 and C22:6n-3. The patterns of fatty acid distribution within lipid classes showed general similarities.     

Sodium Lactate Effects on Shelf-Life, Sensory, and Physical Characteristics of Fresh Pork Sausage

The objective of our study was to evaluate the effects of various levels (0%, 1%, 2%, 3%) of sodium lactate on selected physical, sensory, and microbiological characteristics of fresh pork sausage stored at 4°C for 28 days. Samples containing 0% and 1% SL reached 10⁸ CFU/g after 10 days refrigerated storage. Addition of 2% or 3% SL to fresh pork sausage delayed microbial deterioration, pH decline, and development of sour- and off-flavors 7 days at 4°C. Samples containing 2% SL did not reach total plate counts of 10⁸ CFU/g until 24 days storage. SL appeared to protect red color, and to “enhance” pork-and salty-flavors in sausage. TBA, L-, a-, and b-values were unaffected by SL level.     

蔗渣膳食纤维化学结构的研究(Ⅳ)──挤压蒸煮对化学结构的影响

蔗渣细胞壁物质（膳食纤维）整体的化学成分与单糖组成不随双螺杆挤压蒸煮而发生变化。细胞壁物质中80℃H2O分级组分的相对含量会因挤压蒸煮处理而由原来的24％提高到13．3％，且分子的Xyl：Ara比值由原来的6．2减小到4．2；1mol／LNaOH分级组分的相对含量则由原来的189％减少到11．2％，分子Xal：Ara比值由原来9．3增加至11．4。挤压蒸煮对这2种分级组分的聚合物基本结构没有影响，但会使lmol／LNaOH分级组分发生增溶作用或断裂部分连接键，导致其分子量下降，分子更趋于直线型，分支程度减小，其中有部分转变成80℃H2O分级组分。     

Effects of different transition diets on dry matter intake,milk production,and milk composition in dairy cows

The primary objective of this study was to evaluate the effect on dry matter intake (DMI), milk yield, milk composition, body weight (BW), and body condition score (BCS) change of cows offered diets differing in energy density in the last 4 wk of gestation and in the first 8 wk of lactation. Three diets (grass silage:straw, 75:25 on a dry matter basis (SS), grass silage (S), and grass silage + 3 kg concentrate daily (C)) precalving, and two diets (4 kg [LC] or 8 kg [HC] concentrate daily + grass silage ad libitum) postcalving were combined in a 3 x 2 factorial design. Sixty Holstein-Friesian cows entering their second lactation were blocked according to expected calving date and BCS into groups of six and were then allocated at random to the treatments. Individual feeding started 4 wk prior to the expected calving date and measurements were made until the end of the 8th wk of lactation. Mean DMI differed between each of the precalving treatments (7.4, 8.1, and 9.9 kg/d for SS, S, and C, respectively) in the precalving period. The DMI also differed between SS and C for wk 1 to 8 (13.5 and 14.2 kg/d) postcalving. Postcalving, milk (24.2, 26.2, and 28.2 kg/d), fat (933, 1063, and 1171 g/d), and protein (736, 797, and 874 g/d) yields differed between SS, S, and C, respectively. The BCS changes differed between SS and C (-0.09 and 0.12 of a BCS) in the precalving period and between SS and S compared with C (0.02, 0.06, and -0.26 of a BCS) for wk 1 to 8 postcalving. The BW change differed between SS and S compared with C in both wk 1 to 4 (-0.23, -0.37, and -1.25 kg/d) and wk 1 to 8 (0.18, 0.10, and -0.58 kg/ d) postcalving. The BW and BCS were lower at calving for cows on SS compared with C. The greater amount of concentrate supplement postcalving increased DMI, yields of milk, fat, and protein and decreased BW loss in the first 8 wk of lactation. In conclusion, these results indicate that a greater energy density diet in the final 4 wk of the dry period improves cow production in early lactation.     

Effect of chemical form,heating, and oxidation products of linoleic acid on rumen bacterial population and activities of biohydrogenating enzymes

Heating polyunsaturated fatty acids (PUFA) produces oxidation products, such as hydroperoxides, aldehydes, and oxypolymers, which could be responsible at least in part for modification of PUFA rumen biohydrogenation (BH). Three in vitro experiments were conducted to investigate the effects of linoleic acid (cis-9,cis-12-C18:2) oxidation products on BH. In the first experiment, we studied the effects of free linoleic acid (FLA), heated FLA (HFLA, at 150°C for 6 h), triacylglycerols of linoleic acid (TGLA), heated TGLA (HTGLA, at 150°C for 6 h), 13-hydroperoxide (13HPOD), trans-2-decenal (T2D), and hexanal (HEX) on BH in vitro after 6 and 24 h of incubation. In the second experiment, aldehydes differing in chain length and degree of unsaturation [pentanal, HEX, heptanal, nonanal, T2D, trans-2,trans-4-decadienal (T2T4D)] were incubated in vitro for 5 h in rumen fluid. In the third experiment, 9-hydroperoxide (9HPOD), 13HPOD, HEX, or T2T4D were incubated for 1 h in rumen fluid inactivated with chloramphenicol to investigate their effects on enzyme activity. In experiment 1, heat treatment of TGLA generated TGLA oxypolymers, did not affect cis-9,cis-12-C18:2 disappearance, but did decrease BH intermediates, especially trans-11 isomers. Heating FLA decreased cis-9,cis-12-C18:2 disappearance and cis-9,trans-11-CLA and trans-11-C18:1 production. Treatment with HEX and T2D did not affect cis-9,cis-12-C18:2 disappearance and barely affected production of BH intermediates. The bacterial community was affected by 13HPOD compared with FLA and HFLA, in parallel with an increase in trans-10 isomer production after a 6-h incubation. After 24 h of incubation, 13HPOD decreased trans-11 isomer production, but to a lesser extent than HFLA. In experiment 2, some weak but significant effects were observed on BH, unrelated to chain length or degree of unsaturation of aldehydes; the bacterial community was not affected. In experiment 3, 9HPOD inhibited Δ⁹-isomerization, and both 9HPOD and 13HPOD inhibited Δ¹²-isomerization. We concluded that oxypolymers did not affect cis-9,cis-12-C18:2 disappearance. Heating both esterified and free cis-9,cis-12-C18:2 greatly altered Δ¹²-isomerization. Aldehydes had few effects. Hydroperoxides are responsible, at least in part, for the effects of fat heating: 13HPOD increased trans-10 isomer production (probably by affecting the bacterial community) and decreased trans-11 isomer production by inhibiting Δ¹²-isomerase activity, whereas 9HPOD inhibited both isomerases.     

Dissolution of various sources of gypsum in aqueous solutions and in soil

The dissolution of six sources of gypsum in water and 0.01 M CaCl₂ was examined in the presence and absence of soil. The gypsum samples included: analytical grade (AR), three sources of flue-gas desulphurisation (FGD) gypsum, phosphogypsum (PG), and mined gypsum (MG). Dissolution in aqueous solutions was monitored by measuring the concentration of calcium (Ca²⁺) and sulphate (SO) ions. In soils which adsorb small amounts of SO^?2₄, dissolution was estimated from the increase in the concentration of Ca²⁺ and SO in gypsum-treated soil over the control soil. However, in soils which adsorb significant amounts of SO, measurement of solution SO concentration underestimates the extent of dissolution. Gypsum dissolution was larger in water (15.20 mmol litre^?1) than in 0.01 M CaCl₂ (11.12 mmol litre^?1), and this was attributed to the Ca²⁺ common-ion effect. The rate of dissolution decreased in the order: AR > FGD > PG > MG. Dissolution was 2 to 10 times faster for powdered (< 500 .m) gypsum than for the discs obtained by pelletising. The differences in the rate of dissolution between the gypsum sources and between powder and disc samples were related to both surface area and the presence of CaCO₃, impurity. The rate of dissolution was 3 to 8 times faster in the presence than in the absence of soil. Whereas the dissolution of gypsum in the presence of soil followed first order reaction kinetics, it followed second order kinetics in the absence of soil. This difference in reaction kinetics resulted from the continuous removal of Ca2+ and SO by the soil.