Abstract: Disclosed herein are metabolically engineered cells capable of producing carotenoids from acid whey.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having a partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having at partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having a partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: Disclosed are: a method for detecting common wheat among from wheat varieties contained in a sample of interest such as a food raw material or a processed food specifically, with high sensitivity, and in a qualitative and/or quantitative manner; a method for discriminating between common wheat and a wheat variety other than common wheat (e.g., durum wheat) contained in a food raw material or a processed food and detecting the common wheat in a qualitative and/or quantitative manner; and a primer set, a nucleic acid probe, and a detection kit, each of which can be used in the methods employing a PCR method.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having at partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having a partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: Disclosed are: a method for detecting common wheat among from wheat varieties contained in a sample of interest such as a food raw material or a processed food specifically, with high sensitivity, and in a qualitative and/or quantitative manner; a method for discriminating between common wheat and a wheat variety other than common wheat (e.g., durum wheat) contained in a food raw material or a processed food and detecting the common wheat in a qualitative and/or quantitative manner; and a primer set, a nucleic acid probe, and a detection kit, each of which can be used in the methods employing a PCR method.

Abstract: Provided is a method of detecting or quantifying a wheat species-specific DNA in a test sample by polymerase chain reaction. The method comprises a step of amplifying a nucleic acid molecule having a partial sequence of a nucleotide sequence identified as SEQ ID NO: 1 using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as the template and using a primer pair capable of amplifying the partial sequence and a step of detecting or quantifying the amplified nucleic acid molecule.

Abstract: A path (different power-supply path) in which verification objective paths pass through two or more power domains is searched from a netlist and power-supply information, and delay-coefficient additional determination is performed in the different power-supply path. In this step, from voltage conditions in each power domain, a voltage condition under which the timing analysis result is most negative is detected, it is determined whether or not the delay coefficient is added for the voltage condition, and the delay coefficient is added. When the delay coefficient is added, the delay coefficient obtained in consideration of the power-supply voltage variation for the delay of the cell belonging to the different power-supply path is extracted from the delay-coefficient information, and is added to the delay value calculated based on the library. Then, based on the delay value to which the delay coefficient is added, the static timing verification is performed.

Abstract: The improved version of a chromated metal sheet has a chromate layer on at least one side of a metal substrate or a plated metal substrate and it is characterized in that the chromate layer has a chromium deposit of 10-200 mg/m.sup.2 per surface in terms of metallic Cr, that the chromate layer contains silica in an amount of 0.1-6.0 in terms of the weight ratio of SiO.sub.2 to Cr, and that the chromate layer contains at least one kind of lubricating particles selected from the group consisting of graphite, MoS.sub.2, BN, calcium stearate and an organic lubricating substance in an amount of 0.1-100 in terms of the weight ratio of the lubricating particles to Cr. The lubricating particles can have a surface layer capable of nonionic surface activating action, and this surface layer accounts for 1-70 wt % of the lubricating particles.

Abstract: The present invention aims to obtain C-Si-Mn-Cr system of hot-rolled dual phase structured steel sheets having a low yield ratio YR of not greater than 65%, an excellent strength-elongation balance M, a low variation in quality and an excellent cold formability through stepwise cooling regulation in the course of cooling from the final rolling to coiling.The present invention is a method for producing hot-rolled steel sheets having a low yield ratio and a high tensile strength due to dual phase structure by effecting the final rolling of a hot-rolled steel sheet containing 0.02-0.2% of C, 0.05-2.0% of Si, 0.5-2.0% of Mn and 0.3-1.5% of Cr as the essential components at a temperature of finishing the final rolling of 780.degree. C., rapidly cooling the thus treated steel sheet at a cooling rate of more than 40.degree. C./S to the temperature range wherein the transformation of .gamma. into .alpha.