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Ernawati Puji Rahayu
"Metode Taqman MGB real time PCR yang cepat merupakan kunci pengawasan pemalsuan daging yang efektif. Penelitian bertujuan mengevaluasi kuantitas, kualitas DNA produk olahan daging babi, serta kandungan DNA babi produk olahan daging sapi yang diduga mengandung babi menggunakan Taqman MGB real time PCR untuk memverifikasi label. Lima produk olahan daging babi, 30 produk olahan daging sapi: dendeng, abon, baso, dan daging asap sebagai sampel, serta daging babi segar sebagai kontrol positif diekstraksi, diukur konsentrasi, kemurnian DNA, dielektroforesis serta diamplifikasi dengan realtime PCR. Konsentrasi, kemurnian DNA, nilai Ct sampel diuji ANAVA satu arah dilanjutkan uji Tukey, kecuali nilai Ct produk olahan daging sapi. Integritas DNA genomnya dianalisis deskriptif. Hasil uji ANAVA menunjukkan ada pengaruh nyata (P˂0,05) konsentrasi, kemurnian DNA dan nilai Ct. Hasil uji Tukey produk olahan daging babi: ada beda nyata konsentrasi DNA sampel dan kontrol positif (P˂0,05), kecuali kornet (P˃0,05). Kemurnian DNA baso dan daging asap berbeda nyata (P˂0,05) dengan kontrol positif. Nilai Ct sampel dan kontrol positif berbeda nyata (P˂0,05), kecuali dendeng (P˃0,05). Hasil uji Tukey produk olahan daging sapi: konsentrasi DNA baso dan daging asap berbeda nyata (P<0,05) dengan kontrol positif, kemurnian DNA kornet berbeda nyata (P<0,05) dengan kontrol positif. Semua DNA genom sampel terfragmentasi ukuran terendahnya sekitar 250 bp dimiliki kornet dan abon. Produk olahan daging dapat meningkat kuantitas DNAnya dan menurun kualitas DNAnya tergantung pada suhu dan bahan tambahan yang diberikan. Tiga puluh produk olahan daging sapi tidak mengandung DNA babi menggunakan Taqman real time PCR yang sensitif dan cepat serta terverifikasi mematuhi peraturan label.

The fast Taqman MGB qPCR method is key to effective meat adulteration surveillance. This research aimed to evaluate the quantity, quality of DNA from processed pork products and the content of pork DNA in processed beef products suspected of containing pork DNA using the Taqman MGB qPCR to verify labels. Five processed pork products, 30 processed beef products: corned, jerky, shredded, meatballs, and smoked meat were used as samples as well as and fresh pork as a positive control were extracted, DNA concentration and purity were measured, electrophoresed, and amplified with qPCR. The DNA concentration, purity, and Ct value were tested by one-way ANOVA followed by the Tukey test, except for the Ct value of processed beef products. The genomic DNA integrity was analyzed descriptively. The ANOVA showed a significant effect (P˂0.05) on the concentration and purity of DNA and Ct value. Tukey test results for processed pork products: there was a significant difference (P˂0.05) in the DNA concentration of the samples and positive controls, except for corned (P˃0.05). The DNA purity of pork meatballs and smoked pork was significantly different (P˂0.05) from the positive control. The Ct values of the samples and positive control were significantly different (P˂0.05), except for jerky (P˃0.05). The results of the Tukey test for processed beef products: the DNA concentration of beef meatballs and smoked beef was significantly different (P<0.05) with the positive control, and the DNA purity of corned beef was significantly different (P<0,05) with positive control. All genomic DNA samples were fragmented with the smallest size of about 250 bp experienced by corned and shredded. Processed meat products can increase the quantity of DNA and decrease the quality depending on temperature and additives. Thirty processed beef products did not contain pork DNA using the sensitive and fast Taqman qPCR and verified to comply with label regulations."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2022
T-pdf
UI - Tesis Membership  Universitas Indonesia Library
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Lawrie, R.A.
Jakarta: UI-Press, 1995
641.3 LAW mt
Buku Teks  Universitas Indonesia Library
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"[Daging sintetik dengan bahan baku gluten terigu, tepung kacang merah, jamur tiram putih, dan rumput laut dengan variasi komposisi massa jamur dan rumput laut telah selesai dilakukan. Daging sintetik terbaik memiliki komposisi 68% gluten; 13,5% tepung kacang merah; 4% ISP; 4,5% kuning telur; 2% jamur; dan 8% rumput laut. Hasil analisis proksimat dengan kadar protein tertinggi dimiliki oleh sampel A[2,8] sebesar 34,4%. Hasil uji TPA (Texture Profile Analysis) daging memiliki daya kohesiv sebesar 0,747g (gaya); kekerasan daging 5578g; dan elastisitas 92g. Sedangkan hasil pengujian organoleptik menunjukkan bahwa responden menilai kemiripan daging sintetik dengan daging hewani mengenai rasa sampel memperoleh nilai 61,8% menyerupai daging hewani; 80,6% untuk wujud; 68,2% untuk kekenyalan; dan aroma sebesar 62,8%. Peningkatkan kualitas daging dapat ditingkatkan dengan kombinasi bahan nabati lainnya., Synthethic Meat with main ingredients of gluten, red bean flour, white oyster mushroom, and seaweed with variation of mushrooom and seaweed composition has been done. The best composition of the meat has 68% of gluten; 13.5% red bean flour; 4% ISP; 4.5% yolk; 2% mushroom; and 8% seaweed.
Best proximate analysis with the highest protein content is sampel A[2,8] with value of 34.4%. For Texture Profile Analysisis, cohessiveness of meat is 0.747g (force); hardness 5578g; and elastisity 92g. While the organoleptic test results the meat resemblance has taste 61.8% like meat; 80.6% for form; 68.2% plasticity; and 62.8% for aroma. Improvement of synthethic meat can be made by new variation of other natural ingredients.]"
Fakultas Teknik Universitas Indonesia, 2014
S58838
UI - Skripsi Membership  Universitas Indonesia Library
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Tiara Jasmine
"Kasus kontaminasi daging haram seperti babi hutan (Sus scrofa) dan babi domestik (Sus scrofa domesticus) dalam makanan yang beredar di Indonesia menyebabkan perlu dilakukannya verifikasi halal. Pengaplikasian real-time PCR telah mempermudah proses verifikasi halal untuk mendeteksi kandungan DNA babi sebab metode tersebut memiliki tingkat sensitivitas yang tinggi. Studi analisis sekuensing gen 12S rRNA terdahulu menunjukkan bahwa gen 12S rRNA dapat membedakan spesies hewan yang berkerabat dekat sehingga gen tersebut memiliki potensi sebagai gen target dalam studi deteksi halal. Namun, adanya kekurangan pada desain primer pada studi deteksi halal sebelumnya mendorong perlu dilakukannya penelitian lebih lanjut terkait potensi primer gen 12S rRNA sebagai dasar pengembangan halal kit. International Organization of Standardization (ISO) telah menetapkan metode standar untuk deteksi babi, yaitu ISO/TS 20224-3:2020(E) menggunakan primer Porcine-97 bp sebagai primer standar yang spesifik terhadap gen ACTB pada Sus scrofa. Penelitian ini bertujuan untuk merancang primer spesifik terhadap gen 12S rRNA Sus scrofa, menganalisis sensitivitas dan spesifisitas primer rancangan dalam mendeteksi gDNA babi, serta mengevaluasi potensi primer rancangan untuk dijadikan sebagai primer alternatif dalam deteksi halal. Penelitian ini dilakukan dengan merancang primer menggunakan gen 12S rRNA sebagai gen target. Primer 12S rRNA (SS12S-120bp) divalidasi dengan menganalisis spesifisitas secara in silico dan menguji sensitivitas primer menggunakan metode real-time PCR. Analisis perbandingan kualitatif antara primer 12S rRNA dengan primer ACTB ISO juga telah dilakukan. Uji sensitivitas dan linieritas dilakukan dengan melakukan dilusi bertingkat terhadap gDNA babi pada konsentrasi 10.000, 1000, 100, 10, 5, dan 1 pg/uL sebanyak 2 replikat. Hasil validasi spesifisitas in silico menunjukkan bahwa primer 12S rRNA (forward: 5’-GGT CCT GGC CTT TCT ATT AAT TCT TAA-3’; reverse: 5’-CCG TTA TAG GTG TGC TTG ATA CC-3’; dan probe: 5’-[FAM]-CCC GGT GAG AAT GCC CTC CAG ATC-[BHQ1]-3’) bersifat spesies spesifik terhadap gen 12S rRNA Sus scrofa. Analisis qPCR menunjukkan bahwa primer 12S rRNA dapat mendeteksi gDNA babi hingga konsentrasi paling rendah, yaitu 1 pg/uL dengan suhu 56 derajat celcius sebagai suhu optimal annealing primer. Nilai efisiensi dan nilai linieritas yang diperoleh adalah 85% dan 0,995. Berdasarkan analisis perbandingan yang telah dilakukan, dapat disimpulkan bahwa primer 12S rRNA bersifat lebih sensitif dan spesies spesifik dalam mendeteksi gDNA babi dibandingkan dengan primer ACTB ISO.

Cases of haram meat contamination such as wild boar (Sus scrofa) and domestic pig (Sus scrofa domesticus) in foods circulating in Indonesia cause the need for halal verification. The application of real-time PCR has facilitated halal verification process to detect the content of pig DNA down to the smallest concentration. The 12S rRNA gene has previously been used in several species identification studies and is known to have potential as a target gene in halal detection studies. However, some deficiencies in the primer design from the previous research prompted the need for further research regarding the potential of the 12S rRNA gene primers as the basis for halal kit development. ISO/TS 20224-3:2020(E) has established primer Porcine-97 bp as the standard primer used to detect the ACTB gene in Sus scrofa. This study aims to design a specific primer for the 12S rRNA Sus scrofa gene, analyze the sensitivity and specificity of the designed primer in detecting pig gDNA, and evaluate the potential of the designed primer to serve as an alternative primer for halal detection. This research was done by designing primers using Sus scrofa 12S rRNA gene as the target gene. Designed 12S rRNA primers (SS12S-120bp) was validated by analyzing in silico specificity and primer sensitivity test using real-time PCR method. Qualitative comparisons between 12S rRNA and ACTB ISO primers was also analyzed. Sensitivity test was carried out by conducting serial dilution of porcine gDNA at 10,000, 1000, 100, 10, 5, and 1 pg/uL in duplicates. In silico specificity results showed that the designed 12S rRNA primer (forward: 5’-GGT CCT GGC CTT TCT ATT AAT TCT TAA-3’; reverse: 5’-CCG TTA TAG GTG TGC TTG ATA CC-3’; and probe: 5’-[FAM]-CCC GGT GAG AAT GCC CTC CAG ATC- [BHQ1]-3’) was species specific to 12S rRNA Sus scrofa gene. qPCR analysis showed that 12S rRNA primer could detect pig gDNA down to the lowest concentration of 1 pg/uL at 56 degree celcius as its optimum annealing temperature. The efficiency and linearity value obtained was 85% and 0,995. Based on the conducted qualitative comparison analysis, it can be concluded that primer 12S rRNA is more sensitive and species specific in detecting pig gDNA compared to ACTB ISO primer."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2023
S-pdf
UI - Skripsi Membership  Universitas Indonesia Library
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"[Daging sintetik merupakan salah satu alternatif pilihan makanan yang dapat
menggantikan daging hewani dengan tingkat protein yang tidak kalah tinggi.
Kandungan protein yang tinggi dapat diperoleh dari berbagai bahan organik
seperti gluten dari tepung terigu, jamur tiram putih (Pleurotus ostreatus), dan
tepung kacang merah. Pembuatan daging sintetik dilakukan dengan variasi bahan
baku, yaitu tepung jamur dan jamur yang dicincang; serta variasi konsentrasi.
Penentuan jenis daging sintetik terbaik dilakukan dengan analisis proksimat, asam
amino, dan organoleptik. Daging sintetik terbaik diperoleh dari kombinasi 70%
gluten, 15% tepung kacang merah, dan 15% tepung jamur tiram putih dengan
kadar protein sebesar 29,7%; kadar air 48,05%; kadar abu 1,680%; kadar lemak
2,480%; dan kadar karbohidrat 18,05%. Terdapat 15 jenis asam amino yang
terkandung dalam daging sintetik, diantaranya adalah aspartat, glutamat, serin,
glisin, histidin, arginin, threonin, alanin, prolin, valin, tirosin, isoleusin, leusin,
phenylalanin, lisin. Sedangkan hasil pengujian organoleptik menunjukkan bahwa
responden menilai kemiripan daging sintetik dengan daging hewani mengenai
rasa sebesar 67,5%; kekenyalan 66,0%; aroma 73,5%; dan wujud 90,5%., Synthetic meat is one of the alternative food choices that can replace animal meat
with the same amount of protein content. High protein content can be obtained
from a variety of organic materials such as gluten from wheat flour, white oyster
mushroom (Pleurotus ostreatus), and red bean flour. In this research,
manufacturing process of synthetic meat is divided into two types, the first type
use mushroom flour and the second type use chopped mushroom as its raw
material. Every type of synthetic meat manufactured in different variety of
concentration. The best synthetic meat is determined by using proximate analysis,
amino acid analysis, and organoleptic analysis. The best synthetic meat derived
from a combination of 70% gluten, 15% red bean flour and 15% of white oyster
mushroom flour with a protein content of 29.7%; moisture content of 48.05%; ash
content of 1.680%; fat content of 2.480%; and carbohydrate content of 18.05%.
There are 15 types of amino acids contained in the synthetic meat, such as
aspartate, glutamate, serine, glycine, histidine, arginine, threonine, alanine,
proline, valine, tyrosine, isoleucine, leucine, phenylalanin, lysine. While the
organoleptic test results showed that the respondents assess similarity synthetic
meat with animal flesh about the taste of 67.5%; elasticity of 66.0%; scent of
73.5%; and form of 90.5%. ash content]"
Fakultas Teknik Universitas Indonesia, 2014
S57228
UI - Skripsi Membership  Universitas Indonesia Library
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Nadya Rishelin
"ABSTRAK
Konsumsi daging diperkirakan meningkat dalam dekade mendatang secara global. Sebagian besar bahan baku untuk produk makanan di Indonesia berasal dari daging yang akan mendorong permintaan daging tinggi. Daging merupakan salah satu produk yang didinginkan (cold chain) sehingga lebih sensitif terhadap kontaminasi dengan bakteri dan non halal. Bagian downstream pada supply chain daging di Indonesia terdiri dari logistik, grosir, dan pengecer. Indonesia masih minim dalam penelitian penilaian kriteria untuk sertifikasi halal supply chain pada bagian downstream. Penelitian ini berfokus pada kriteria penilaian halal supply chain daging di bagian downstream Indonesia. Tahap pertama dalam penelitian yaitu penentuan risiko berdasarkan literatur dan kemudian validasi oleh ahli. Selanjutnya, penelitian ini menggunakan metode DEMATEL based ANP untuk mendapatkan rincian urutan risiko halal supply chain daging. Penentuan kriteria penilaian dari validasi oleh ahli didapatkan setelah mendapatkan urutan risiko. Temuan penelitian ini menunjukkan bahwa ada 48 risiko yang diidentifikasi, 28 risiko untuk kriteria penilaian dan 44 kriteria penilaian halal supply chain daging pada bagian downstream di Indonesia.

ABSTRACT
Meat consumption is expected to increase in the next decade globally. Most of the ingredients of food products in Indonesia are meat, especially beef, which will drive a high-level demand for meat. Meat is one of the cold products, known as a cold chain that is more sensitive to bacteria and non-halal contamination. The downstream sector of the meat supply chain in Indonesia consists of logistics, wholesalers, and retailers. Indonesia still has minimal of halal supply chain research in the assessment of criteria for halal supply chain certification in the downstream sector. This study focuses on halal supply chain certification in the Indonesian downstream sector. The first stage is the determination of risk based on the literature and then expert validation. Furthermore, this study uses the DEMATEL based ANP method to get the ranking of halal meat supply chain risk. Determination of assessment criteria based on expert is obtained after getting the ranking of halal meat supply chain risk. The findings of this study are 48 identified risks, 28 risks for assessment criteria, and 44 assessment criteria of the halal supply chain in Indonesia."
Depok: Fakultas Teknik Universitas Indonesia , 2020
T-Pdf
UI - Tesis Membership  Universitas Indonesia Library
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Artikel Jurnal  Universitas Indonesia Library
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Monica Winata Nurtanio
"ABSTRAK
Konsumsi daging yang berlebihan memiliki dampak negatif bagi sebagian masyarakat Indonesia karena kolesterol yang tinggi dan harga yang mahal. Namun daging masih menjadi pilihan untuk dikonsumsi karena belum ada alternatif daging sehat. Daging nabati dibuat sebagai salah satu solusi bagi masyarakat yang ingin mengonsumsi daging yang sehat, hanya saja di Indonesia masih didominasi oleh produk impor. Penelitian ini membahas tentang pra perancangan produk daging nabati sapi dan ayam dengan merk Meat-Up untuk memenuhi kebutuhan di Jabodetabek. Bahan baku yang digunakan adalah gluten, kacang merah, kedelai, TVP, dan bumbu untuk daging nabati sapi, dan gluten, singkong, kedelai, TVP, dan bumbu untuk daging nabati ayam. Pabrik direncanakan beroperasi pada pertengahan tahun 2017. Pabrik akan dibangun di Bogor karena akses untuk mendapatkan bahan baku produk lebih mudah. Sistem produksi yang diterapkan adalah batch. Kapasitas produksi pabrik adalah 94 ton per tahun. Alat produksi utama yang digunakan ada 10, yaitu washer, weighing scale, miller, chopper, mixer, extruder, steamer, cooker, slicer, dan vacuum packaging machine. Total investasi yang diperlukan untuk membangun pabrik ini adalah Rp. 2.659.270.125. Adapun nilai ROI-nya adalah 32,9%, dengan PBP 2,36 tahun, MARR 17%, IRR 38%, BEP 32,3%, NPV Rp. 5.607.340.158. Harga jual yang ditetapkan untuk produk daging nabati Meat-Up adalah Rp. 30.000. Dengan demikian, pabrik Meat-Up sangat layak dibangun karena menguntungkan

ABSTRACT
High consumption of meat has a negative effect for some people in Indonesia due to its high cholestrol and expensive price. However meat still becomes a common choice for daily consumption because there is no alternative healthier meat. Gluten-based vegetarian meat was made as a solution for people who want to eat meat in healthy way, but in Indonesia imported products are still dominating the market. This study discusses the preliminary production design of vegetable beef and chicken meat with Meat-Up brands to meet the needs in the Greater Jakarta. The raw materials used are gluten, red beans, soybeans, TVP, and vegetable seasoning for vegetable beef meat, and gluten, cassava, soybean, TVP, and seasoning for vegetable chicken meat. The plant will be operated in mid 2017. The plant will be built in Bogor due to accessibility to raw materials. The production system applied is batch. The production capacity is 94 tons per year. The main production equipment used are 10 equipment, which are washer, weighing scale, miller, chopper, mixer, extruder, steamer, cooker, slicer, and vacuum packaging machine. The total investment required to build this plant is Rp. 2,659,270,125. The value of its ROI is 32.9%, with PBP 2.36 years, MARR 17%, IRR 38%, 32.3% BEP, NPV Rp. 5,607,340,158. The sale price set for this vegetable meat products is Rp. 30,000. Thus, Meat-Up plant is very feasible to be built because it is profitable."
2016
T45760
UI - Tesis Membership  Universitas Indonesia Library
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Virgyanka Nayla
"Perkembangan teknologi menyebabkan praktik pencampuran produk makanan menggunakan substansi non-halal. Dokumen (International Standardization Organization/ Technical Specification) ISO/TS 20224-3: 2020 digunakan sebagai prosedur standar uji deteksi kehalalan berbasis Deoxyribonucleic Acid (DNA) memanfaatkan metode Quantitative Polymerase Chain Reaction (qPCR) yang berlaku secara internasional melalui gen Beta actin (ACTB) sebagai gen target. Namun, kemampuan gen ACTB sebagai gen target belum banyak teruji langsung melalui reaksi PCR sehingga dibutuhkan evaluasi potensi gen target alternatif lain melalui optimasi primer seperti gen Cytochrome b (Cytb) untuk mendeteksi kandungan babi domestik (Sus scrofa domesticus) dan babi hutan (Sus scrofa). Metode yang digunakan terdiri atas desain primer dan probe, optimasi suhu annealing primer dan probe, uji spesifisitas in silico, uji sensitivitas in vitro, serta pengolahan dan analisis data. Adapun sampel yang digunakan untuk uji sensitivitas in vitro adalah pig genomic DNA. Berdasarkan pengujian yang dilakukan, primer dan probe gen Cytb memiliki suhu annealing optimal pada suhu 55°C. Uji spesifisitas in silico membuktikan bahwa sekuens primer dan probe gen Cytb memiliki kemampuan deteksi pada sekuens babi domestik dan babi hutan. Uji sensitivitas menggunakan qPCR pada gen ACTB membentuk kurva standar dengan nilai y=-3,6541x +38,385 dan R2=0,9967, serta LoD sebesar 5 pg/uL. Nilai linearitas (0,9967) dan efisiensi (87,78%) yang dihasilkan masuk ke dalam rentang standar sesuai literatur karena berada ≥0,98 untuk linearitas dan rentang 80%—120% untuk efisiensi. Sementara itu, uji sensitivitas menggunakan qPCR pada gen Cytb membentuk kurva standar dengan nilai y=-2,7222x + 32,196 dan R2= 0,9867, serta LoD sebesar 1 pg/uL. Nilai linearitas (0,9867) yang dimiliki masuk ke dalam rentang standar, tetapi nilai efisiensi (132,99%) melebihi rentang persentase yang baik akibat kemungkinan konsentrasi serial dilusi yang kurang sesuai dan protokol yang belum optimal. Gen Cytb memiliki jangkauan sensitivitas yang lebih baik dibandingkan gen ACTB. Keseluruhan grafik hasil membentuk kurva sigmoid yang valid sebagai hasil uji qPCR. Oleh karena itu, berdasarkan uji spesifisitas in silico dan sensitivitas in vitro yang dilakukan dapat disimpulkan bahwa gen Cytb berpotensi dijadikan gen target altenatif sebagai pengembangan halal kit.

Technological developments have led to the practice of mixing food products using non-halal substances. Document (International Standardization Organization/Technical Specification) ISO/TS 20224-3: 2020 is used as a standard procedure for Deoxyribonucleic Acid (DNA)-based halal detection test that is internationally applicable through the Beta actin gene (ACTB) as the target gene. However, the ability of the ACTB gene as a target gene has not been tested directly through PCR reactions, so it is required to evaluate the potential of other alternative target genes through primer optimization such as the Cytochrome b (Cytb) gene to detect domestic pig (Sus scrofa domesticus) and wild boar (Sus scrofa) containment. The method used was comprised of primer and probe design, primer and probe annealing temperature optimization, in silico specificity test, in vitro sensitivity test, and data processing and analysis. The sample used for the in vitro sensitivity test is pig genomic DNA. Based on the tests conducted, primers and probes of the Cytb gene have an optimal annealing temperature at 55°C. The in silico specificity test proved that the primer sequences and Cytb gene probes have the ability to detect domestic pig and wild boar sequences. The sensitivity test using qPCR on the ACTB gene forming a standard curve with a value of y=-3.6541x +38.385 and R2=0.9967, and LoD of 5 pg/uL. The linearity (0.9967) and efficiency (87.78%) values generated are in the standard range according to the literature because they are ≥0.98 for linearity and 80%—120% range for efficiency. Meanwhile, the sensitivity test using qPCR on the Cytb gene is forming a standard curve with a value of y= -2.7222x + 32.196 and R2= 0.9867, and LoD of 1 pg/uL. The linearity value (0.9867) is within the standard range, but the efficiency value (132.99%) exceeds the good percentage range as a result of the possibility of inappropriate serial dilution concentrations and an unoptimal protocol. The Cytb gene has a better sensitivity range than the ACTB gene. The overall result graph forms a sigmoid curve which is valid as a qPCR test result. Therefore, based on the in silico specificity and in vitro sensitivity tests, it can be concluded that the Cytb gene has the potential to be used as an alternative target gene as a halal kit development."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2023
S-pdf
UI - Skripsi Membership  Universitas Indonesia Library
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Toldra, Fidel
"The book goal is to summarize the state of the art on the chemical safety issues currently concerning meat and poultry, and to discuss the current international legislation on the tools available for their control. In addition, there will be a discussion of both the substances that may be generated as a consequence of processing, and the tools that are available for their control. Finally, the controls for the detection of foreign proteins (e.g., whey proteins) in the final products will be also compiled.
"
New York: Springer, 2012
e20405794
eBooks  Universitas Indonesia Library
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