Proposed Design Improvement In Process Flow and Form Of Process Change Request at PT. ABC

PT. ABC is a corporation in the automotive manufacturing industry. In corporation's production, PT. ABC supplies goods from several suppliers. Quality management of suppliers and supply goods is needed by PT. ABC to obtain supplies according to the standards set by PT. ABC. The Process Change Request (PCR) is a requisite process for the standard change of supply items covering 4M (man, machine, method, and material). The process flow and form of Process Change Request have been standardized and listed on the Supplier Quality Assurance Manual (SQAM). The Supplier Quality Assurance Manual (SQAM) is the requirement document as a guide to the quality of parts and components, a corporation's internal quality assurance, and a policy for suppliers. In the process flow and form of PCR has been found a problem of inconsistency between the ideal time and the actual time of the PCR's approval phase which hampered the supply of PT. ABC caused by waste. In this study, the researcher proposed the improvement design to the process flow and form of PCR by applying the kaizen concept approach (continuous improvement) using the "plan" step of The PDCA cycle method (plan-do-action) and the fishbone diagram

Optimalisasi Kalsium Karbonat dari Cangkang Telur untuk Produksi Pasta Komposit

Hasil dari penelitian yang telah dilakukan bahwa kandungan kalsium karbonat pada cangkang telur ayam ras yaitu 92,57% dan kalsium yaitu 28%. Sedangkan berat optimum serbuk cangkang untuk pembuatan pasta komposit yaitu 3 gram dengan perbandingan 3,0 (Ca) : 7,0 (BS), dimana pH yang diperoleh yaitu 9. Hal ini sesuai ketentuan SNI bahwa nilai pH untuk pasta komposit yaitu 4,5–10,5. Dan bentuknya semi padat

RANCANGAN USULAN PERBAIKAN PADA ALUR PROSES DAN FORMULIR PCR (PROCESS CHANGE REQUEST) DI PT. XYZ

PT. XYZ is an automotive manufacturing industry. In productivity, PT. XYZ supplied the products of several suppliers. Therefore, it requires a measure of quality assurance for suppliers and supply items so that PT. XYZ may obtain more items according to the established standards. Process Change Request (PCR) is the application for standard supply change on components such as 4M (Man, Machine, Method, Material). The process grooves and PCR forms are standardized and listed on the SQAM (Supplier Quality Manual Assurance). Supplier Quality Assurance Manual (SQAM) is associated with ISO 9001 about its quality management and process systems. The flow of processes and PCR forms has been found a problem of misalignment between the ideal time and the actual time of implementation of the PCR phase, which has slowed down the supply of PT. XYZ. In the study a plan to improve the process flow and PCR forms by applying the kaizen concept approach (continuous improvement) using PDCA (Plan-Do-Check-Action) methods step plan and fishbone diagram

Is consanguinity prevalence decreasing in Saudis?: A study in two generations

Background: Saudi population is unique in that there is a strong  preference for cousin marriages in the general population. We studied the prevalence of consanguinity in educated Saudi females and compared the results with the results obtained in their parents, to access if a generation difference in which extensive educational activities have prevailed to inform the people of the influence of cousin marriages on health, has made any difference in prevalence of consanguineous marriages.Method: A total of 600 Saudi women (421 university students and 179 women attending outpatients’ clinics) were interviewed about their own and their parents’ consanguinity.Results: The total consanguinity (first and second cousins) was 29.7% in the parents. Consanguinity was significantly higher among the daughters than the parents, where 37.9% of the 293 married women had  consanguineous marriages. The prevalence of consanguinity was studied in different age groups, though no significant pattern was observed. A strong correlation was found between consanguinity of parents and their  daughters; consanguinity was highest (52.3%) in the daughters of parents who were themselves consanguineous.Conclusion: The results did not reveal any decrease in the prevalence of consanguinity over a generation. This shows that the tradition of marrying within the family is a preferred practice, despite the awareness that certain genetic disorders occur at a higher frequency in cousin marriages. There is a need at the primary health care level to inform the public of the consequences of this common practice.Key words: Consanguinity; Saudis; First cousin marriage; second cousin marriage; Middle East

Genetic Polymorphisms in Aromatase (CYP19) Gene and Cancer

Estrogens play an important role in the development and progression of several types of cancers. The synthesis of estrogens occurs in almost all tissues of the body in addition to the gonads. The enzyme aromatase (CYP19A1) encoded by CYP19A1 gene is involved in the synthesis of estrogens. Genetic variations in CYP19A1 gene influence both the structure-function relationship of the enzyme and the rate of its synthesis. Extensive studies have reported different types of polymorphisms in the CYP19A1 gene and have shown that the polymorphisms, depending on their location in the gene, have different effects on the function and activity of the gene product. Association studies have been conducted and have led to the realization that interpopulation differences are widespread. Not only do polymorphic forms exert different effects on the development of different cancers, due possibly to the influence of other genetic variations, environmental, metabolic, and epigenetic factors, but also are important as they lead to the interindividual differences seen during treatment of the cancer state. This chapter covers important aspects of the aromatase function, the CYP19A1 gene structure, polymorphisms identified in the gene, different cancers and associated polymorphisms, and the role of the polymorphic forms in affecting the treatment strategies

Human G6PD variant structural studies: Elucidating the molecular basis of human G6PD deficiency

Glucose-6-phosphate dehydrogenase deficiency is by far the most prevalent human enzymopathy and is gener�ated by a series of point mutations in the X-linked gene encoding G6PD. The severity of the deficiency relies on the various mutational sites in the gene, affecting the protein structure and function in at least two ways: by disrupting the entire protein fold or by altering the functional groups. Thus, the modified enzyme should be identified structurally and functionally to recognize the sequelae of each mutation. Understanding the molecular basis of G6PD deficiency is also essential to determine how mutations influence enzyme structure, stability, and activity. In characterizing 34 G6PD variants selected from Class I, II, and III, we reviewed and compared structural and molecular characterizations. These studies have shown that these mutations can influence the G6PD enzyme's local and global stability by changing the features of the mutant amino acids or by modifying their interactions (lost, increased, or decreased distances). Furthermore, the relationship between the changes in the enzyme structure and the severity of the disease was also reviewed. Overall, their results showed that Class I had the strongest influence on the protein's stability, activity, and function, which correlated with chronic non�spherocytic hemolytic anemia. Furthermore, there have been no drugs available to treat G6PD deficiency until now

In Silico Analysis of Single Nucleotide Polymorphism (SNPs) in Human β-Globin Gene

Single amino acid substitutions in the globin chain are the most common forms of genetic variations that produce hemoglobinopathies- the most widespread inherited disorders worldwide. Several hemoglobinopathies result from homozygosity or compound heterozygosity to beta-globin (HBB) gene mutations, such as that producing sickle cell hemoglobin (HbS), HbC, HbD and HbE. Several of these mutations are deleterious and result in moderate to severe hemolytic anemia, with associated complications, requiring lifelong care and management. Even though many hemoglobinopathies result from single amino acid changes producing similar structural abnormalities, there are functional differences in the generated variants. Using in silico methods, we examined the genetic variations that can alter the expression and function of the HBB gene. Using a sequence homology-based Sorting Intolerant from Tolerant (SIFT) server we have searched for the SNPs, which showed that 200 (80%) non-synonymous polymorphism were found to be deleterious. The structure-based method via PolyPhen server indicated that 135 (40%) non-synonymous polymorphism may modify protein function and structure. The Pupa Suite software showed that the SNPs will have a phenotypic consequence on the structure and function of the altered protein. Structure analysis was performed on the key mutations that occur in the native protein coded by the HBB gene that causes hemoglobinopathies such as: HbC (E→K), HbD (E→Q), HbE (E→K) and HbS (E→V). Atomic Non-Local Environment Assessment (ANOLEA), Yet Another Scientific Artificial Reality Application (YASARA), CHARMM-GUI webserver for macromolecular dynamics and mechanics, and Normal Mode Analysis, Deformation and Refinement (NOMAD-Ref) of Gromacs server were used to perform molecular dynamics simulations and energy minimization calculations on β-Chain residue of the HBB gene before and after mutation. Furthermore, in the native and altered protein models, amino acid residues were determined and secondary structures were observed for solvent accessibility to confirm the protein stability. The functional study in this investigation may be a good model for additional future studies

The Gln27Glu Polymorphism in β2-Adrenergic receptor gene is linked to hypertriglyceridemia, hyperinsulinemia and hyperleptinemia in Saudis

<p>Abstract</p> <p>Background</p> <p>β2-adrenoceptor (β2AR) gene polymorphism glutamine 27 glutamic acid (Gln27Glu) and Arg16Gly were reported to have an association with obesity and obesity related disorders in some population. We evaluated Gln27Glu polymorphism in the β2AR gene in obese Saudi populations to investigate the association of β2AR gene with obesity and other related metabolic parameters.</p> <p>Design</p> <p>We studied possible association of Gln27Glu in β2AR gene with body mass index (BMI), anthropometric measurements and other metabolic parameters. The β2AR gene polymorphism (Gln27Glu) was identified by sequencing PCR products representing locus of interest. Based on BMI, the subjects were divided into three groups, normal weight, overweight and obese. The genotype and allele frequency were calculated separately for each group.</p> <p>Results</p> <p>The allelic frequency of Glu27 did not differ amongst the three groups, though the Glu27 homozygote (Glu/Glu) were more in obese subjects and had higher concentration of triglyceride, leptin and insulin compared to in the Gln27 heterozygotes and Gln/Gln homozygotes.</p> <p>Conclusions</p> <p>In this study we were able to provide evidence on the influence of Gln27Glu genetic variant of β2AR gene on lipid phenotypes, insulin and leptin levels in the Saudi populations.</p

Interleukin (IL)-17A and IL-17F and asthma in Saudi Arabia: mRNA transcript levels and gene polymorphisms

Asthma is a multifactorial disorder and both genetic and environmental factors contribute to its development. The present study explored cytokines interleukin (IL)-17A and IL17F levels as usable parameters for the diagnosis of asthmatics Saudi patients. Blood samples were collected from 100 asthma patients and 100 matched controls. The transcript mRNA levels in whole blood were determined by real-time reverse-transcription polymerase chain reaction. Expression studies showed that levels of IL17A and IL17F were significantly higher in asthma patients compared to controls [IL17A: 1.112 (2.088) vs 0.938 (1.363)]; IL17F: 0.707 (1.33) vs 0.667 (0.590). The mRNA transcripts of IL17A and IL17F were positively and significantly correlated in all subjects examined in this study: controls as well as asthma patients (r = 0.455, P &lt; 0.01 for controls and r = 0.644, P &lt; 0.01 for patients). These findings suggest that asthma is characterized by an elevation of cytokines IL17A and IL17F and the measurement of their expression can be a valuable parameter for the diagnosis of asthma.Keywords: Asthma, interleukin-17F (IL17F), interleukin-17A (IL17A), gene expression, real time-polymerase chain reaction (RT-PCR), Saudi Arabia.African Journal of Biotechnology Vol. 12(23), pp. 3615-362